Advantages of Zenovel

  • Tailored made service packages offered and make the trial cost effective
  • Ethics, quality and customer satisfaction is the prime focus in our mind
  • Well trained experienced staff dedicated for CGP, GMP and Regulatory services
  • Collective monitoring of approx. 700 study monitoring across globe
  • Expertise in handling study of wide therapeutic range
  • Expertise in handling study of wide therapeutic range Experience of facing regulatory inspections like EMA, USFDA, WHO, DCGI & more
  • Successfully completed CRO development from scratch to first study submission
  • Hands on Data integrity concept and utilization in the clinical research
  • Zenovel has the presence across the globe and well positioned to serve client in any country.
  • Structured SOP and quality driven system in place
  • Successfully handled regulatory queries and responses
  • Acknowledgement of service standards amongst the regulatory inspectors
  • Designed complex trial and helped to complete it successfully
  • Providing high quality monitoring report and checklists timely manner
  • Expertise in handling deviation and CAPA managements on site
  • Root cause analysis with advance tool and designing way forward
  • Practicing Risk based monitoring approach
  • Expertise in development of difficult Bioanalytical method and validation
  • Bird eye on advance technology and regulatory upgradation to be on track
  • Committed to live up to expectation of client
  • Expert review of Pharmacokinetic and Statistical analysis data

We are happy to help. Reach us at: +91-635-635-3636 , [email protected]

Check Our Method Directory