regulatory standards Co-ordination and submission of new product applications in South Africa and other applicable implementation plans for the preparation and submission of new products Conduct dossier due diligence to ensure pertaining to the pharmaceutical industry. Internal training and mentoring Establish and maintain effective
attendance / participation at key internal meetings/training sessions, relevant congresses, and seminars and Ownership of pre-launch medical activities (BD, new products assessments, market research program, advisory Conduct medical and product training for medical representatives (Initial training, Refreshment sessions, such as key areas of scientific/company interest, new trends in diagnosis, monitoring and treatments in
adherence to timelines Plan, coordinate and drive new product launch activities Plan, coordinate and drive characteristics are agreed and documented for all new and reformulated products Investigate raw material ensure execution of process validation protocols for new products/reformulated products/current products Compile study protocols and temperature cycling studies for new products/reformulated products/current products Communicate
adherence to timelines Plan, coordinate and drive new product launch activities Plan, coordinate and drive characteristics are agreed and documented for all new and reformulated products Investigate raw material ensure execution of process validation protocols for new products/reformulated products/current products Compile study protocols and temperature cycling studies for new products/reformulated products/current products Communicate
Implement / facilitate Generic and Core Competency training and coaching in all Sections. Comply with OHS