Corporate Resources

Corporate Resources

- Articles
Addressing eCTDs
Addressing the Unique Needs of Emerging Biopharma in Drug Development
CEO Steve Powell Named to PharmaVOICE 100’s Most Inspiring People in Life Sciences
GDPR & Data Protection: Key Changes Drug Developers Need to Know About
Interview: Surviving the Paperwork After Clinical Stage Drug Development
New Regulatory Standards for Pharmaceutical Advertising and Promotional Materials
The Science of Site Selection
- Brochures
Corporate Overview
- Case Studies
Asthma Trial
Evidence-Driven Feasibility Speeds Start-up for Global, Phase III, Gene Therapy Trials for Neuromuscular Disorder
IND Submission and Acceptance by the FDA of a Combination Product
Phase II Trial in Ulcerative Colitis Patients
Synteract Exceeds Biopharmaceutical Company’s Expectations With Our Functional Service Provider (FSP) Model
Synteract Exceeds Enrollment Expectations in Complex Parallel Studies While Sharing Monitoring Services (Kidney Disease)
Synteract Helps Complete Two Sequential, Critical Double-Masked Phase III Ophthalmology Studies
- Checklists
4 Ways to Know Adaptive Trial Design Is Right For Your Trial
- Data Sheets
eCTD
Functional Support Services
Ready Set Submit
Regulatory Affairs
- Guides
Is Your Study In Need of a Rescue?
Safety Services: A Critical Component of Clinical Trials
- Presentations
Achieving a Key Milestone: Site Activation
Preparing for FDA Mandated eCTD Submissions
- Videos
Why Synteract?
- Webinars
Achieving Orphan Drug Designation: A Global Regulatory Perspective
Achieving Scalability and Reducing Costs with an FSP Model
Addressing the Rapidly Evolving Vaccine Development Landscape
Business Continuity in Drug Development Due to the COVID-19 Pandemic
Integrated Summaries: Planning for the Unexpected & Reacting to the Unforeseen
Optimizing Clinical Trials Using Adaptive Design: Early Alignment for Success
The Increasing Role of Pharmacometrics in Drug Development
Utilizing Inventive Biostatistical Methods to Enhance Rare Disease Trials
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