As one of the most experienced and leading CROs (Contract Research Organization) for over 35 years, McDougall delivers valuable insight to biotech and pharmaceutical clients across all phases of their clinical trials. With timely, accurate data and analytics, we help clients expedite their time-to-market and lower development costs.
McDougall Scientific specializes in Clinical Trial Design services, Statistical Analysis and Clinical Data Management. Known for delivering insights you can trust, we take the time necessary to understand your business requirements, align with your regulatory strategy, and mitigate risks to deliver a vital statistical strategy for the development of your product.
The result: a smooth, efficient, and trusted operation from start to finish. We welcome you to contact us whether you are a company with established assets, or an independent investigator exploring initiating an investigator trial.
Feasibility Assessment, Protocol Development, Study Startup, Project Management, Investigator Initiated Trials, Phase I-IV Trials, Clinical Data Management System, Statistical Services, EDC, Data Management, Supply Management, Randomization, Document Management, Clinical Trial Management, Site Monitoring, Medical Writing, Regulatory Services, Pharmacokinetics, Patient Recruitment, Pharmacovigilance, Safety Surveillance, Integrated Safety, Risk-based monitoring