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Guideline For Premedical Device And Medical DeviceDrug Combination ProductsMINISTRY OF HEALTH MALAYSIAGUIDELINE FOR PREMEDICAL DEVICE AND MEDICAL DEVICEDRUG COMBINATION PRODUCTS ENDORSEMENT LETTER
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The guideline for registration of provides instructions and requirements for registering a particular item or service.
Any individual or entity who wishes to register the specific item or service is required to file the guideline for registration.
The guideline for registration must be filled out accurately and completely, following the instructions provided in the document.
The purpose of the guideline for registration is to ensure that the registration process is carried out efficiently and in compliance with all regulations.
The guideline for registration must include all relevant information about the item or service being registered, as well as any supporting documentation required.
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