For Healthcare Professionals

PrivacyPolicy

Last Updated on July 8th , 2020

1. Our Commitment to Privacy

This platform, defined to include any access via a web browser and any related application (collectively “Platform”), is provided, owned and managed by IQVIA™. IQVIA is committed to protecting your privacy. This Platform is provided by IQVIA for the purposes of supporting your potential or actual participation in one or more clinical trials or other health-related research (“clinical trials”) and the accompanying use and disclosure of your personal information, either as a patient, caregiver or as a member of the study team (PI, Patient Guide, Study Concierge, etc.). This Privacy Policy covers your full engagement with IQVIA current and future clinical trials and other health care- related research, from your initial interaction with the Platform to the beginning of your contact with a potential trial, through participation in any trial and potential participation in other trials and additional uses of your personal information as identified in this Privacy Policy to support medical research. This Privacy Policy describes how we use, disclose and protect any personal information that we collect or receive from you or on your behalf through this Platform, whether as a potential clinical trial or healthcare research participant, patient, data subject or healthcare professional. If you are participating in a specific clinical trial as a trial participant, this Policy supplements the information you have received or will receive as part of the clinical trial’s informed consent process. The informed consent form (“ICF”) and research protocol will define how information about you will be used in connection with the clinical trial. This Policy is intended to meet applicable legal requirements globally, including in North America, Europe, Asia Pacific and other relevant jurisdictions and supplements the IQVIA Privacy Policy and Online Privacy Policy, which can be found at www.IQVIA.com.

Your Role and Responsibilites

  • You should be familiar with how our Platform works and read all our policies.
  • You should be aware of, and have a right to know, what information is collected on this Platform, how it is stored, protected and used.

Your Rights and Choices

  • You have the right to know the information collection and storage practices of this Platform.
  • You have the right to know how your information will be used and by whom.
  • You have the right to know to whom we may disclose your information, the clinical trial and the ICF.

2. The Information we Collect

This platform, defined to include any access via a web browser and any related application (collectively “Platform”), is provided, owned and managed by IQVIA™. IQVIA is committed to protecting your privacy. This Platform is provided by IQVIA for the purposes of supporting your potential or actual participation in one or more clinical trials or other health-related research (“clinical trials”) and the accompanying use and disclosure of your personal information, either as a patient, caregiver or as a member of the study team (PI, Patient Guide, Study Concierge, etc.). This Privacy Policy covers your full engagement with IQVIA current and future clinical trials and other health care- related research, from your initial interaction with the Platform to the beginning of your contact with a potential trial, through participation in any trial and potential participation in other trials and additional uses of your personal information as identified in this Privacy Policy to support medical research. This Privacy Policy describes how we use, disclose and protect any personal information that we collect or receive from you or on your behalf through this Platform, whether as a potential clinical trial or healthcare research participant, patient, data subject or healthcare professional. If you are participating in a specific clinical trial as a trial participant, this Policy supplements the information you have received or will receive as part of the clinical trial’s informed consent process. The informed consent form (“ICF”) and research protocol will define how information about you will be used in connection with the clinical trial. This Policy is intended to meet applicable legal requirements globally, including in North America, Europe, Asia Pacific and other relevant jurisdictions and supplements the IQVIA Privacy Policy and Online Privacy Policy, which can be found at www.IQVIA.com.

Your Role and Responsibilites

  • You should be familiar with how our Platform works and read all our policies.
  • You should be aware of, and have a right to know, what information is collected on this Platform, how it is stored, protected and used.

Your Rights and Choices

  • You have the right to know the information collection and storage practices of this Platform.
  • You have the right to know how your information will be used and by whom.
  • You have the right to know to whom we may disclose your information, the clinical trial and the ICF.

3. Web Logs

This platform, defined to include any access via a web browser and any related application (collectively “Platform”), is provided, owned and managed by IQVIA™. IQVIA is committed to protecting your privacy. This Platform is provided by IQVIA for the purposes of supporting your potential or actual participation in one or more clinical trials or other health-related research (“clinical trials”) and the accompanying use and disclosure of your personal information, either as a patient, caregiver or as a member of the study team (PI, Patient Guide, Study Concierge, etc.). This Privacy Policy covers your full engagement with IQVIA current and future clinical trials and other health care- related research, from your initial interaction with the Platform to the beginning of your contact with a potential trial, through participation in any trial and potential participation in other trials and additional uses of your personal information as identified in this Privacy Policy to support medical research. This Privacy Policy describes how we use, disclose and protect any personal information that we collect or receive from you or on your behalf through this Platform, whether as a potential clinical trial or healthcare research participant, patient, data subject or healthcare professional. If you are participating in a specific clinical trial as a trial participant, this Policy supplements the information you have received or will receive as part of the clinical trial’s informed consent process. The informed consent form (“ICF”) and research protocol will define how information about you will be used in connection with the clinical trial. This Policy is intended to meet applicable legal requirements globally, including in North America, Europe, Asia Pacific and other relevant jurisdictions and supplements the IQVIA Privacy Policy and Online Privacy Policy, which can be found at www.IQVIA.com.

