Perfectus Biomed have donated to the ‘Buy a Goat’ fundraiser set up by Kathy’s Centre in support of Act4Africa.
Kathy’s Centre is a community health and education facility located in South Eastern Uganda. The centre provides the local...
On 25th May, 2017, the new European Medical Device Regulation (MDR) entered into force, and as a result, existing directives were replaced. The new regulation applies to manufacturers selling medical devices in Europe. It has a transition period of 3 years for...
The World Health Organisation (WHO) have published a list of pathogens which are likely to pose the greatest risk to human health. This is due to their increasing resistance to antibiotics.
The list includes 12 families of bacteria and will be used to promote...
Perfectus Biomed are delighted to announce that we have been shortlisted from over 60 applicants for two awards at the 12th annual High Sheriff’s Awards for Enterprise. The awards are the Mornflake Oats Award for Innovation and also the Cheshire Business Leaders...
The U.S. Food and Drug Administration (FDA) manages the risks that are associated with the use of drugs. They ensure that the benefits exceed the risks by developing a Risk Evaluation and Mitigation Strategy (REMS).
The Current REMS Process