mitigation plans in place to engage. Regulatory authorities when earliest signs of delay emerge. Proactively standards in the following process areas: Marketing Authorization Applications License maintenance e.g., Renewals Labelling and Artwork Management Robust Health Authority interactions To track and manage all GRP activities job profile. Marketing Authorization Applications: Submit Marketing Authorization Applications to the SA SA Health Authority according to SA HA guidelines and GRP, in the shortest possible time based on business
maintenance in accordance with the latest regulatory authority requirements. Registered with the South African skills. Thorough knowledge of world-wide Health Authority requirements on Regulatory technical format including skills. Thorough knowledge of world-wide Health Authority requirements on Regulatory technical format including compliance with the relevant Health Regulatory Authorities, Medicines, and Related Substances Control Act regulatory affairs or experience at a health authority. Implement a registration plan and provide business
maintenance in accordance with the latest regulatory authority requirements. Registered with the South African skills. Thorough knowledge of world-wide Health Authority requirements on Regulatory technical format including skills. Thorough knowledge of world-wide Health Authority requirements on Regulatory technical format including compliance with the relevant Health Regulatory Authorities, Medicines, and Related Substances Control Act regulatory affairs or experience at a health authority. Implement a registration plan and provide business
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
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
before domestic or international regulatory authorities on major policy matters.
the South African Health Products Regulatory Authority (SAHPRA) as well as the current guidelines and
the South African Health Products Regulatory Authority (SAHPRA) as well as the current guidelines and
Managing and coordinating response to the regulatory authority. Maintain regulatory knowledge of the various