Remote Auditing versus On Site Auditing
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.
Risk Assessments – Evaluating hazards
Risk Assessments: The aim of writing one is to evaluate hazards, then remove that hazard or minimise the level of its risk by adding control measures, as necessary.
WDA(H) & Import – New Guidelines:
Following Brexit and GB leaving the EU the MHRA have advised that GB wholesale dealers now need to appoint an RPi
API registration
API registration is an MHRA requirement if you manufacture, import or distribute active substances and you are based in the UK.
New Contract RP introduction
New Contract RP says hello! Please allow me to introduce myself as the newest member of PCL’s Contract RP Team.
Export & WDA(H) – Updated Guidelines:
As Great Britain (GB) are no longer part of the European Union (EU) since the 1st of January 2021 exit date. It is essential to ensure all the necessary changes have been made to remain MHRA compliant.
Refrigerated Medicinal Products – what to consider…
How do you manage YOUR refrigerated medicinal products? Check out 10 key points to ensure you are shipping your products effectively
Toll Manufacturing or Contract Manufacturing which one should you choose?
It is difficult to determine which process is better of the two- Toll Manufacturing or Contract Manufacturing.
What is a Stringent Regulatory Authority?
“Stringent Regulatory Authority or SRA” is a term that was developed by the WHO Secretariat and the Global Fund to Fight AIDS, Tuberculosis and Malaria.
