Lubna Rajiwate, MSc

Regulatory Affairs Practice – Europe

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.