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Moving Toward the Implementation Deadline — Approaching MDR Compliance
Industry reports indicate many companies still seem unprepared as they struggle to understand MDR compliance. Learn more about how to comply.
Estimands in Oncology Trials
PPD’s cross-functional estimands working group explores how the ICH E9 addendum impacts oncology clinical trials.
The Value of Patient Experience Data
Qualitative interviews can generate meaningful patient data to inform trial design and gain deeper understanding of treatment experience.
European Union Clinical Trials Regulation: Clinical Trials Information System
PPD experts explain the key features of the Clinical Trials Information System (CTIS), which has been introduced alongside the new EU CTR.
The Present and Future of Conditional Regulatory Authorization and Access Pathways for ATMPs
Advanced Therapy Medicinal Products (ATMPs) are some of the most technologically innovative treatments today. Explore the authorization and access landscape.
FSP Quality Assurance
PPD FSP quality assurance solutions help biotech, biopharmaceutical and medical device companies to ensure the safety and integrity of clinical trials.
Virtual Support Improves Patient, Site and Sponsor Experiences in Clinical Trials
Learn how virtual support can help address challenges that patients and sites may face in clinical trials.