Use of Booklet Labels on Investigational Medicinal Products (IMPs) | ISPE | International Society for Pharmaceutical Engineering
Challenges in Paediatric Clinical Trials: How to Make It Feasible | IntechOpen
EU-Clinical Trials Register - Sindbad
What Is Clinical Trial Process Flow As Per FDA? - Pharmabeej
Investigational Medicinal Product (IMP) | Noclor
From IMPD to IND – same but different - Biopharma Excellence
IMP-Track
When innovation outpaces regulations: The legal challenges for direct‐to‐patient supply of investigational medicinal products - Malone - 2022 - British Journal of Clinical Pharmacology - Wiley Online Library
and use of Auxiliary Medicinal Products (AMPs)
Phase 1 clinical trial
Investigational Medicinal Product (IMP) Management - ScienceDirect
Phase I and first-in-human Clinical Trials and FDA's CGMP Requirements
Effective delivery of Complex Innovative Design (CID) cancer trials—A consensus statement | British Journal of Cancer
CTTI Recommendations: Decentralized Clinical Trials
Understanding the new EU Clinical Trial Regulation
Clinical Trials Research Governance | UNSW Research
Good Distribution Practice For Clinical Trial Materials | IVT
Investigational Medicinal Products— Optimizing the Supply Chain
The EU Qualified Person (QP) Demystified Fool-Proofing Your EU Phase 1 Trial
A New Approach to Temperature Monitoring in a Changing Clinical Supply Chain Environment
ADVANCED CLINICAL TRIALS Introduction to clinical research - ADVANCED CLINICAL TRIALS
What is a clinical trial? | risklick company
Section D - IMP Identification
Good Distribution Practice For Clinical Trial Materials | IVT
