PROTECTING YOUR RIGHT TO MEDICINES AND MEDICAL DEVICES
Friday, 24 November 2017
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Frequently Asked Question

14.Should the manufacturing site of the complementary medicine be inspected before the product is registered?

The Authority requires that the all premised where manufacturing occurs conforms to some standard of cGMP. The Authority is aware that some countries do not inspect manufacturers of some products, however evidence of a standard of cGMP is required. The MCAZ may insist that its inspectors inspect the site on a case by case basis.