COLTRIALS develops the role of advisor from the beginning of the clinical trial, providing our clients with knowledge and experience to help them achieve the objectives established within the regulatory scope in clinical research.
literature review, design, protocol and annexes writing, statistical analysis, design, validation, CRF manual and surveys, information quality review, informed consent database cleaning, review of new versions of consents/assents or additional protocol versions.
The initial documentation and provide advice and consultancy for the start of the clinical trial or study.
throughout the development of the clinical trial.