Ramadhianti M

Regulatory Affairs

Ramadhianti M has a comprehensive background in pharmacy and regulatory affairs, currently serving in the Regulatory Affairs department at AstraZeneca since March 2022. Responsibilities include managing new drug product submissions within the cardiovascular and renal metabolic (CVRM) therapeutic area, overseeing registration variations and renewals for numerous CVRM and respiratory products, and ensuring compliance with BPOM regulations. Previous experience includes roles as a Clinical Pharmacist at PT. Kimia Farma Apotek and RSUP Dr. Hasan Sadikin, where Ramadhianti screened drug prescriptions and analyzed therapy regimens to prevent medication errors. Ramadhianti also worked in Quality Assurance at PT. Caprifarmindo Laboratories, focusing on pharmaceutical product development processes. Academic qualifications include a Professional Pharmacy Student degree and a Bachelor of Pharmacy from Institut Teknologi Bandung.

Location

South Jakarta, Indonesia

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