Pharmaceutical regulations vary by region and country making regulatory planning and strategy challenging for professionals. Many countries have specific regulations, processes and procedures that must be understood to overcome regulatory hurdles. Training is critical for those working with unfamiliar regulatory agencies. Our courses focus on specific countries or regions that your trying to get your products registered into. The training we deliver draws comparisons with regions you are already familiar with such as the FDA or EMA. This helps you best utilise your current set up to ensure efficient cross over.
We offer courses in the following areas: Regulatory Affairs in LATAM | Regulatory Affairs in China | Regulatory Affairs in MENA | Regulatory Affairs in Russia & CIS | Regulatory Affairs in Japan | Regulatory Affairs in APAC
We support regulatory affairs leaders improve the technical skills and knowledge of their employees, so they are equipped to overcome challenges and meet business objectives. Working together, we design and deliver technical training courses that align with your learning requirements and business goals. For more information about how we can support your team please get in touch.
Could your team benefit from a bespoke regulatory course on a specific region or country? We would be happy to discuss your objectives and see how we might be able to help.