ICH guidance on the Structure and content of clinical study reports; aims to allow the compilation of a single core clinical study report acceptable to all regulatory authorities of the ICH regions.
Source: EMA
Glossary
ICH E3
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Take advantage of the knowledge and best practices gained from more than 20 years of research, innovation and development for the health and life sciences sectors.
Glossary
The Life Sciences glossary with terminology, acronyms, for regulatory, quality, compliance, clinical trials, and pharmacovigilance software.
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