Comprehensive clinical trial delivery across Phase I–III with a focus on quality and efficiency.
Teja brings 12 years’ experience of working in a number of QA GCP roles in the Clinical research & CRO industry.
She has extensive experience in conducting GCP & GCLP audits, supplier audits and hosting external inspections. She has led multiple projects involving improvement of existing processes and systems, implementation of GCP compliant standards within business and regulatory gap analysis.
She has worked at hVIVO since 2016 and was appointed as Head of QA in 2021. Previously she worked as a GCP Compliance manager at Institute of Cancer Research/Royal Marsden Hospital.
Teja is a pharmacist and holds M. Tech degree in Bioprocess Technology and Doctorate degree in Pharmaceutical Sciences from University of Mumbai, India.
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