Let’s work together Tittle Mr. Mrs Dr Ms. Miss First Name Last Name Email * Phone (###) ### #### What services are you interested in? New product dossier compilations in CTD, eSubmission and eCTD for human Orthodox Medicines- New Chemical Entities, Biologicals, Biosimilars, Vaccines Application of CTD, eSubmission and eCTD for Orthodox Medicines- Generics based on Bioequivalence studies, clinical data and biowavers. Application of CTD for Complementary Medicines Due diligence on dossier information. Pharmaceutical Variations including full conversations from MBR1 and MRF1 to current eSubmission and eCTD Application for registration for veterinary medicines under Act 101 and Act 36. GMO Applications Compilation of Pharmacovigilance master file (PMF) Responsible person for pharmacovigilance for both pre- and post- marketing surveillance Establishing and maintaining the local PV system in accordance with legal requirements, corporate standards and best practice within the pharmaceutical industry. Collect product medical information Pricing and Reimbursement Strategies Health Economics SMF, Quality Manual cGMP, ISO and Audits QMS and SOPs Technical Contracts Responsible Pharmacist SADC, EAC and Other African Countries Other - SAHPRA Additional Comments Thank you! GET IN TOUCHEmail: mzondi@zondmolpharma.co.zaContact Number: +27 82 332 3325Vorna Vally Midrand1686
