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.
Clinical Trial Monitoring & Site Management
Clinical trials mark a costly phase in the development process due to delays and/or interruptions. Let DocQc oversee the conduct of your clinical trial.
Quality Assurance Auditing
DocQc possesses considerable experience in GCP auditing of clinical trials and assessing their compliance with different regulations.
Medical Monitoring
DocQc provides rigorous oversight and valuable medical insight to clinical trials, from study design to close-out.
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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.