Medicines and Healthcare Products Regulatory Agency Annual Report and Accounts 2018 to 2019
Medical Device Expert News
Digital Health Update: Mid-Year Update on Software Precertification Program
Dental radiographic X-ray imaging: dose to patients
Programmable CSF Shunts and Magnetic Field Interference with Implanted Hearing Devices – Letter to Health Care Providers
MHRA launches consultation on how to best engage patients and the public
IMDRF terminologies for categorized Adverse Event Reporting (AER): terms, terminology structure and codes (Edition 4) – Annex А (Edition 3), G
Preventing Medical Device Shortages by Ensuring Safe and Effective Sterilization in Manufacturing Device Shortages Update: The FDA Announces Two New Innovation Challenges on Device Sterilization…
How the FDA Uses Science to Speed Medical Device Innovation
US FDA Develops and Qualifies First Non-Clinical Assessment Model Tool as Part of the MDDT Program – MDDT SUMMARY OF EVIDENCE AND BASIS OF QUALIFICATION…
Danish Medicines Agency strengthens its policy on conflicts of interest