SOPs play a crucial role in clinical quality assurance and it is therefore essential that they are understood and followed by all end-users in a clinical trial. If SOPs are not followed correctly, the validity of data generated is compromised, leading to warning letters being issued and delays in the trial process. Auditors and inspectors see SOPs as essential and following them is crucial.
In this highly interactive course you will develop the skills and practical experience required to write and review SOPs for GCP compliance. Participants will review GCP fundamentals and also relevant regulations. This knowledge will then be used to examine considerations of style, length and content.

Registration required:

Yes

Free:

No