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28th Feb 2012: Sanhar is leveraged with Regional specific Regulatory Submission expertise and be able to help the customers in Multi Geographical Regulatory Submissions.

20th Feb 2012: Sanhar is an Associate Member of Indian Drug Manufacturers Association (IDMA), enabled with a gateway to reach out to more Domestic Customers now.

06th Jan 2012: Sanhar Joins hands with “Registrar Corp”, an U.S. based company to leverage its Regulatory Consulting services pertaining to the U.S. FDA Registration related Businesses.

 
 
 
 
Developing the Validation Rationale for various specific circumstances in alignment with Risk Based GxP Computer System Validation approach
 
Software Quality Assurance is a broader term to address multiple compliance related activities within an organization such as Managing Compliance,
SANHAR’s Regulatory Affairs Consulting team is up to date with current Regulatory requirements, Interpretation of Global Regulations,
 
Paper based regulatory submissions are becoming obsolete and e-submissions are the upcoming trend. The eCTD submissions
Audit is a fact finding process which helps any organization to get aligned to the journey towards continual improvement. It is mandated
 
Personnel Qualification with appropriate Training to perform and supervise any specific activity/function is mandated as per the regulations.
 
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