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Guidelines to GLP
validation types
ich guidelines for clinical trials, general principles, scientific approach .
Good Laboratory Practices, Protocol, Contents of protocol, Conduct of a non-clinical laboratory stud...
Good Clinical Practices and Investigator responsibilities
21 CFR 312 and 314 are two separate, but related, US Food and Drug Administration (FDA) regulations ...
IND enabling
GLP in drug discovery and development process and how to practice GLP.
A Data Management Plan (DMP) describes data that will be acquired or produced during research; how t...
A standard for the design, conduct, performance, monitoring, auditing, recording, analyses and repor...
Crp
Schedule y
This document describes the detailed information of clinical trial protocol and protocol design. The...
What is a clinical trial protocol? Clinical research is conducted according to a plan (a protocol) o...
BBAU LUCKNOW
schedule y of drugs and cosmetic acts
Protocols for Clinical Research
Requirements And Guidelines For Permission To Import / or Manufacture of New Drugs For Sale or To Un...
Clinical Research and Pharmacovigilance
Roles and Responsibilities in Clinical Trials of Investigator, Study Coordinator, Sponsor, Monitor, ...
there are many clinical trials every day but good reporting of these trials is essential. This talk ...
Turacoz Skill Development Program provides medical writing training on various types of regulatory d...
USFDA process validation
Guidlines given for GLP
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