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standard operating procedure are the important document for pharmaceutical company & organizatio...
In this Analysis, well look at how QbD is being practised right now. QbD represents a cutting edge m...
31/03/2015 Hard gelatin capsule shells are used as soluble containers for incorporation of drugs or...
Pharmaceutical regulatory affair is the interface between pharmaceutical industry and the regulatory...
ICH guidelines covering Q- Quality guidelines. it include develop to evolution of ICH.
WHO Good Manufacturing Practice Requirements Good Manufacturing Practice is the part of quality ass...
Pharmaceutical Quality affects every individual. Therefore GMP is required to ensure the quality of ...
It's all about the topic of documentation in pharmaceutical industry. In this the specifications...
A Study on Documentation Maintenance in the Pharmaceutical Industry which includes the main records ...
GxP is a general abbreviation for the "good practice" quality guidelines and regulations. ...
Good Manufacturing Practice is a set of regulations, codes, and guidelines for the manufacture of d...
Documentation in technology transfer covers technology transfer plan, technology transfer report,pro...
The presentation is about documentation in the pharmaceutical industry. Many important topics are co...
COMPLAINT HANDLING IN PHARMACEUTICAL COMPANIES,�PRODUCT RECALL,RETENTION RECORDS, DISTRIBUTION RE...
REGULATORY AND INDUSTRY VIEWS ON QbD
To define specifications and procedures for all materials and method of manufactured and control. T...
DOCUMENTATION IN PHARMACEUTICAL INDUSTRY : WORKING INSTRUCTIONS AND RECORD FORMATS To define specifi...
Prepared BY- Ruhid Hasan from:- University of Development Alternative dept. of Pharmacy [Life Scince...
What is Lean Authoring? Why Lean Authoring? Advantages of Lean Authoring How to apply Lean Authoring...
ICH GUIDELINE .M.PHARM , B.PHARM REGULATORY AFFAIRS
Indian GMP Certification & WHO GMP Certification by Mr. Vishal Shelke https://youtube.com/visha...
ICH Guidelines were created by The International Council for Harmonization of Technical Requirements...
Use of QA and QC in Pharmaceutical Industries
DOCUMENTATION IN PHARMACEUTICAL INDUSTRY, BY Dr. UMESH KUMAR SHARMA
