Answer: set standards for the design conduct monitoring and reporting of clinical research
Most relevant text from all around the web:
ICH GCP guidelines do what?
Difference Between Indian GCP & ICH-GCP
Genelife Clinical Research Pvt. Ltd.: Difference Between Indian GCP & IC…
ICH Guidelines
Guidelines : ICH
Are you ready for the ICH GCP E6 (R2) Addendum? - TCTC Group
Good Documentation Practices - GMPTraining.com
This International Conference on Harmonization ( ICH ) document makes recommendations on information that should be included in a core clinical study report of an individual study …
ICHGCP .NET will help you to make the best choice. Our website is updated daily! " ICHGCP .NET Team" can offer you hundreds of clinical research jobs
Good Clinical Practice (GCP) is an international ethical and scientific quality standard for designing conducting recording and reporting trials that involve the participation of human subjects.
Fri Jun 08 2018 · FDA Guidance for Good Clinical Practice ( GCP ) is an international quality standard defined by the International Council for Harmonization ( ICH ) that governs ethical and scientific considerations for designing conducting recording and reporting trials involving hu...
Disclaimer:
Our tool is still learning and trying its best to find the correct answer to your question. Now its your turn, "The more we share The more we have". Comment any other details to improve the description, we will update answer while you visit us next time...Kindly check our comments section, Sometimes our tool may wrong but not our users.
Are We Wrong To Think We're Right? Then Give Right Answer Below As Comment
No comments:
Post a Comment