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PHARMACOKINETIC TOXICOLOGY SITE  MANAGEMENT REGULATORY AFFAIRS BIOMETRICS MEDICAL WRITING THERAPEUTIC

    Clinical Studies
   
      SCOPE OF ACTIVITY
         
        The studies are undertaken with competent Principle Investigators at the desired institutes in India at all major centres. The Clinical studies of Phase II/III/IV and promotional nature studies are undertaken in a GCP compliant manner. We also undertake the drug experience report on various products
           
          1. Protocol design with biometric support

2. IRB/EC documentation

3. Regulatory submissions

4. CT registration to national authorities

5. Conduct of the study

6. Compilation of CRF

7. Analysis of results and conclusion

8. Final report writing
 
     
    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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