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