Products
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Subject Recruitment: Proactive Project Plans and Issues Management -
Technology Innovation and Intellectual Property (IP) in the Biomedical Industry -
The Clinical Research Finance Roadmap Companion Reference Guide: Tools, Templates and Resources (Electronic) -
The Clinical Research Finance Roadmap: A Comprehensive Guide to the Financial Aspects of Clinical Research -
The CRA Role in Risk-Based Monitoring: Strategies for Effective Remote Monitoring -
The Form FDA 1572: A Reference Guide for Clinical Researchers, Sponsors, and Monitors -
The Fundamentals of Clinical Research Project Management -
The GCPs of Essential Documents -
The IND in a CTD/eCTD Format -
Training Portal Subscription -
Trial Master File (TMF) for Sponsors: Set Up and Maintenance -
Understanding ICH E6(R3) (GCP) Updates: Key Changes from R2 -
Understanding ICH E6(R3) (GCP) Updates: Key Changes from R2 -
Use of Notes to File in Clinical Trial Essential Documentation -
Use of Notes to File in Clinical Trial Essential Documentation -
Utilization of Real-World Evidence (RWE) and Real-World Data (RWD) and Regulations -
Working with Clinical Research Sites: Strategic Planning and Operations for Sponsors and CROs -
WORKSHOP: Trial Master Files: Why They Are Important and How to Organize Them -
Writing and Updating the Investigator's Brochure -
Writing Pharmacology Sections of an IND Application -
Writing Pharmacology Sections of an IND Application -
Writing the Clinical Study Protocol -
Writing the Clinical Study Report -
Writing Toxicology Sections of an IND Application
