The Future of Medical Device Regulation
The Future of Medical Device Regulation, on the 16th of September, the Medicines and Healthcare products Regulatory Agency (MHRA) launched a 10- week
The Future of Medical Device Regulation, on the 16th of September, the Medicines and Healthcare products Regulatory Agency (MHRA) launched a 10- week
We still have spaces available on our RPi course running on the 23rd of September starting at 10 am until 12:30 pm.
The last four years for pharmaceutical wholesalers have been tough, uncertain demand and outcomes, bumpy supply chains, uncertain of the changes in regulations ahead, staff shortages have added to the risks already in the business model.
People often tell us that they cannot audit when they come on our course. This is not true they must just look at things differently. They must do their homework to ensure that they know what they are auditing and why.
Deadline approaching – Medical Device Registration for registering Class IIa and Class IIb (other than implants) products with the MHRA is the end of August 2021.