Your Role and Responsibilites

  • You should be familiar with how our Platform works and read all our policies.
  • You should be aware of, and have a right to know, what information is collected on this Platform, how it is stored, protected and used.

Your Rights and Choices

  • You have the right to know the information collection and storage practices of this Platform.
  • You have the right to know how your information will be used and by whom.
  • You have the right to know to whom we may disclose your information, the clinical trial and the ICF.

4. Cookies and Other Technologies

This platform, defined to include any access via a web browser and any related application (collectively “Platform”), is provided, owned and managed by IQVIA™. IQVIA is committed to protecting your privacy. This Platform is provided by IQVIA for the purposes of supporting your potential or actual participation in one or more clinical trials or other health-related research (“clinical trials”) and the accompanying use and disclosure of your personal information, either as a patient, caregiver or as a member of the study team (PI, Patient Guide, Study Concierge, etc.). This Privacy Policy covers your full engagement with IQVIA current and future clinical trials and other health care- related research, from your initial interaction with the Platform to the beginning of your contact with a potential trial, through participation in any trial and potential participation in other trials and additional uses of your personal information as identified in this Privacy Policy to support medical research. This Privacy Policy describes how we use, disclose and protect any personal information that we collect or receive from you or on your behalf through this Platform, whether as a potential clinical trial or healthcare research participant, patient, data subject or healthcare professional. If you are participating in a specific clinical trial as a trial participant, this Policy supplements the information you have received or will receive as part of the clinical trial’s informed consent process. The informed consent form (“ICF”) and research protocol will define how information about you will be used in connection with the clinical trial. This Policy is intended to meet applicable legal requirements globally, including in North America, Europe, Asia Pacific and other relevant jurisdictions and supplements the IQVIA Privacy Policy and Online Privacy Policy, which can be found at www.IQVIA.com.

Your Role and Responsibilites

  • You should be familiar with how our Platform works and read all our policies.
  • You should be aware of, and have a right to know, what information is collected on this Platform, how it is stored, protected and used.

Your Rights and Choices

  • You have the right to know the information collection and storage practices of this Platform.
  • You have the right to know how your information will be used and by whom.
  • You have the right to know to whom we may disclose your information, the clinical trial and the ICF.

5. Device Information

This platform, defined to include any access via a web browser and any related application (collectively “Platform”), is provided, owned and managed by IQVIA™. IQVIA is committed to protecting your privacy. This Platform is provided by IQVIA for the purposes of supporting your potential or actual participation in one or more clinical trials or other health-related research (“clinical trials”) and the accompanying use and disclosure of your personal information, either as a patient, caregiver or as a member of the study team (PI, Patient Guide, Study Concierge, etc.). This Privacy Policy covers your full engagement with IQVIA current and future clinical trials and other health care- related research, from your initial interaction with the Platform to the beginning of your contact with a potential trial, through participation in any trial and potential participation in other trials and additional uses of your personal information as identified in this Privacy Policy to support medical research. This Privacy Policy describes how we use, disclose and protect any personal information that we collect or receive from you or on your behalf through this Platform, whether as a potential clinical trial or healthcare research participant, patient, data subject or healthcare professional. If you are participating in a specific clinical trial as a trial participant, this Policy supplements the information you have received or will receive as part of the clinical trial’s informed consent process. The informed consent form (“ICF”) and research protocol will define how information about you will be used in connection with the clinical trial. This Policy is intended to meet applicable legal requirements globally, including in North America, Europe, Asia Pacific and other relevant jurisdictions and supplements the IQVIA Privacy Policy and Online Privacy Policy, which can be found at www.IQVIA.com.

Your Role and Responsibilites

  • You should be familiar with how our Platform works and read all our policies.
  • You should be aware of, and have a right to know, what information is collected on this Platform, how it is stored, protected and used.

Your Rights and Choices

  • You have the right to know the information collection and storage practices of this Platform.
  • You have the right to know how your information will be used and by whom.
  • You have the right to know to whom we may disclose your information, the clinical trial and the ICF.

