Training

Our training programs are a combination of lectures and workshops. Training courses span beginning to advanced levels of knowledge. Detailed course materials are provided to participants along with certificate of participation. Courses are specifically designed to meet client needs in the areas of:

• ICH GCP E6(R2) Addendum (and upcoming Revision 3, expected in 2023)
• Good Laboratory Practice (GLP)
• Good Pharmacovigilance Practice (GVP)
• Good Manufacturing Practice (GMP)
• Inspection Readiness
• CSV / 21 CFR Part 11

On 25-Jan-2025, the EU Clinical Trials Regulation (CTR; No. 536/2014) will officially replace the EU Clinical Trials Directive (CTD; 2001/20/EC) at the end of a transition period.

Our team of professionals offers targeted training to help you prepare for the new system of conducting clinical trials in the EU.

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