Found 445 presentations matching your search
New drug development stages.
Master formula record, DMF (Drug Master File), Distribution records. Generic drugs product developme...
GCP course material
renewable energy
Safety data generation Pre clinical phase Clinical phase Post approval phase (PMS)
- Whilst the realization of the CTD took many years, there is now a common format for the submission...
The main principle involved in the FBP is the air suspension in which the material to be coated is s...
Started to create milestones, we, C- Tech Engineers Private Limited marked our presence in the year ...
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Unit-III, Chapter 1. Registration of Indian Products in Overseas Market. B. Pharm. Final Year, Sem-V...
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Software development is evolving rapidly, driven by advancements in AI, cloud computing, and automat...
Indian regulatory requirements- CDSCO
regulatory affairs
Phase 0 and Phase 1 Clinical Trial
Solutions like the ELK Stack are vital for aggregating, processing, storing, and analyzing logs, en...
Earthworms account for their highest biomass among tropical soil macro-fauna and also called “Ecos...
It is applicable for the Generic drugs
That slides would help students to know about clinical trials, safety of patient/healthy subjects an...
DMF of Japan and Drug Regulatory Approval procedure
this is a presentation about randomized clinical trials, in which it describes the phases of clinica...
The Common Technical Document (CTD) is a standardized format for regulatory submission of informatio...
includes the details of new drug development and different phases of clinical trials