6. The way we use your information

This platform, defined to include any access via a web browser and any related application (collectively “Platform”), is provided, owned and managed by IQVIA™. IQVIA is committed to protecting your privacy. This Platform is provided by IQVIA for the purposes of supporting your potential or actual participation in one or more clinical trials or other health-related research (“clinical trials”) and the accompanying use and disclosure of your personal information, either as a patient, caregiver or as a member of the study team (PI, Patient Guide, Study Concierge, etc.). This Privacy Policy covers your full engagement with IQVIA current and future clinical trials and other health care- related research, from your initial interaction with the Platform to the beginning of your contact with a potential trial, through participation in any trial and potential participation in other trials and additional uses of your personal information as identified in this Privacy Policy to support medical research. This Privacy Policy describes how we use, disclose and protect any personal information that we collect or receive from you or on your behalf through this Platform, whether as a potential clinical trial or healthcare research participant, patient, data subject or healthcare professional. If you are participating in a specific clinical trial as a trial participant, this Policy supplements the information you have received or will receive as part of the clinical trial’s informed consent process. The informed consent form (“ICF”) and research protocol will define how information about you will be used in connection with the clinical trial. This Policy is intended to meet applicable legal requirements globally, including in North America, Europe, Asia Pacific and other relevant jurisdictions and supplements the IQVIA Privacy Policy and Online Privacy Policy, which can be found at www.IQVIA.com.

Your Role and Responsibilites

  • You should be familiar with how our Platform works and read all our policies.
  • You should be aware of, and have a right to know, what information is collected on this Platform, how it is stored, protected and used.

Your Rights and Choices

  • You have the right to know the information collection and storage practices of this Platform.
  • You have the right to know how your information will be used and by whom.
  • You have the right to know to whom we may disclose your information, the clinical trial and the ICF.

7. How we may disclose your information

This platform, defined to include any access via a web browser and any related application (collectively “Platform”), is provided, owned and managed by IQVIA™. IQVIA is committed to protecting your privacy. This Platform is provided by IQVIA for the purposes of supporting your potential or actual participation in one or more clinical trials or other health-related research (“clinical trials”) and the accompanying use and disclosure of your personal information, either as a patient, caregiver or as a member of the study team (PI, Patient Guide, Study Concierge, etc.). This Privacy Policy covers your full engagement with IQVIA current and future clinical trials and other health care- related research, from your initial interaction with the Platform to the beginning of your contact with a potential trial, through participation in any trial and potential participation in other trials and additional uses of your personal information as identified in this Privacy Policy to support medical research. This Privacy Policy describes how we use, disclose and protect any personal information that we collect or receive from you or on your behalf through this Platform, whether as a potential clinical trial or healthcare research participant, patient, data subject or healthcare professional. If you are participating in a specific clinical trial as a trial participant, this Policy supplements the information you have received or will receive as part of the clinical trial’s informed consent process. The informed consent form (“ICF”) and research protocol will define how information about you will be used in connection with the clinical trial. This Policy is intended to meet applicable legal requirements globally, including in North America, Europe, Asia Pacific and other relevant jurisdictions and supplements the IQVIA Privacy Policy and Online Privacy Policy, which can be found at www.IQVIA.com.

Your Role and Responsibilites

  • You should be familiar with how our Platform works and read all our policies.
  • You should be aware of, and have a right to know, what information is collected on this Platform, how it is stored, protected and used.

Your Rights and Choices

  • You have the right to know the information collection and storage practices of this Platform.
  • You have the right to know how your information will be used and by whom.
  • You have the right to know to whom we may disclose your information, the clinical trial and the ICF.

8. Access, Correction, Deletion, and Removal of Personal Information

This platform, defined to include any access via a web browser and any related application (collectively “Platform”), is provided, owned and managed by IQVIA™. IQVIA is committed to protecting your privacy. This Platform is provided by IQVIA for the purposes of supporting your potential or actual participation in one or more clinical trials or other health-related research (“clinical trials”) and the accompanying use and disclosure of your personal information, either as a patient, caregiver or as a member of the study team (PI, Patient Guide, Study Concierge, etc.). This Privacy Policy covers your full engagement with IQVIA current and future clinical trials and other health care- related research, from your initial interaction with the Platform to the beginning of your contact with a potential trial, through participation in any trial and potential participation in other trials and additional uses of your personal information as identified in this Privacy Policy to support medical research. This Privacy Policy describes how we use, disclose and protect any personal information that we collect or receive from you or on your behalf through this Platform, whether as a potential clinical trial or healthcare research participant, patient, data subject or healthcare professional. If you are participating in a specific clinical trial as a trial participant, this Policy supplements the information you have received or will receive as part of the clinical trial’s informed consent process. The informed consent form (“ICF”) and research protocol will define how information about you will be used in connection with the clinical trial. This Policy is intended to meet applicable legal requirements globally, including in North America, Europe, Asia Pacific and other relevant jurisdictions and supplements the IQVIA Privacy Policy and Online Privacy Policy, which can be found at www.IQVIA.com.

