November 2020 | CMS MedTech

Medical Device registration in Indonesia

By cmsmedtech November 22, 2020Indonesia

https://www.youtube.com/watch?v=f22ggDfIFwE Medical Device registration in Indonesia: Requirements 1 Regulatory Approval from GHTF Countries such as 510(k) / TGA / CE etc. if applicable. FORM A 2 Medical Devices Distributor License…

Common Specifications

By cmsmedtech November 10, 2020CE, common specifications

CS Links Commission Implementing Regulation (EU) 2020/1207 of 19 August 2020 laying down rules for the application of Regulation (EU) 2017/745 of the European Parliament and of the Council as…

Easy Guide on how to comply to MDR and ISO 13485

Free ISO 13485 Feedback and Complaint Handling Template

By cmsmedtech November 1, 2020ISO 13485

Free ISO 13485 Feedback and Complaint Handling Template You can buy the ISO 13485 standard here. Email us here to get and type "CMSfeedback" in the email message to get our free template…

Medical Device registration in Indonesia

Common Specifications

Free ISO 13485 Feedback and Complaint Handling Template

EXTENSION OF THE MDR TRANSITIONAL PERIOD AND REMOVAL OF THE ‘SELL OFF’ PERIODS

Medical Device Registration in Thailand

Medical Device Registration Vietnam (updated 2023)

Medical Device Registration in UK

Medical Device Registration in New Zealand