Check out the details for the new option for getting innovative Medical products to market. https://lnkd.in/eRTneiaW
News
SLCP Training
Our team in the Indian Ocean has successfully completed two SLCP deep dive training recently. One session was done with the social compliance, sustainability and learning teams in Madagascar. The second session in Mauritius included key players in the apparel and food industry as well…
Deep-dive training season on SLCP Verification by International Associates
Event by International Associates Limited Fri, Nov 10, 2023, 9:00 AM – 3:30 PM (your local time) Uttara Model Town, Dhaka, BD Sea Shell Hotel, House-09, Road -13, Sector-10, Event link https://www.ia-uk.com/deep-dive-slcp-training-7/
SA8000 Basic Auditor Course – London
Event by International Associates Limited Oct 9, 2023, 1:30 PM – Oct 13, 2023, 9:30 PM (your local time) London, England, GB
White Paper Medical Device Labeling
Marking and Labelling is one of our client’s most asked-about topics of the MDR (Medical Device Regulations) We have put together a handy white paper for reference. https://www.ia-uk.com/wp-content/uploads/2023/09/1694158801309.pdf S P E A K T O A C O N S U L T A N…
The EU Commission some feedbacks
Why not give the EU Commission some feedback on their communication and the new MDR extension The objective of the online survey is to better understand the information needs around the EU Regulations on medical devices (MDR) and in vitro diagnostic medical devices (IVDR). particularly…
The EU Commission’s Q&A
The EU Commission’s Q&A on practical aspects related to the implementation of Regulation (EU) 2023/607 amending Regulations (EU) 2017/745 and (EU) 2017/746 as regards the transitional provisions for certain medical devices and in vitro diagnostic medical devices that were released in July has a handy…
The European Commission published
On 18 July, the European Commission published in the Official Journal of the European Union an updated guideline made up of Questions and Answers on the practical aspects related to the implementation of Regulation as they relate to the SCOPE OF THE EXTENSION OF THE…
SA8000 training course
Check out our next SA8000 training course dates for London UK https://lnkd.in/dHaHDBS
The UK’s Medicines and Healthcare Products Regulatory Agency (MHRA)
The UK’s Medicines and Healthcare Products Regulatory Agency (MHRA) embeds Global Medical Device Nomenclature (GMDN) in Public Access Registration Database (PARD) for Enhanced Medical Device Regulation. https://lnkd.in/eVGehWFw. In a significant development for medical device regulation, the Global Medical Device Nomenclature (GMDN) has joined forces with…