Your Role and Responsibilites

  • You should be familiar with how our Platform works and read all our policies.
  • You should be aware of, and have a right to know, what information is collected on this Platform, how it is stored, protected and used.

Your Rights and Choices

  • You have the right to know the information collection and storage practices of this Platform.
  • You have the right to know how your information will be used and by whom.
  • You have the right to know to whom we may disclose your information, the clinical trial and the ICF.

9. Your choices

This platform, defined to include any access via a web browser and any related application (collectively “Platform”), is provided, owned and managed by IQVIA™. IQVIA is committed to protecting your privacy. This Platform is provided by IQVIA for the purposes of supporting your potential or actual participation in one or more clinical trials or other health-related research (“clinical trials”) and the accompanying use and disclosure of your personal information, either as a patient, caregiver or as a member of the study team (PI, Patient Guide, Study Concierge, etc.). This Privacy Policy covers your full engagement with IQVIA current and future clinical trials and other health care- related research, from your initial interaction with the Platform to the beginning of your contact with a potential trial, through participation in any trial and potential participation in other trials and additional uses of your personal information as identified in this Privacy Policy to support medical research. This Privacy Policy describes how we use, disclose and protect any personal information that we collect or receive from you or on your behalf through this Platform, whether as a potential clinical trial or healthcare research participant, patient, data subject or healthcare professional. If you are participating in a specific clinical trial as a trial participant, this Policy supplements the information you have received or will receive as part of the clinical trial’s informed consent process. The informed consent form (“ICF”) and research protocol will define how information about you will be used in connection with the clinical trial. This Policy is intended to meet applicable legal requirements globally, including in North America, Europe, Asia Pacific and other relevant jurisdictions and supplements the IQVIA Privacy Policy and Online Privacy Policy, which can be found at www.IQVIA.com.

Your Role and Responsibilites

  • You should be familiar with how our Platform works and read all our policies.
  • You should be aware of, and have a right to know, what information is collected on this Platform, how it is stored, protected and used.

Your Rights and Choices

  • You have the right to know the information collection and storage practices of this Platform.
  • You have the right to know how your information will be used and by whom.
  • You have the right to know to whom we may disclose your information, the clinical trial and the ICF.

10. International transfers

This platform, defined to include any access via a web browser and any related application (collectively “Platform”), is provided, owned and managed by IQVIA™. IQVIA is committed to protecting your privacy. This Platform is provided by IQVIA for the purposes of supporting your potential or actual participation in one or more clinical trials or other health-related research (“clinical trials”) and the accompanying use and disclosure of your personal information, either as a patient, caregiver or as a member of the study team (PI, Patient Guide, Study Concierge, etc.). This Privacy Policy covers your full engagement with IQVIA current and future clinical trials and other health care- related research, from your initial interaction with the Platform to the beginning of your contact with a potential trial, through participation in any trial and potential participation in other trials and additional uses of your personal information as identified in this Privacy Policy to support medical research. This Privacy Policy describes how we use, disclose and protect any personal information that we collect or receive from you or on your behalf through this Platform, whether as a potential clinical trial or healthcare research participant, patient, data subject or healthcare professional. If you are participating in a specific clinical trial as a trial participant, this Policy supplements the information you have received or will receive as part of the clinical trial’s informed consent process. The informed consent form (“ICF”) and research protocol will define how information about you will be used in connection with the clinical trial. This Policy is intended to meet applicable legal requirements globally, including in North America, Europe, Asia Pacific and other relevant jurisdictions and supplements the IQVIA Privacy Policy and Online Privacy Policy, which can be found at www.IQVIA.com.

Your Role and Responsibilites

  • You should be familiar with how our Platform works and read all our policies.
  • You should be aware of, and have a right to know, what information is collected on this Platform, how it is stored, protected and used.

Your Rights and Choices

  • You have the right to know the information collection and storage practices of this Platform.
  • You have the right to know how your information will be used and by whom.
  • You have the right to know to whom we may disclose your information, the clinical trial and the ICF.

