Clinical Data Management-ClinVigilant

 Clinvigilant supports biotech, pharmaceutical and medical device companies with tailored clinical Operation Services. We combine the full-service capabilities and global reach of a large CRO with the flexibility and personal approach only a mid-size CRO can deliver. With Clinvigilant you get a shared commitment to your success.

 Expect more. At ClinVigilant we are pleased to support you on your path to achieving your goals and to finding solutions together with success, thus we offer you the following services: eClinical Solution Manage end to end clinical trial process from Patient Registration to Sample Management for

 1. Phase I / BA/BE Clinical Trials

 2. Phase II- IV Clinical Trials

 3. PMS / Registry Clinical Trials Clinical Trial Operation 

     1. End to End Clinical Trial Operation 

     2. Data Management with Biostatics and Medical coding 

     3. Project Management 

     4. Clinical Trial Monitoring 

     5. Medical Writing 

     6. Pre-Post Regulatory Support 

     7. Computer System Validation 

     8. IT Auditing 

     9. CRO Set up 

    10. SOP Management 

    11. Quality Assurance 

    12. GxP Training.

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