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.
In all the noise over the past year regarding Covid 19, children have been affected the most, they may have been the least affected by the virus itself but they have suffered disproportionately from lockdown.
What have we learned in ten years? I was a pharmacist in retail practice in 2009 and was a site that collected all the unused Tamiflu which ended up being destroyed having cost billions across the world.
The number of digital consultations has exploded during the pandemic and for some it has been fantastic, but for other is in not a suitable mode of to name a few; elderly who are not silver surfers and autistic children.
Remote Auditing versus On Site Auditing: For the last 16 months the pharmaceutical world has had to get used to remote auditing as opposed to auditing in person.