11. Information security

This platform, defined to include any access via a web browser and any related application (collectively “Platform”), is provided, owned and managed by IQVIA™. IQVIA is committed to protecting your privacy. This Platform is provided by IQVIA for the purposes of supporting your potential or actual participation in one or more clinical trials or other health-related research (“clinical trials”) and the accompanying use and disclosure of your personal information, either as a patient, caregiver or as a member of the study team (PI, Patient Guide, Study Concierge, etc.). This Privacy Policy covers your full engagement with IQVIA current and future clinical trials and other health care- related research, from your initial interaction with the Platform to the beginning of your contact with a potential trial, through participation in any trial and potential participation in other trials and additional uses of your personal information as identified in this Privacy Policy to support medical research. This Privacy Policy describes how we use, disclose and protect any personal information that we collect or receive from you or on your behalf through this Platform, whether as a potential clinical trial or healthcare research participant, patient, data subject or healthcare professional. If you are participating in a specific clinical trial as a trial participant, this Policy supplements the information you have received or will receive as part of the clinical trial’s informed consent process. The informed consent form (“ICF”) and research protocol will define how information about you will be used in connection with the clinical trial. This Policy is intended to meet applicable legal requirements globally, including in North America, Europe, Asia Pacific and other relevant jurisdictions and supplements the IQVIA Privacy Policy and Online Privacy Policy, which can be found at www.IQVIA.com.

Your Role and Responsibilites

  • You should be familiar with how our Platform works and read all our policies.
  • You should be aware of, and have a right to know, what information is collected on this Platform, how it is stored, protected and used.

Your Rights and Choices

  • You have the right to know the information collection and storage practices of this Platform.
  • You have the right to know how your information will be used and by whom.
  • You have the right to know to whom we may disclose your information, the clinical trial and the ICF.

12. Children’s privacy

This platform, defined to include any access via a web browser and any related application (collectively “Platform”), is provided, owned and managed by IQVIA™. IQVIA is committed to protecting your privacy. This Platform is provided by IQVIA for the purposes of supporting your potential or actual participation in one or more clinical trials or other health-related research (“clinical trials”) and the accompanying use and disclosure of your personal information, either as a patient, caregiver or as a member of the study team (PI, Patient Guide, Study Concierge, etc.). This Privacy Policy covers your full engagement with IQVIA current and future clinical trials and other health care- related research, from your initial interaction with the Platform to the beginning of your contact with a potential trial, through participation in any trial and potential participation in other trials and additional uses of your personal information as identified in this Privacy Policy to support medical research. This Privacy Policy describes how we use, disclose and protect any personal information that we collect or receive from you or on your behalf through this Platform, whether as a potential clinical trial or healthcare research participant, patient, data subject or healthcare professional. If you are participating in a specific clinical trial as a trial participant, this Policy supplements the information you have received or will receive as part of the clinical trial’s informed consent process. The informed consent form (“ICF”) and research protocol will define how information about you will be used in connection with the clinical trial. This Policy is intended to meet applicable legal requirements globally, including in North America, Europe, Asia Pacific and other relevant jurisdictions and supplements the IQVIA Privacy Policy and Online Privacy Policy, which can be found at www.IQVIA.com.

Your Role and Responsibilites

  • You should be familiar with how our Platform works and read all our policies.
  • You should be aware of, and have a right to know, what information is collected on this Platform, how it is stored, protected and used.

Your Rights and Choices

  • You have the right to know the information collection and storage practices of this Platform.
  • You have the right to know how your information will be used and by whom.
  • You have the right to know to whom we may disclose your information, the clinical trial and the ICF.

13. Data retention

This platform, defined to include any access via a web browser and any related application (collectively “Platform”), is provided, owned and managed by IQVIA™. IQVIA is committed to protecting your privacy. This Platform is provided by IQVIA for the purposes of supporting your potential or actual participation in one or more clinical trials or other health-related research (“clinical trials”) and the accompanying use and disclosure of your personal information, either as a patient, caregiver or as a member of the study team (PI, Patient Guide, Study Concierge, etc.). This Privacy Policy covers your full engagement with IQVIA current and future clinical trials and other health care- related research, from your initial interaction with the Platform to the beginning of your contact with a potential trial, through participation in any trial and potential participation in other trials and additional uses of your personal information as identified in this Privacy Policy to support medical research. This Privacy Policy describes how we use, disclose and protect any personal information that we collect or receive from you or on your behalf through this Platform, whether as a potential clinical trial or healthcare research participant, patient, data subject or healthcare professional. If you are participating in a specific clinical trial as a trial participant, this Policy supplements the information you have received or will receive as part of the clinical trial’s informed consent process. The informed consent form (“ICF”) and research protocol will define how information about you will be used in connection with the clinical trial. This Policy is intended to meet applicable legal requirements globally, including in North America, Europe, Asia Pacific and other relevant jurisdictions and supplements the IQVIA Privacy Policy and Online Privacy Policy, which can be found at www.IQVIA.com.

