Courses and events progression pathway

Regulatory affairs career progression pathway graphic

 

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Drive your regulatory career

Courses at this level are for people at senior level taking on additional responsibilities or looking to diversify their skills.
Begin DateTitleDescription
16/09/2025Regulatory Requirements for Cell Tissue & Gene TherapiesModule 22 of the MSc and Masterclass: Designed for regulatory affairs professionals to develop and deepen their understanding of all aspects of the regulation of advanced therapy medicinal products, which has grown in significance over the past five years. It fills a gap in the educational needs for contemporary regulatory affairs specialists. It will allow students to examine the regulatory requirements for advanced therapy medicinal products in the EU and compare this with other territories. It will consider the scientific principles underpinning the development and regulation of advanced therapy medicinal products and the complexities involved.
16/09/2025Regulatory Requirements for Cell Tissue & Gene TherapiesModule 22 of the MSc and Masterclass: Designed for regulatory affairs professionals to develop and deepen their understanding of all aspects of the regulation of advanced therapy medicinal products, which has grown in significance over the past five years. It fills a gap in the educational needs for contemporary regulatory affairs specialists. It will allow students to examine the regulatory requirements for advanced therapy medicinal products in the EU and compare this with other territories. It will consider the scientific principles underpinning the development and regulation of advanced therapy medicinal products and the complexities involved.
12/05/2025The EU Paediatric RegulationThis Masterclass provides an understanding of legislation ensuring that medicines for children are high quality, ethically researched, and appropriately authorised. It is also Module 23 of the MSc.
12/05/2025The EU Paediatric RegulationThis Masterclass provides an understanding of legislation ensuring that medicines for children are high quality, ethically researched, and appropriately authorised. It is also Module 23 of the MSc.
30/07/2025Regulatory Environment in the Middle East and North AfricaThis Masterclass provides an understanding of the regulatory landscape in the Middle East and North Africa. It is also Module 24 of the MSc.
30/07/2025Regulatory Environment in the Middle East and North AfricaThis Masterclass provides an understanding of the regulatory landscape in the Middle East and North Africa. It is also Module 24 of the MSc.
07/10/2025The Regulatory Environment in South/East AsiaThis Masterclass will provide you with an understanding of the regulatory landscape across South/East Asia. This Masterclass is also Module 25 of the MSc.
07/10/2025The Regulatory Environment in South/East AsiaThis Masterclass will provide you with an understanding of the regulatory landscape across South/East Asia. This Masterclass is also Module 25 of the MSc.
10/11/2025Leadership and Strategic Management in Regulatory AffairsThis Masterclass is designed for regulatory affairs professionals to develop their understanding of the management and leadership skills needed to run a successful regulatory affairs department/organisation.  The course is designed to be applicable to both drugs and device regulatory affairs by applying the principles taught to your own particular environment. This Masterclass is also Module 10 of the MSc.
10/11/2025Leadership and Strategic Management in Regulatory AffairsThis Masterclass is designed for regulatory affairs professionals to develop their understanding of the management and leadership skills needed to run a successful regulatory affairs department/organisation.  The course is designed to be applicable to both drugs and device regulatory affairs by applying the principles taught to your own particular environment. This Masterclass  is also Module 10 of the MSc.
18/11/2025Data Management and Digitalisation in Regulatory AffairsThis Masterclass will provide you with  the theoretical background to data management, document management, electronic submissions, eCompliance regulatory information management and the new identification of Medicinal Products (IDMP) requirements, and find solutions to practical problems in this area. Deal with large volumes of data and deal with different data (from nonclinical to post-market pharmacovigilance). This Masterclass is also Module 12 of the MSc.
18/11/2025Data Management and Digitalisation in Regulatory AffairsThis Masterclass will provide you with  the theoretical background to data management, document management, electronic submissions, eCompliance regulatory information management and the new identification of Medicinal Products (IDMP) requirements, and find solutions to practical problems in this area. Deal with large volumes of data and deal with different data (from nonclinical to post-market pharmacovigilance). This Masterclass is Module 12 of the MSc.
01/04/2025Regulatory Strategy for Established Active SubstancesThis Masterclass is designed for regulatory affairs professionals to develop and deepen their understanding of all aspects of the regulation of and the strategic issues to be considered in relation to medicines containing established active substances, including line extensions, generics and the relevant aspects for over-the-counter (OTC) products. It will allow them to examine the regulatory requirements imposed on these substances. This Masterclass  is also Module 7 of the MSc.
01/04/2025Regulatory Strategy for Established Active SubstancesThis Masterclass is designed for regulatory affairs professionals to develop and deepen their understanding of all aspects of the regulation of and the strategic issues to be considered in relation to medicines containing established active substances, including line extensions, generics and the relevant aspects for over-the-counter (OTC) products. It will allow them to examine the regulatory requirements imposed on these substances. This Masterclass is also Module 7 of the MSc.

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