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CLINICAL TRIALS PHARMACOKINETIC TOXICOLOGY SITE  MANAGEMENT BIOMETRICS MEDICAL WRITING THERAPEUTIC

    Regulatory Affairs
   
      SCOPE OF ACTIVITY
         
        The regulatory affairs matters include providing information about the requisite documentations, procedures involved, payment of regulatory fees, rechecking the provided documents and final submission to the regulatory directorate. Follow up, collection of documents till final outcome.
           
         

1. Registration of Products in India

2. Documentation/ CTD/ eCTD Dossier preparation

3. PSUR

4. Advisory functions

 
     
    International Strategic Partners
           
      U.K.
Dr. NAEEM KHAN
Consultant Pharmaceuticals and Allied Industries,

U.S.A
Mr. JURIJ PETRIN,
MD President and CEO
Pharmaceutical Regulatory Services, Inc.
 
   
 
     
     
       
 
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    Director’s Blog  
    Discussion Of Past Events, Current Issues And What The Future May Look Like In The Healthcare Industry And Medical Education  
       
   
 
     
       
 
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