Also known as: imp.
IMP stands for various terms. Discover the full forms, meanings, and possible interpretations of IMP across different fields and industries.
The Investigational Materials Plan (IMP) is a critical document in the field of medicine, outlining the strategy for the use of investigational materials in clinical trials. It ensures that all materials are used safely and effectively, adhering to regulatory standards. The plan details the handling, storage, and distribution of these materials, minimizing risks to participants and ensuring the integrity of trial data.
In the context of clinical research, the IMP serves as a blueprint for managing investigational products, from their procurement to their disposal. It includes protocols for quality control, documentation, and compliance with ethical guidelines. This comprehensive approach supports the advancement of medical knowledge while safeguarding patient welfare and maintaining public trust in clinical research.
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