Clinical Trial Operations

In a time where CROs and Sponsors continue to face increasing challenges in the recruitment and delivery of clinical trial results, you can be assured that TDDA is a trusted partner in global clinical research. Our capabilities include:


Study feasibility and site capability assessments

Protocol design consultations

Growing network of satellite sites

Central budget negotiations

Full clinical protocol execution

Patient Recruitment and Retention

TDDA has demonstrated a proven track record when it comes to achieving recruitment and retention targets, often recognized as the highest enroller or first launched Canadian site. Our success is largely attributed to our unique internal recruitment model built on a network of research-oriented physicians and sites, experienced in the conduct of clinical trials, assessing treatment pathways and identifying patient candidates for whom a clinical trial may provide added treatment options. Because our physicians and clinical teams are able to offer a continuing care model, patients do not experience disruptions in their overall care, resulting in high retention rates for our
clinical trials.

Site Management

As TDDA continues to grow as an organization, we are able to offer our industry partners greater access
to physicians and clinical trial sites across Canada, effectively increasing our capabilities through one centrally managed group.

TDDA will provide centrally managed services related to business growth and trial start-up,
allowing you and your coordinators, to focus on conducting clinical trial procedures and patient care.


Centralized Services
Business Development | Start-up Contracts | Financial Services Regulatory | Central Ethics | Clinical Operations Support | Standard Operating Procedures | Training | Site Integration & Support


Site Level
Execute Study Procedures as per protocol/SOPs | Complete Source and eCRFs | Support On-Site Monitoring Visits | Maintain Facility, Investigational Drug and Equipment