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DRDDO
Dear All
Frankly, it is not my concern, because some medical device importers in Thailand ask me this interesting question.
As all of you know, ISO 13485, requires some document call DMR (device master record), so, for ISO 13485 certified-medical device-importer (from overseas to sales in Thailand), they must have DMR; the problem is what kind of DMR or document must or shall or should they have? Advice needed.
DRDDO
Frankly, it is not my concern, because some medical device importers in Thailand ask me this interesting question.
As all of you know, ISO 13485, requires some document call DMR (device master record), so, for ISO 13485 certified-medical device-importer (from overseas to sales in Thailand), they must have DMR; the problem is what kind of DMR or document must or shall or should they have? Advice needed.
DRDDO
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