New cycle and start for the EUCRAF Certificate Programme 2015/2017
In an increasingly global market with New Biopharmaceuticals Entities (NBEs) gaining more attention in research and development, understanding the regulations and guidelines is more important than ever.
In response to industry needs, the Certificate Programme at EUCRAF provides training to regulatory affairs professionals on the special regulatory requirements needed for a successful marketing authorization of biopharmaceuticals.
The next cycle of the Postgraduate Certificate Programme as “Regulatory Affairs Manager” will start with Seminar 1 on the 15th Septmeber 2015.
To our new participants, here are 3 tips for getting the most out of the program:
- Develop a study schedule. It is important to develop a detailed calendar to note the seminars and mark out regular study time. A planned outline will enable you to stay focused and helps you to meet your goals.
- Ask questions and take advantage of meeting the experts in the seminars. They bring a wealth of knowledge and experience and tap into their expertise for any concerns you may have.
- Build your network with the speakers and fellow participants. Networking is an important skill for career success. Your regulatory friends can help you in your career, especially in sharing experiences and knowledge about regulatory topics and challenges.
If you have any questions, feel free to contact us for information. We look forward to working with all of you in the next programme cycle!
Your EUCRAF Team