Pharma Treasures

Pharma treasures is an informatory site, which shares pharma related articles. The ultimate goal of this site is to become a knowledge hub by gathering all pharma related technical information under one roof...... This blog mainly talks about QMS,cGMP,Regulatory Filings & Guidelines,Validation & Qualifications,Drug Stability,FDA 483s &Media Fill. Hope this blog will cater the needs of both fresher’s and experienced professionals.

Wednesday, 4 December 2019

21 CFR Part 211 – Current Good Manufacturing Practice for Finished Pharmaceuticals

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21 CFR Part 211 – Current Good Manufacturing Practice for Finished Pharmaceuticals FDA ensures the quality of dru...
1 comment:
Saturday, 30 November 2019

Pre-Launch Activities Importation Requests (PLAIR)

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Pre-Launch Activities Importation Requests (PLAIR) USFDA’s PLAIR program allows the foreign drug product manufac...
20 comments:

Role of U.S. Agent for Importing Food, Drug and Medical Devices in US Market

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Role of U.S. Agent for Importing Food, Drug and Medical Devices in US Market When registering with USFDA for...
1 comment:
Monday, 18 November 2019

Role of an RLD in an ANDA

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Role of an RLD in an ANDA A Reference Listed Drug (RLD) is an approved drug product to which the ANDA applicant ...
Wednesday, 25 September 2019

Pharmaceutical products - Stability study & Mass balance concerns

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Pharmaceutical products - Stability study & Mass balance concerns Mass Balance concept   Ass...
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About Pharmatreasures

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Pharmatreasures is an online platform dedicated to healthcare professionals including medical devices, pharmaceuticals and biologics. Join our facebook group! Stay informed on the latest healthcare regulatory news and guideline updates. https://www.facebook.com/groups/754923708611548/ We strive to make industrial content (updates in regulations, guidance, enforcement actions, business updates and lot more….) available to you on daily basis in the manner that is most convenient for you. Keeps you informed about the changing regulatory landscape through regular updates, in-depth articles and analysis. Providing a forum to discuss industry related practices and requirements…….where people can post questions and answers.
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