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