The new EU GMP Annex 21 came into force in August 2022 and is intended to summarize all EU GMP requirements applicable when importing medicinal products from outside the EU/EEA. If your company is importing… Read More »Importing Medicines into the EU

As consumers, we are increasingly tempted to turn to online sources for medicines nowadays due to our changing shopping patterns and as a side effect of the recent pandemic. But, unfortunately, there are always those… Read More »The illegal supply chain, counterfeiting and the Falsified Medicines Directive

Are you looking to dip your toe into contract QP work and get in at the beginning with new start-ups? Do you want to work just 2-5 days per week with a small number of… Read More »Orion GXP Consulting are hiring a Consultant QP!

The old Clinical trials directive 2001/20/EC was seen as bureaucratic and had many obstacles, such as not having a streamlined mechanism for authorising sponsorship of multi-centre studies to be carried out across the union. There… Read More »Now that it has gone live, is the new Clinical Trials Regulation revolutionary?

GMP regulations require that all manufacturing processes must be documented and can be traced from beginning to end.  Complying with GMP guidelines makes sure that companies produce high-quality medicinal products for patients and ensures that… Read More »Why is good manufacturing practice so important in the Pharmaceutical industry?

Since our last post in February, things have been really busy with Orion Consulting. We have been busy building our new website and professional network, managing new contracts and making plans for the future. An… Read More »Guest lecture at ATU and new website!