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Tuesday, November 2, 2010

DCGI becoming more and more vigilent and making the laws stringent in Pharma

it is well known by every personnel in pharma sector the recent updates of implementation of Certification of all the pharma bodies acording to Schedule-M and certifications w.r.t WHO are not beiong provided for every industry but basing in the requirement only these are being audited which was a daily process earlier to the recent implementation from 01 Nov. 2010 as mandatory for Schedule L (For GLP)leaving behind the industry plea to extend the timeline as it is 2 years from its release and again it is now concentrating on the formulation of Good distribution practices which might also become a mandatory guideline in future.

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