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
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
Managing and coordinating response to the regulatory authority. Maintain regulatory knowledge of the various
Managing and coordinating response to the regulatory authority. Maintain regulatory knowledge of the various
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
submit reports to management and regulatory authorities on SHEQ performance, including key metrics, trends