Your search for Principles of Global Clinical Research for Medical Devices returned the following most recent results.

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Regulatory Science Virtual Symposium: “Principles of Global Clinical Research for Medical Devices” Session 2: Clinical Investigation: Principles from Harmonized Documents (2021)

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Regulatory Science Virtual Symposium: “Principles of Global Clinical Research for Medical Devices” Session 5: Developing Clinical Evaluations (2021)

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Regulatory Science Virtual Symposium: “Principles of Global Clinical Research for Medical Devices” Session 1: Introduction (2021)

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Regulatory Science Virtual Symposium: “Principles of Global Clinical Research for Medical Devices” Session 4: From Clinical Data to Clinical Evidence (2021)

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Regulatory Science Virtual Symposium: “Principles of Global Clinical Research for Medical Devices” Session 6: Wrap-Up (2021)

regulatory & quality sciences

Regulatory Science Virtual Symposium: “Principles of Global Clinical Research for Medical Devices” Session 3: Good Clinical Practices and ISO 14155 (2021)

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Regulatory Science Boot Camp Lecturers Discuss Processes and Requirements in Patient-Centered Drug Development

Regulatory Science Boot Camp Lecturers Discuss Processes and Requirements in Patient-Centered Drug Development

The patients who actually take medications and live with their conditions are uniquely qualified to contribute to the drug development process. An evolving body of research regulations and approaches seek to ensure that patients' perspectives are incorporated into studies in a meaningful manner.

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