
Be Careful What You Advertise
Most of us will know that it is illegal to promote prescription only medicines (POMs) to members of the public, however, it is always worth a reminder that you must be careful what you advertise.
Most of us will know that it is illegal to promote prescription only medicines (POMs) to members of the public, however, it is always worth a reminder that you must be careful what you advertise.
In good news for the UK Health economy, the Government last week published a draft policy to allow medical devices and IVDs that have been approved in certain other countries quicker access to the UK market.
Self-Inspections are an important part of GDP and ensuring you keep your activities and licence compliant.
Those companies manufacturing and handling medical devices should be aware that there are changes to the UK regulatory environment coming.
When operating a pharmacy, the General Pharmaceutical Council (GPhC) will come and inspect you against the pharmacy standards, do you know what evidence you will need to present to demonstrate how your pharmacy adheres to the standards?
The MHRA have made the first release of their RegulatoryConnect service available which allows tracking of the submission status of product licence applications but will soon offer much more.
The Medicines and Healthcare products Regulatory Agency (MHRA) announced that from the 31st of January 2024 new regulatory measures have been implemented to ensure that the known harms associated with valproate use are reduced.
A press release from the MHRA today, 20th February 2024, has announced that Codeine linctus will be reclassified as a prescription only medicine because of the risk of abuse and addiction.
Pharmacy First officially launched on 1st February 2024 and 95% of pharmacies in England have signed up for the service. Pharmacists will soon have referrals from surgeries and from other sources for patients with sinusitis, sore throat, impetigo, UTIs, earache in Children, shingles and infected insect bites; and will be able to supply antibiotics where indicated.
The MHRA is the first Regulatory body in the world to authorise a Crispr-based gene therapy.