Depending on the scope of your project, our experts will work with you to establish a timeline and budget. Budget will be dependent on the number of services and staff members involved in the project, the complexity of the task, and the length of the trial.

We can also provide consulting services for the submission of your research project to SR&ED Tax Incentive Program.

CCCT experienced medical research experts design individualized clinical trial protocols optimized to meet study outcomes. All protocols are written in abidance with the Good Clinical Practice (GCP) Guidelines. At CCCT we create all necessary source documents for accurate data capture as outlined in the protocol:

• Informed Consent Forms (ICFs)
• Case Report Forms (CRFs)
• Assessment Schedules
• Investigator Brochures

CCCT has expertise in submitting regulatory applications for clinical trials, ensuring compliance to Institutional and Independent Review Boards (IRBs) and Health Canada requirements. Our staff will manage regulatory submissions and correspondence with the regulatory board (s) on your behalf to acquire study/product approvals.

Our Research Team is composed of qualified investigators and study coordinators that will aid clients with the process of study conduction and data collection at either client’s site or at the Canadian Centre for Clinical Trials. Canadian Centre for Clinical Trials is a clinical research site with more than 10 years of experience conducting Phase II-IV trials for well-known pharmaceutical organizations. Our site has designated space for patient visits, procedures, sample processing and study document archiving. Our research facilities are in accordance with GCP standards. We have a proven track record of successful completion of all trials, and a high retention rate of study participants.

CCCT offers a range of services that can be customized to meet each client’s project needs and provide quality assurance. Our service includes:

• Site and Investigator(s) recruitment
• Site start-up
• Coordinating project sites to ensure compliance with protocols
• Creation of Standard Operating Procedures (SOPs) for uniform performance across selected sites

At CCCT we provide customizable solutions for clinical trial data management. Our clients can be assured that efficient and effective data collection and management underlie the services we offer to best serve the needs of each project. Our services include:

• Database design and maintenance
• Data validation and cleaning
• Data processing and quality control
• Integration of third-party data

CCCT medical research experts will design an analytical approach to investigate collected data in accordance with the nature of the study objectives, ensuring appropriate reporting of clinical trial outcomes. Clients can expect prompt services that will expedite study completion and eliminate the need for corrections while maintaining quality and accuracy. Our expertise includes:

• Sample size and power calculations
• Statistical Analyses Plan (SAP) development
• Randomization schedule generation
• Interim assessment for rational decision making
• Statistical analysis in accordance with current methodologies
• Customized interpretation of data for study reports

CCCT medical writers offer a broad range of expertise making them suitable for regulatory and technical writing in a variety of therapeutic fields. We will partner with you to eloquently compose:

• clinical study reports
• research articles for journal submissions
• abstracts, presentations, and posters for conferences and scientific meetings