Training

We provide GCP training for our Clients’ clinical staff located in Russia and Ukraine.

The courses can be set at different levels to meet Clients’ needs, from the ICH GCP basic principles and regulations through to more practical-based training with workshops and learning outcomes. Course folders and a certificate of attendance are included as part of the package.

Please find selected training topics, which can be delivered to our Clients’ staff:

• Patient information and consent
• Investigator’s site monitor
• Study-specific monitoring activity, Types of the site visits
• Essential documents for the conduct of a Clinical Trial
• Source Documentation within Clinical Trial
• Handling Investigational Product
• Regulatory Requirements for Clinical Trials Conduct in Russia

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