Global Regulatory Affairs for Medical Products

 

Regulatory affairs

 

About the course

This online course introduces the participants to the quality systems used to meet the regulatory requirements for developing, testing, manufacturing, and selling medical products in the global marketplace. It provides a general background for all employees in the medical products field, but it is especially useful to participants preparing for a career in the Regulatory Affairs or Quality Assurance departments within a pharmaceutical, biomanufacturing, or medical device company

Who is this course for

The course is intended for participants interested in global regulatory affairs, e.g. employees in the medical products field, especially at the entry stage to a career in the Regulatory Affairs or Quality Assurance departments within a pharmaceutical, biomanufacturing, or medical device company.

 

This course has been developed in the framework of the NNF funded project AIM-Bio, in collaboration between DTU Bioengineering, DTU Chemical Engineering and Biomanufacturing Training and Education Center (BTEC) at North Carolina State University.

 

Practical Information for participants.

Contact

Anne Margrethe Dahl Nielsen
Continuing Education Coordinator
DTU Bioengineering
+45 93 51 01 76

Practical Information

Info on course dates and registration coming soon