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ICH GCP E6(R3) Training for Your Company
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Your Name
Your email address and phone number
Your company
Your position
When would you like us to run a GCP R3 training for your employees?
How many learners will be there?
What are their roles in Clinical Trials?
Investigator Site - Physician (PI / SI)
Investigator Site - Pharmacist
Investigator Site - Study Nurse
Investigator Site - Study Coordinator
Investigator Site - Other
IEC / IRB member
Sponsor / CRO - Monitor / CRA
Sponsor / CRO - Central Monitor / CMA
Sponsor / CRO - Other
Vendor / Non-CRO - Project Manager
Vendor / Non-CRO - Other
Other
How many newcomers in GCP will be in the training?
None, all people have some experience
<25%
Closer to a half
75%, or almost all are new in Clinical Trials
If the language of the training is different from English, please, name the preferred language of the training
What training delivery method would you like?
Face to face in the classroom (address or city below)
Live online (Zoom, MS Teams, etc.)
Self-paced e-learning available at any time and on any device (mobile, PC, tablet)
Combined
If you chose the classroom option please specify the location
What is the goal of this CGP R3 training?
Briefly discuss the difference between R2 and R3
Teach GCP basics with the focus on R3
Teach GCP + real cases to be prepared for real-life situations and audits
How many hours can you dedicate to this training?
Is there anything else you would like us to take into consideration?
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