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Good Clinical Practice E6 (R3) Guidance and Implementation
Understanding the Updated ICH GCP E6 (R3) Guidance Good Clinical Practice (GCP) is the internationally recognised standard for designing,...
Why is informed consent crucial in clinical trials?
Just imagine being presented with an opportunity to participate in a clinical trial without knowing the potential side effects, the purpose of the...
How To Become A Clinical Research Project Manager
To become a clinical research project manager, you will need a combination of education, experience, and specific skills. There isn’t one specific...
What makes an excellent training provider?
In today's fast-paced and technologically driven world, online training has emerged as a preferred method of learning for many individuals and...
How do I get a certificate in Good Clinical Practice?
From research conducted around our business area last week, we have found that one of the most common questions typed into Google related to...
Are there really 12 principles in the new GCP E6 R3?
As the revised guideline of 𝐈𝐂𝐇 𝐄𝟔(𝐑𝟑) 𝐆𝐨𝐨𝐝 𝐂𝐥𝐢𝐧𝐢𝐜𝐚𝐥 𝐏𝐫𝐚𝐜𝐭𝐢𝐜𝐞 (GCP) has been endorsed by ICH Expert Working Group (EWG) on 19th May 2023 and the...
Good Clinical Practice – Are you R3 ready?
Introduction: Good Clinical Practice (GCP) guidelines play a vital role in ensuring the ethical conduct and quality of clinical trials. The original...
Medical devices – What’s changed with the new Medical Device Regulations?
So, four years after it entered into force, the Medical Devices Regulation (MDR) is now here. It became applicable on the 26 May 2021. The...
Good Laboratory Practices – Top ten common errors made
Working within a laboratory in a Clinical Trial environment is a complex role. One small action can have major impacts on the outcome of an...