Pharmaceutical validation is important to the manufacturing process to ensure product consistency and safety. It involves the regulation of all raw materials and production procedures as well as testing of the final product. The general rule of thumb is to follow good manufacturing practices (GMP). This demands that all protocols be up to date and followed by trained personnel. It also requires that equipment be well-maintained and inspected. In the case of clean-room usage, the cleanroom needs to be verified.
The International Council for Harmonization of Technical Requirements for Pharmaceuticals for Human Use (ICH) was founded in 1990 by the regulatory bodies of Japan (MHLW), the European Union (EMA), and the United States (FDA). This international effort has standardized the protocols for pharmaceutical validation so that drugs developed, manufactured, approved, and registered in one member country can be fast-tracked to approval and distribution in another member country. The guidelines address rigorous testing protocols for new drug molecules including stress testing, packaging systems, storage conditions, labeling, and shelf life. These guidelines speed up the drug development process and get life-saving drugs to consumers quickly and safely.

Face book-
[ Ссылка ]

Instagram -[ Ссылка ]

Twitter -[ Ссылка ]

Linkedin (Karan Ajay Gupta)-karangupta0411@gmail.com

Address for those people and students who are interested in training and consultancy service-
B.R. NAHATA COLLEGE OF PHARMACY, NEAR KRISHI UPAJ MANDI, MHOW- NEEMUCH ROAD, MANDSAUR (M.P.) 458001

EMAIL ID-
(1) DIRECTOR.BRNCOP@MEU.EDU.IN
(2) KARAN.GUPTA@MEU.EDU.IN

Disclaimer - video is for educational purposes only. Copyright Disclaimer Under Section 107 of the Copyright Act 1976, allowance is made for "fair use" for purposes such as criticism, comment, news reporting, teaching, scholarship, and research. Fair use is a use permitted by copyright statute that might otherwise be infringing. Non-profit, educational, or personal use tips the balance in favor of fair use.

THANKS FOR WATCHING.
#VALIDATION #PRINCIPLE #WHATIS #KARANAJAYGUPTA #M.PHARMACY #BPHARMACY #PHARMACEUTICALINDUSTRY #GMP #CGMP #GLP#HINDI #KARANAJAYGUPTA #APPLICATION #IMPORTANCE #QUALITYCONTROL #QC #QA #PHARMACEUTICALINDUSTRY #JOB #NAUKRI #SKILLDEVELOPMENT

свернуть