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Evaluation
How to design & conductpre-clinical trials?
Pre-clinical trials aim to generate crucial data on thesafety, functionality, and biocompatibility of a medicaldevice, providing foundational evidence for regulatorysubmission and clinical trial approval
Discover our full repository
Clinical Investigations Guidance
MHRA
Guide
Free
FDA/ISO
Use of International StandardISO 10993-1, Biologicalevaluation of medical devices
Guideline
Biocompatibility Standards -ISO 10993-1:2018
ISO
Standard
Not Free
Clinical Trials Routemap
NIHCR
Tutorial/Guide
Good Clinical Practice (GCP)
European Medicines Agency
Animals (Scientific Procedures)Act 1986 - consolidated version
UK Government Legislation