Team NB Position Paper on Hybrid Audits Team NB Position Paper on Hybrid Audits Team NB has published a position paper on the application of hybrid audits... Team NB Position Paper on Hybrid Audits
Commission Proposal on Single Market Emergency Instrument Published Commission Proposal on Single Market Emergency Instrument Published The European Commission has tabled a legal proposal establishing... Commission Proposal on Single Market Emergency Instrument Published
33rd Notified Body has been designated under the EU MDR Poland-based Notified Body ‘POLSKIE CENTRUM BADAN I CERTYFIKACJI S.A.’ has been notified as the 33rd Notified Body under the EU... 33rd Notified Body has been designated under the EU MDR
DHSC Webinar Replay – Equity in Medical Devices: Independent Review Call for Evidence DHSC Webinar Replay – Equity in Medical Devices: Independent Review Call for Evidence DHSC held a webinar on Wednesday 7... DHSC Webinar Replay – Equity in Medical Devices: Independent Review Call for Evidence
MHRA Webinar – Changes to the Submission Routes for Reporting Medical Device Adverse Incidents MHRA Webinar – Changes to the Submission Routes for Reporting Medical Device Adverse Incidents Following the postponement of the ‘Changes... MHRA Webinar – Changes to the Submission Routes for Reporting Medical Device Adverse Incidents
EU IVDR Implementation – Final MDCG Guidance on Appropriate Surveillance Regarding the Transitional Provisions under Article 110(3) Published EU IVDR Implementation – Final MDCG Guidance on Appropriate Surveillance Regarding the Transitional Provisions under Article 110(3) Published The European... EU IVDR Implementation – Final MDCG Guidance on Appropriate Surveillance Regarding the Transitional Provisions under Article 110(3) Published
MHRA Updates Software Applications (Apps) Guidance MHRA updates its guidance on software applications (apps) MHRA has updated its guidance on when software applications are considered to... MHRA Updates Software Applications (Apps) Guidance
EU IVDR Implementation – MDCG Guidance Providing Clarification on First Certification of Type of Device Revised Version Published EU IVDR Implementation – MDCG Guidance Providing Clarification on First Certification of Type of Device Revised Version Published A revised... EU IVDR Implementation – MDCG Guidance Providing Clarification on First Certification of Type of Device Revised Version Published
MHRA Annual Report and Accounts 2021 – 2022 – PAGB’s Key Points 0 Share: Share via Facebook... MHRA Annual Report and Accounts 2021 – 2022 – PAGB’s Key Points
MHRA Webinar – Changes to the Submission Routes for Reporting Medical Device Adverse Incidents MHRA Webinar – Changes to the Submission Routes for Reporting Medical Device Adverse Incidents Adverse incidents involving medical devices that... MHRA Webinar – Changes to the Submission Routes for Reporting Medical Device Adverse Incidents
Government Response to MHRA Consultation on a New Code of Practice for the Expert Advisory Committees Published Government Response to MHRA Consultation on a New Code of Practice for the Expert Advisory Committees Published The government have... Government Response to MHRA Consultation on a New Code of Practice for the Expert Advisory Committees Published
Borderline Manual under MDR and IVDR Published Borderline Manual under MDR and IVDR Published The European Commission has published the Manual on borderline and... Borderline Manual under MDR and IVDR Published
