Unrecognise Training Provided By Other Parties Other Than Medical Device Authority In Relation To The Medical Device Act 2012 (Act 737) And Medical Device Regulatory Requirements

We notice that some companies are offering training on regulatory requirements of Act 737 including GDPMD. We would like to emphasise that any regulatory training under Act 737 is part of MDA Training Programme. We have never given any authority to anyone or any company to conduct such training and we shall not be liable for any inaccuracies or misinterpretations of the contents of the training conducted by parties other than MDA. MDA also will not recognise any training on regulatory requirements of Act 737 provided by other parties.

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