OVERVIEW
FOCUS AREAS
More than 16 years of regulatory experience managing global clinical trial applications.
Regulatory strategy
Operational efficiencies
Regional SME
A regulatory professional with extensive experience in clinical study start up and regulatory aspects of clinical research while handling global clinical trial and marketing authorization applications.
Lubna is a highly motivated and result oriented clinical regulatory professional. Lubna has extensive experience in developing regulatory strategy, product development, clinical trial management systems, risk assessment and managing change within regulatory functions.
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EDUCATION:
- Bachelor in pharmacy, University of Pune, India
- Masters in Clinical Research, Cranfield University, UK
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