MHRA guidance – Assistive technology: definition and safe use
More from GuidanceMore posts in Guidance »
- EU – MDCG 2020-5 Clinical Evaluation – Equivalence. A guide for manufacturers and notified bodies
- EU – Guidance on temporary extraordinary measures related to medical device Notified Body audits during COVID-19 quarantine orders and travel restrictions
- US – FDA Issues Immediately in Effect Guidance on Ventilators During COVID-19
- UU – Final guidance – Premarket Notification (510(k)) Submissions for Electrosurgical Devices for General Surgery
- US Final Guidance – Bone Anchors – Premarket Notification (510(k)) Submissions
More from Medicines and Healthcare Products Regulatory Agency - MHRAMore posts in Medicines and Healthcare Products Regulatory Agency - MHRA »
- UK – Independent Medicines and Medical Devices Safety Review report and MHRA response
- UK – MHRA – Effective field safety notices (FSNs): guidance for manufacturers of medical devices
- UK – Medicines and Medical Devices Bill: overarching documents
- UK – MHRA revised guidance – Guidance Notified bodies for medical devices
- MHRA Revised Guidance – Clinical investigations of medical devices – guidance for manufacturers
Be First to Comment