NEW CIRCULAR LETTER OF THE MEDICAL DEVICE AUTHORITY NO. 3 YEAR 2017 (IMPLEMENTATION AND ENFORCEMENT OF GUIDELINE FOR REGISTRATION OF DRUG-MEDICAL DEVICE AND MEDICAL DEVICE-DRUG COMBINATIONS PRODUCTS)

 

The purpose of this circular is to set the implementation and enforcement under the Medical Device Act 2012 ( Act 737) relating to medical devices that fall under the definition of Combination Product as defined in the Guideline For Registration of Drug-Medical Device and Medical Device-Drug Combination Products.

To view Circular Letter of The Medical Device Authority No. 3 Year 2017 CLICK HERE

To view Guideline For Registration of Drug-Medical Device and Medical Device-Drug Combination Products CLICK HERE