curtailed. - Cultivate robust relationships with authorities, guaranteeing legal compliance and shared ecological internal compliance audits with precision and authority. - Enhance the company's environmental management
curtailed. - Cultivate robust relationships with authorities, guaranteeing legal compliance and shared ecological internal compliance audits with precision and authority. - Enhance the company's environmental management
compliance with the relevant medicine Regulatory Authorities (Country Specific where applicable), Medicines applications for submission to the regulatory authorities Work in collaboration with internal and external maintain effective relationships with Regulatory Authorities, internal and external stakeholders Formulate
regulations and standards set by the relevant authorities. Key Responsibilities: Develop and maintain relationships relationships with regulatory authorities to ensure timely approvals for new products and variations
regulations and standards set by the relevant authorities. Key Responsibilities: Develop and maintain relationships relationships with regulatory authorities to ensure timely approvals for new products and variations
compliance with the relevant Medicine Regulatory Authorities (Country Specific where applicable), including the South African Health Products Regulatory Authority (SAHPRA) and South African Pharmacy Council (SAPC)
between the business, clients and regulatory authorities. Minimum requirements for the role: Must have before domestic or international regulatory authorities on major policy matters. Reviewing all regulatory customers. Developing relationships with regulatory authorities to analyze potential impacts of proposed environmental
between the business, clients and regulatory authorities. Minimum requirements for the role: Must have before domestic or international regulatory authorities on major policy matters. Reviewing all regulatory customers. Developing relationships with regulatory authorities to analyze potential impacts of proposed environmental
requests on all drug safety matters from Regulatory Authorities for product portfolio. Support the collation requests on all drug safety matters from Regulatory Authorities. Involvement in the development of Risk Management bid defence meetings. Previous experience with authoring/reviewing PV procedures is preferred. Experience
requests on all drug safety matters from Regulatory Authorities for product portfolio. Support the collation requests on all drug safety matters from Regulatory Authorities. Involvement in the development of Risk Management bid defence meetings. Previous experience with authoring/reviewing PV procedures is preferred. Experience