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February 28, 2020

Predicting the Unpredictable: What’s Missing from your Vendor Review?
February 27, 2020

Part 1: Rare Disease Clinical Research – Spotlight on the Patient and Caregiver
February 26, 2020

Cell and Gene Therapy: Taking a New Facility from Construction to Production
February 26, 2020

EDC vs eSource: Is it Time to Move?
February 26, 2020

Clinical Trial Innovations – How Digital Technology is Transforming Clinical Labelling
February 25, 2020

Applying Data Analytics and a Decentralized Trial Platform for More Efficient Patient-Centric Trials
February 20, 2020

Improving Patient Adherence and Outcome Measurement with Game Design
February 20, 2020

EU MDR: Best Practices for UDI Data & Product Labeling
February 18, 2020

Applications of Immunosequencing in Autoimmunity
February 13, 2020

Globalization of Risk Management: Think Globally, Act Locally
February 13, 2020

The Optimal Clinical Data Delivery Infrastructure to Facilitate Data Access & Review
February 12, 2020

Surviving and Thriving in Due Diligence – Major Transactions from the Perspective of Small Pharma
February 06, 2020

Risk Management Plans: GVP Module V Revision 2 and Its Local Impact in the EU
January 30, 2020

Sponsor Oversight Responsibilities for IRT: Proactive Management that Meets Regulatory Scrutiny
January 29, 2020

Moving From Documents to Data: Improving Management and Traceability of Critical Data in Medical Device Manufacturing
January 29, 2020

Age-Appropriate Formulation Development for Pediatric Trials: Challenges and Considerations