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