Your Role and Responsibilites

  • You should be familiar with how our Platform works and read all our policies.
  • You should be aware of, and have a right to know, what information is collected on this Platform, how it is stored, protected and used.

Your Rights and Choices

  • You have the right to know the information collection and storage practices of this Platform.
  • You have the right to know how your information will be used and by whom.
  • You have the right to know to whom we may disclose your information, the clinical trial and the ICF.

14. Accountability / Compliance and

This platform, defined to include any access via a web browser and any related application (collectively “Platform”), is provided, owned and managed by IQVIA™. IQVIA is committed to protecting your privacy. This Platform is provided by IQVIA for the purposes of supporting your potential or actual participation in one or more clinical trials or other health-related research (“clinical trials”) and the accompanying use and disclosure of your personal information, either as a patient, caregiver or as a member of the study team (PI, Patient Guide, Study Concierge, etc.). This Privacy Policy covers your full engagement with IQVIA current and future clinical trials and other health care- related research, from your initial interaction with the Platform to the beginning of your contact with a potential trial, through participation in any trial and potential participation in other trials and additional uses of your personal information as identified in this Privacy Policy to support medical research. This Privacy Policy describes how we use, disclose and protect any personal information that we collect or receive from you or on your behalf through this Platform, whether as a potential clinical trial or healthcare research participant, patient, data subject or healthcare professional. If you are participating in a specific clinical trial as a trial participant, this Policy supplements the information you have received or will receive as part of the clinical trial’s informed consent process. The informed consent form (“ICF”) and research protocol will define how information about you will be used in connection with the clinical trial. This Policy is intended to meet applicable legal requirements globally, including in North America, Europe, Asia Pacific and other relevant jurisdictions and supplements the IQVIA Privacy Policy and Online Privacy Policy, which can be found at www.IQVIA.com.

Your Role and Responsibilites

  • You should be familiar with how our Platform works and read all our policies.
  • You should be aware of, and have a right to know, what information is collected on this Platform, how it is stored, protected and used.

Your Rights and Choices

  • You have the right to know the information collection and storage practices of this Platform.
  • You have the right to know how your information will be used and by whom.
  • You have the right to know to whom we may disclose your information, the clinical trial and the ICF.

15. Privacypolicysection15

This platform, defined to include any access via a web browser and any related application (collectively “Platform”), is provided, owned and managed by IQVIA™. IQVIA is committed to protecting your privacy. This Platform is provided by IQVIA for the purposes of supporting your potential or actual participation in one or more clinical trials or other health-related research (“clinical trials”) and the accompanying use and disclosure of your personal information, either as a patient, caregiver or as a member of the study team (PI, Patient Guide, Study Concierge, etc.). This Privacy Policy covers your full engagement with IQVIA current and future clinical trials and other health care- related research, from your initial interaction with the Platform to the beginning of your contact with a potential trial, through participation in any trial and potential participation in other trials and additional uses of your personal information as identified in this Privacy Policy to support medical research. This Privacy Policy describes how we use, disclose and protect any personal information that we collect or receive from you or on your behalf through this Platform, whether as a potential clinical trial or healthcare research participant, patient, data subject or healthcare professional. If you are participating in a specific clinical trial as a trial participant, this Policy supplements the information you have received or will receive as part of the clinical trial’s informed consent process. The informed consent form (“ICF”) and research protocol will define how information about you will be used in connection with the clinical trial. This Policy is intended to meet applicable legal requirements globally, including in North America, Europe, Asia Pacific and other relevant jurisdictions and supplements the IQVIA Privacy Policy and Online Privacy Policy, which can be found at www.IQVIA.com.

Your Role and Responsibilites

  • You should be familiar with how our Platform works and read all our policies.
  • You should be aware of, and have a right to know, what information is collected on this Platform, how it is stored, protected and used.

Your Rights and Choices

  • You have the right to know the information collection and storage practices of this Platform.
  • You have the right to know how your information will be used and by whom.
  • You have the right to know to whom we may disclose your information, the clinical trial and the ICF.

