We provide monitoring of the clinical study in accordance with the protocol, legislation and Good Clinical Practice - comprehensive and partial services:

• Creation of documentation (monitoring plan) and cooperation in the development of the study protocol and other relevant documents for the implementation of the study.
• Ensuring the implementation of the clinical study in the implementation centres - opening and activation of the centre, monitoring visits and closure of the centre including reporting
• Regular communication with study teams and the project team
• Overseeing protocol compliance, study progress and data collection, including checking the accuracy and completeness of data entered on the data collection form
• Ensuring quality and safety during the conduct of the clin