Quality Assurance Audit

Clinical Trial Services

DocQc assess all the elements of your clinical trial to ensure that the study adheres to the clinical objectives, upholding ethics and data integrity. Our team assesses the scientific qualifications of the project team members, provides them with GCP training, reviews documentation and reporting structure and participates in site selection. We also conduct phase-specific GCP audits.

DocQc possesses considerable experience in GCP auditing of clinical trials and assessing their compliance with different regulations. With the ever-changing landscape of clinical research, your team needs experts who keep themselves well informed of the changes occurring in our continuously developing digital age.

Through our audits, we improve your management of trial products, informed consent and participant safety.

We are involved in amending inadequate protocols, establishing deviation procedures, improving data and records management, setting guidelines for AE/SAE reporting, and more.

DocQc inspects site facilities and equipment as well as user access and controls for computer systems, ensuring the site is prepared for regulatory inspection. We don’t compromise on compliance or quality and you shouldn’t have to. DocQc will listen to your concerns and customize an audit plan to meet your needs.

Prepare your team and trial for regulatory inspections. Contact DocQc today for effective quality assurance auditing.

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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.