{"id":198,"date":"2016-08-01T10:52:25","date_gmt":"2016-08-01T08:52:25","guid":{"rendered":"https:\/\/www.iqsqualitysystems.co.za\/?p=198"},"modified":"2024-01-12T12:26:07","modified_gmt":"2024-01-12T10:26:07","slug":"mcc-news","status":"publish","type":"post","link":"https:\/\/www.iqsqualitysystems.co.za\/mcc-news\/","title":{"rendered":"MCC News"},"content":{"rendered":"

The Medical Control Council held a workshop last week in respect of the new legislation for medical devices and IVDs.<\/p>\n

Initially the companies and organisations who need to comply will be required to apply for a licence.  Only later will they registration of products take place.<\/p>\n

You will either need a licence to manufacture or a licence to distribute – if you do not manufacture the product.<\/p>\n

There is a list of documents and criteria that need to be supplied when you apply for your licence, including proof of ISO 13485 compliance.  If you need any help, please contact me.<\/p>\n

 <\/p>\n","protected":false},"excerpt":{"rendered":"

The Medical Control Council held a workshop last week in respect of the new legislation for medical devices and IVDs. Initially the companies and organisations who need to comply will be required to apply for a licence.  Only later will they registration of products take place. 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