Getz Pharma
Sitara Luqman is an experienced professional in regulatory management and pharmacy, currently serving as Assistant Manager Regulatory Management at Getz Pharma since January 2021, where responsibilities include overseeing regulatory activities for medical devices and health products. Prior experience includes a role as Senior Executive in Regulatory Management at Getz Pharma Private Limited, where tenure began in December 2017, and as a Regulatory Affairs Officer at A. Feroz & Co., Private Limited. Additionally, Sitara's background includes serving as a Quality and Patient Safety Officer at Chiniot General Hospital and an Internee Pharmacist at OMI Hospital. Educational qualifications comprise a Doctor of Pharmacy degree from Dow University of Health Sciences and a certification as a Clinical Research Professional.
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Getz Pharma
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Getz Pharma is one of the leading pharmaceutical companies whose manufacturing facility is pre-qualified and approved by the World Health Organization (WHO), Geneva, as well as from member countries of the Pharmaceutical Inspection Co-operation Scheme (PIC/S). Getz Pharma is the only pharmaceutical manufacturing company in entire South Asia to achieve the LEED (Leadership in Energy and Environmental Design) Platinum Certification from the U.S. Green Building Council (USGBC).