DocQc is a clinical trial consultancy that supports clinical research through the provision of trial monitoring, site management & GCP auditing services for both medical device and pharmaceutical studies: pre-market to post-market.

Since 2015, we have been supporting Sites and Sponsors in all aspects of planning and conducting clinical trials in accordance with federal and local regulations.

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Areas of expertise include but are not limited to:

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• Anesthesiology

• Cardiovascular System

• Infectious Disease

• Neurology

• Oncology

• Ophthalmology

• Natural Health Products

• Gene Therapy

• Vaccines

A Clinical Trial Team You Can Trust

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Our experience and approachability make DocQc the perfect partner for clients with different types of needs. Our team is well versed in ICH GCP, ISO14155, FDA and Health Canada regulations. We have a proven track record of high quality work and leadership in clinical trial management.

DocQc has vast experience in Abuse Liability, Alcohol Interaction, Bioavailability/Bioequivalence, Drug –Drug Interaction, Dose Selection and First-In-Human clinical trials from start up to closeout; not to mention medical device trials.

Our team members have participated in many study audits and regulatory inspections receiving ratings of compliance and/or good standing. Feel free to contact our team for any questions. We are excited to guide you through the process.