Masunga R Mkangala

• Dispensed prescribed medicines accurately and provided counselling on rational drug use to patients. • Participated in ward rounds, contributing to patient treatment plans and monitoring medication therapy outcomes. • Supported antimicrobial stewardship programs by promoting rational antibiotic use and monitoring resistance trends. • Contributed to pharmacovigilance by detecting, documenting, and reporting Adverse Drug Reactions (ADRs). • Assisted in inventory and supply chain management, ensuring availability of essential medicines. • Collaborated with healthcare professionals to improve patient safety and therapeutic outcomes.

• Conducted technical reviews of regulatory dossiers for medicines and medical devices (registrations, renewals, and variations) ensuring compliance with TMDA guidelines. • Assisted in premises inspection and registration of pharmaceutical businesses. • Supported pharmacovigilance activities, including ADR and AEFI causality assessments, and public awareness campaigns. • Contributed to risk assessments and regulatory compliance monitoring of pharmaceutical products. • Participated in quality control and post-market surveillance activities. • Participated in capacity building training on dossier assessment and compliance monitoring.

• Prepared and reviewed medication orders to ensure accuracy, safety, and compliance with treatment guidelines. • Dispensed medications and provided counseling to patients on proper drug usage, dosage, and side effects. • Conducted stock taking, inventory management, and maintained accurate stock balance records to prevent shortages and expiries. • Supervised pharmacy technicians and support staff to ensure efficient pharmacy operations and quality service delivery. • Maintained proper documentation of prescriptions, stock records, controlled drugs, and pharmacy reports. • Participated in community outreach programs, including patient screening, health education, and medication awareness campaigns. • Performed patient testing and screening services during outreach activities and referred patients for further management when necessary. • Monitored medication availability and coordinated procurement requests to maintain uninterrupted pharmaceutical services. • Participated in Hospital Therapeutic Committee meetings to discuss medication use, treatment protocols, and rational drug management. • Ensured compliance with pharmaceutical regulations, hospital policies, and professional standards. • Collaborated with healthcare professionals to optimize patient treatment outcomes and improve medication management. • Assisted in pharmacovigilance activities by monitoring and reporting adverse drug reactions and medication-related issues.

• Prepare and compile scientific dossiers for product registration in compliance with Tanzania Medicines and Medical Devices Authority regulatory requirements. • Conduct follow-ups with Tanzania Medicines and Medical Devices Authority regarding product registration status, approvals, and regulatory submissions. • Assist with preparation and submission of import permit applications for pharmaceutical and medical products. • Conduct pharmacovigilance activities, including monitoring, documenting, and reporting adverse drug reactions and product safety information. • Coordinate importation processes and monitor imported products from shipment to final arrival and clearance. • Ensure imported products comply with local regulatory guidelines, documentation requirements, and quality standards. • Maintain accurate regulatory documentation, records, and correspondence related to registered and imported products. • Collaborate with suppliers, clearing agents, and regulatory authorities to ensure smooth and timely product importation. • Support regulatory compliance activities to ensure products meet national pharmaceutical regulations and standards. • Assist in post-market surveillance activities and regulatory reporting requirements.

• Conduct client outreach and engage with medical device manufacturers seeking market entry into East Africa. • Communicate and coordinate with local distributors to connect them with international clients and facilitate business partnerships. • Prepare and compile regulatory dossiers for medical device registration in compliance with Tanzania Medicines and Medical Devices Authority requirements. • Conduct follow-ups with Tanzania Medicines and Medical Devices Authority regarding product registration status, approvals, and regulatory submissions. • Support clients with regulatory guidance and compliance requirements for medical device registration and importation. • Coordinate submission of regulatory documents and maintain accurate records of applications and approvals. • Liaise with manufacturers, distributors, and regulatory authorities to ensure smooth product registration and market access processes. • Monitor regulatory timelines and provide updates to clients regarding registration progress and compliance matters. • Assist in market entry activities by identifying potential distribution partners and facilitating introductory meetings. • Maintain professional relationships with healthcare stakeholders, suppliers, and business partners to support company growth and client expansion.