Pitfalls to Avoid in Clinical Data Collection and Management
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Clinical data collection and management are critical components of clinical research, forming the backbone of any clinical trial. Ensuring…
The Evolving Role of Clinical Data Managers in Patient-Centric Clinical Trials
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The shift towards patient-centric clinical trials represents a significant evolution in the landscape of clinical research, placing patients at the…
Boosting Trial Efficiency and Accuracy by Integrating Biostatistics & Data Management
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Integrating statistics and data management within a single team during clinical trials can significantly boost efficiency, accuracy, and reliability…
Lunch and Learn: Navigating FDA’s Expectations for Drug Approval
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IDDI is pleased to invite you to an exceptional Lunch and Learn on dose optimization, accelerated approval and adaptive designs:…
IDDI Lunch & Learn in Durham, NC
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SAILING SMOOTH SEAS: CHARTING THE COURSE THROUGH NEEDED ADVANCEMENTS IN SAFETY REPORTING AND NEW FDA GUIDANCE ON IDMCs IDDI and…
Lunch & Learn in South San Francisco, CA
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REGULATORY AND DESIGN TRENDS IN CLINICAL TRIALS IDDI and OWL Oncology Research are pleased to invite you to an exceptional…
Why do so many phase 3 trials fail?
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Randomized controlled trials (RCTs), particularly in phase 3, are the preferred sources of evidence for drug approval and reimbursement…
Best Practices to Accelerate Your Database Lock
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Accelerating database lock in clinical research is a critical aspect of ensuring timely study conclusions and decision-making. Database lock…
The Key to Successful Regulatory Submission: Ensuring 100% SDTM Compliance in Your SAS Database
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In the complex and highly regulated world of clinical trials, the submission of data to regulatory authorities is a critical…
Accelerated approvals (AA): not so fast!
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Everardo D. Saad, MD, Medical Director and Consultant, IDDI Marc Buyse, ScD, Chief Scientific Officer and Consultant, IDDI The development…