If you are interested in your professional development and you should be then read on. Read more…
As you can see from our website if you take our Introduction to GCP course you are entitled to CPD points from ICR and the faculty of Pharmaceutical Medicine.
The table below shows a snapsot of available courses to help you to make an informed decision about which provider to choose. Read more…
Before GCP each country set it’s own satndards and the only source of guidance was from FDA. Read more…
GCP is important because it underpins the European Directive and clinical trial legislation in EU and other countries. Moreover, it is now much more widely adopted in countries in addition to the EU, USA and Japan and is now almost universally recognised as the standard for doing clinical research. Another aspect of GCP is to provide standardised guidance for quality standards and the content and structure of regulatory submission dossiers.
However, do not think that a good working knowledge of GCP iss all you need. Although local clinical trial legislation is largely based on GCP there are often differences that you need to be aware of. Being in breach of GCP is bad but breaking the law has much more far-reaching consequences. Do you where UK clinical trials legislation differs from GCP??? Read more…
We are all looking for ways to cut costs. favourite areas are usually travel and training. Cutting costs on training may have short-term benefits but could lead to major long-term problems. Read more…
Training is one of the first things to go when money gets tight but everything has a price!
If you are involved in manufacturing or sponsoring/ conducting research into medical devices you need to be fully aware of the new standards defined by the latest version of ISO 14155 ( Clinical Investigation of Medical Devices in Human Subjects)
Check out our brand new, unique, e-learning module on ISO 14155 and get ahead of the game now by using our innovative approach to learning.