16. Privacypolicysection16

This platform, defined to include any access via a web browser and any related application (collectively “Platform”), is provided, owned and managed by IQVIA™. IQVIA is committed to protecting your privacy. This Platform is provided by IQVIA for the purposes of supporting your potential or actual participation in one or more clinical trials or other health-related research (“clinical trials”) and the accompanying use and disclosure of your personal information, either as a patient, caregiver or as a member of the study team (PI, Patient Guide, Study Concierge, etc.). This Privacy Policy covers your full engagement with IQVIA current and future clinical trials and other health care- related research, from your initial interaction with the Platform to the beginning of your contact with a potential trial, through participation in any trial and potential participation in other trials and additional uses of your personal information as identified in this Privacy Policy to support medical research. This Privacy Policy describes how we use, disclose and protect any personal information that we collect or receive from you or on your behalf through this Platform, whether as a potential clinical trial or healthcare research participant, patient, data subject or healthcare professional. If you are participating in a specific clinical trial as a trial participant, this Policy supplements the information you have received or will receive as part of the clinical trial’s informed consent process. The informed consent form (“ICF”) and research protocol will define how information about you will be used in connection with the clinical trial. This Policy is intended to meet applicable legal requirements globally, including in North America, Europe, Asia Pacific and other relevant jurisdictions and supplements the IQVIA Privacy Policy and Online Privacy Policy, which can be found at www.IQVIA.com.

Your Role and Responsibilites

  • You should be familiar with how our Platform works and read all our policies.
  • You should be aware of, and have a right to know, what information is collected on this Platform, how it is stored, protected and used.

Your Rights and Choices

  • You have the right to know the information collection and storage practices of this Platform.
  • You have the right to know how your information will be used and by whom.
  • You have the right to know to whom we may disclose your information, the clinical trial and the ICF.

17. Privacypolicysection17

This platform, defined to include any access via a web browser and any related application (collectively “Platform”), is provided, owned and managed by IQVIA™. IQVIA is committed to protecting your privacy. This Platform is provided by IQVIA for the purposes of supporting your potential or actual participation in one or more clinical trials or other health-related research (“clinical trials”) and the accompanying use and disclosure of your personal information, either as a patient, caregiver or as a member of the study team (PI, Patient Guide, Study Concierge, etc.). This Privacy Policy covers your full engagement with IQVIA current and future clinical trials and other health care- related research, from your initial interaction with the Platform to the beginning of your contact with a potential trial, through participation in any trial and potential participation in other trials and additional uses of your personal information as identified in this Privacy Policy to support medical research. This Privacy Policy describes how we use, disclose and protect any personal information that we collect or receive from you or on your behalf through this Platform, whether as a potential clinical trial or healthcare research participant, patient, data subject or healthcare professional. If you are participating in a specific clinical trial as a trial participant, this Policy supplements the information you have received or will receive as part of the clinical trial’s informed consent process. The informed consent form (“ICF”) and research protocol will define how information about you will be used in connection with the clinical trial. This Policy is intended to meet applicable legal requirements globally, including in North America, Europe, Asia Pacific and other relevant jurisdictions and supplements the IQVIA Privacy Policy and Online Privacy Policy, which can be found at www.IQVIA.com.

Your Role and Responsibilites

  • You should be familiar with how our Platform works and read all our policies.
  • You should be aware of, and have a right to know, what information is collected on this Platform, how it is stored, protected and used.

Your Rights and Choices

  • You have the right to know the information collection and storage practices of this Platform.
  • You have the right to know how your information will be used and by whom.
  • You have the right to know to whom we may disclose your information, the clinical trial and the ICF.

18. Privacypolicysection18

This platform, defined to include any access via a web browser and any related application (collectively “Platform”), is provided, owned and managed by IQVIA™. IQVIA is committed to protecting your privacy. This Platform is provided by IQVIA for the purposes of supporting your potential or actual participation in one or more clinical trials or other health-related research (“clinical trials”) and the accompanying use and disclosure of your personal information, either as a patient, caregiver or as a member of the study team (PI, Patient Guide, Study Concierge, etc.). This Privacy Policy covers your full engagement with IQVIA current and future clinical trials and other health care- related research, from your initial interaction with the Platform to the beginning of your contact with a potential trial, through participation in any trial and potential participation in other trials and additional uses of your personal information as identified in this Privacy Policy to support medical research. This Privacy Policy describes how we use, disclose and protect any personal information that we collect or receive from you or on your behalf through this Platform, whether as a potential clinical trial or healthcare research participant, patient, data subject or healthcare professional. If you are participating in a specific clinical trial as a trial participant, this Policy supplements the information you have received or will receive as part of the clinical trial’s informed consent process. The informed consent form (“ICF”) and research protocol will define how information about you will be used in connection with the clinical trial. This Policy is intended to meet applicable legal requirements globally, including in North America, Europe, Asia Pacific and other relevant jurisdictions and supplements the IQVIA Privacy Policy and Online Privacy Policy, which can be found at www.IQVIA.com.

