Combination products
The course is aimed at those with regulatory knowledge in Pharma and a need for a better understanding of medical devices and the requirements of the European regulation, Medical Device Regulation (MDR)....
GAMP 5
...have gained an overview of the content of GAMP 5 with a focus from the perspective of you as specifier, purchaser, supplier and manager of system solutions, for GxP and MDR regulated activities....
ISO 13485
...Changes compared to the previous edition of ISO13485 and the link to MDR. After the training, you should have gained knowledge of the standard and the changes in the 2016 version. You also have good...
