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GMP in Pharma industry
SUPAC Guidelines for MR tablets by FDA
CHF latest guidelines. Recent advances in drug treatment of CHF included. Recent FDA approved drugs ...
Pharmacovigilance is the science and activities related to the detection, assessment, understanding,...
This comprehensive guide provides a detailed exploration of the ANDA (Abbreviated New Drug Applicati...
Medical devices keep evolving, and with cutting edge technologies such as AI and Cloud, they are con...
Thinking of starting your own line of supplements? But are you aware of the regulations you have to ...
The pharmaceutical Quantity by Design (QbD) is a systemic approach to development that begins with p...
the manufacture of drugs through the lens of pharmaceutical jurisprudence. This presentation provide...
This document presents a summary of the cGMP and industrial management by Miss Priyanka Sharma. In 1...
CGMP (Current Good Manufacturing Practice) refers to a set of regulations and guidelines enforced by...
Validation is the backbone of pharmaceutical quality assurance. This deck covers equipment qualifica...
Regulatory aspects of clinical trials refer to the rules, regulations, and guidelines set forth by r...
This presentation provides a comprehensive overview of TGA (Therapeutic Goods Administration) regula...
This presentation gives a complete brief idea of how FDA regulates the marketing of Generic drugs. A...
This presentation covers the ICH guidelines coding no in details.
Various countries around the world have distinct drug regulatory bodies tasked with overseeing the s...
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Pharmaceutical Regulataory Affairs
Essential Safety Requirements (ESR) in healthcare refer to a set of criteria and standards that medi...
Food Nutrition
Describing the Industry's/sponsor's/drug manufacturers' perspective of the Investigation...
Project work ppt
Quality & compliance excellence in pharmaceuticals