Your Role and Responsibilites

  • You should be familiar with how our Platform works and read all our policies.
  • You should be aware of, and have a right to know, what information is collected on this Platform, how it is stored, protected and used.

Your Rights and Choices

  • You have the right to know the information collection and storage practices of this Platform.
  • You have the right to know how your information will be used and by whom.
  • You have the right to know to whom we may disclose your information, the clinical trial and the ICF.

19. Privacypolicysection19

This platform, defined to include any access via a web browser and any related application (collectively “Platform”), is provided, owned and managed by IQVIA™. IQVIA is committed to protecting your privacy. This Platform is provided by IQVIA for the purposes of supporting your potential or actual participation in one or more clinical trials or other health-related research (“clinical trials”) and the accompanying use and disclosure of your personal information, either as a patient, caregiver or as a member of the study team (PI, Patient Guide, Study Concierge, etc.). This Privacy Policy covers your full engagement with IQVIA current and future clinical trials and other health care- related research, from your initial interaction with the Platform to the beginning of your contact with a potential trial, through participation in any trial and potential participation in other trials and additional uses of your personal information as identified in this Privacy Policy to support medical research. This Privacy Policy describes how we use, disclose and protect any personal information that we collect or receive from you or on your behalf through this Platform, whether as a potential clinical trial or healthcare research participant, patient, data subject or healthcare professional. If you are participating in a specific clinical trial as a trial participant, this Policy supplements the information you have received or will receive as part of the clinical trial’s informed consent process. The informed consent form (“ICF”) and research protocol will define how information about you will be used in connection with the clinical trial. This Policy is intended to meet applicable legal requirements globally, including in North America, Europe, Asia Pacific and other relevant jurisdictions and supplements the IQVIA Privacy Policy and Online Privacy Policy, which can be found at www.IQVIA.com.

Your Role and Responsibilites

  • You should be familiar with how our Platform works and read all our policies.
  • You should be aware of, and have a right to know, what information is collected on this Platform, how it is stored, protected and used.

Your Rights and Choices

  • You have the right to know the information collection and storage practices of this Platform.
  • You have the right to know how your information will be used and by whom.
  • You have the right to know to whom we may disclose your information, the clinical trial and the ICF.

20. Privacypolicysection20

This platform, defined to include any access via a web browser and any related application (collectively “Platform”), is provided, owned and managed by IQVIA™. IQVIA is committed to protecting your privacy. This Platform is provided by IQVIA for the purposes of supporting your potential or actual participation in one or more clinical trials or other health-related research (“clinical trials”) and the accompanying use and disclosure of your personal information, either as a patient, caregiver or as a member of the study team (PI, Patient Guide, Study Concierge, etc.). This Privacy Policy covers your full engagement with IQVIA current and future clinical trials and other health care- related research, from your initial interaction with the Platform to the beginning of your contact with a potential trial, through participation in any trial and potential participation in other trials and additional uses of your personal information as identified in this Privacy Policy to support medical research. This Privacy Policy describes how we use, disclose and protect any personal information that we collect or receive from you or on your behalf through this Platform, whether as a potential clinical trial or healthcare research participant, patient, data subject or healthcare professional. If you are participating in a specific clinical trial as a trial participant, this Policy supplements the information you have received or will receive as part of the clinical trial’s informed consent process. The informed consent form (“ICF”) and research protocol will define how information about you will be used in connection with the clinical trial. This Policy is intended to meet applicable legal requirements globally, including in North America, Europe, Asia Pacific and other relevant jurisdictions and supplements the IQVIA Privacy Policy and Online Privacy Policy, which can be found at www.IQVIA.com.

Your Role and Responsibilites

  • You should be familiar with how our Platform works and read all our policies.
  • You should be aware of, and have a right to know, what information is collected on this Platform, how it is stored, protected and used.

Your Rights and Choices

  • You have the right to know the information collection and storage practices of this Platform.
  • You have the right to know how your information will be used and by whom.
  • You have the right to know to whom we may disclose your information, the clinical trial and the ICF.