Enhance your Clinical Trial Document process in order to ensure a complete TMF, remain inspection ready, improve clinical quality and new technologies.
WHY CLINICAL DOCUMENT WORLD SHOULD BE YOUR LEARNING & NETWORKING CHOICE OF THE YEAR
45+ Educational sessions cover all aspects of clinical document management including regulatory guidance, compliance, quality, technology.
Hear from 50+ leaders with a background in clinical operations, TMF, quality, technology, and inspections.
Focus on developing a strategic TMF management plan that increases quality and ensures TMF completeness.
Develop and maintain a culture of inspection readiness.
Impact of site – Sponsor – CRO collaboration to improve quality
Discover new technologies that can assist in document management as well as how to implement and roll them out seamlessly.
Price:
General Admission: USD 295.0
Time: 9:00 am - 5:00 pm
Sign up and follow your favorite conferences.