Public Consultation on EMA Draft Q&A: Co-Processed Excipients in Solid Oral Dosage Forms The European Medicines Agency (EMA) has published the draft questions and answers regarding co-processed excipients used in solid oral dosage forms for public consultation. Public Consultation on EMA Draft Q&A: Co-Processed Excipients in Solid Oral Dosage Forms
2024 DSIT Research and Innovation Workforce Survey The Department for Science, Innovation and Technology (DSIT) is conducting the 2024 Research and Innovation (R&I) Workforce Survey. The results will impact UK government policy and R&D funding decisions. 2024 DSIT Research and Innovation Workforce Survey
13th Notified Body Designated Under the EU MDR Italy-based notified body ‘ISTITUTO SUPERIORE DI SANITA' has been notified as the 13th Notified Body under the MDR. 13th Notified Body Designated Under the EU MDR
MHRA Consultation on Statutory Fees Proposals MHRA has launched a consultation on proposals to update the MHRA's statutory fees to ensure they continue to recover their costs. MHRA Consultation on Statutory Fees Proposals
MHRA Clinical Investigation for Medical Devices – QSR Template MHRA has added a new Quarterly Summary Reports (QSR) template to the guidance 'Notify MHRA about a clinical investigation for a medical device'. MHRA Clinical Investigation for Medical Devices – QSR Template
BHMA – Meet the BAPP Best Practices SOP Webinar BHMA in collaboration with ABC, AHP and NCNPR are hosting a webinar introducing the BAPP Best practices SOP on Tuesday 1 October at 4pm. BHMA – Meet the BAPP Best Practices SOP Webinar
MHRA AI Airlock – Webinar Recording Available In July, MHRA hosted a webinar on AI Airlock. The recording of this webinar has been published. MHRA AI Airlock – Webinar Recording Available
Defra- Extended Producer Responsibility (EPR) Fees Webinar Defra is hosting a webinar on EPR Fees. Defra- Extended Producer Responsibility (EPR) Fees Webinar
MHRA – Invoicing System Issue MHRA has discovered there is currently an IT issue which is causing the issuing of incorrect invoices. MHRA – Invoicing System Issue
Notify MHRA about a Clinical Investigation for a Medical Device – Regulatory Advice Meetings MHRA has updated the guidance on how to notify the MHRA of your intention to carry out a clinical investigation for medical devices to add a section on regulatory advice meetings. Notify MHRA about a Clinical Investigation for a Medical Device – Regulatory Advice Meetings
MHRA Medical Devices Registration System Updates MHRA has updated the Account Management Reference Guide, Device Registration Reference Guide and Certificates of Free Sale for Medical Devices guidance to reflect changes to the registration system. MHRA Medical Devices Registration System Updates
UK Environmental Improvement Plan The UK Government has publishes the Environmental Improvement Plan (EIP) Annual Progress Report. UK Environmental Improvement Plan
