Why 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 , bd@zenovel.com