about us
Testimonials
CQG was given a task to plan, execute, and report on 4 separate Computer System Validations under an aggressive timeline while an IT buildout was being implemented at our site. CQG was extremely collaborative with the IT provider and very transparent with Sword Bio on all areas of the process. The project was completed on-time and under budget. I would like to thank Mike, Josh, and Kareem for their dedication to this project. I was more than happy with the results and look forward to utilizing CQG for other service options.
I am working on aging and packaging which they specifically said was assigned based on my experience at Cannon. Your internship program is literally the gift that keeps on giving.
Just wanted to drop a quick note to thank you all for your support over these past several months. We had a very successful audit this week. Both auditors were very complimentary of the progress we have made since the last audit and that is really a testament to the work you have all done on our behalf. The Change Orders were clean, the CAPAs were impeccable, the internal audit report was very robust and served as the backbone to much of the audit. We are now in a much better position with our notified body. Again, thank you.
Look what you have done! Profusa has a functional QS thanks in large part to you. The GMED auditor has conducted over 700 audits and said we have an extremely good QS and a lot of that credit goes to you… I just wanted to let you know that Profusa couldn’t have done it without you and it is much appreciated.
It was by far the best QSR/GMP training – high caliber content and engaging delivery.
My Manager reviewed and approved this validation, and he called me to say it would be the gold standard for spreadsheet validations for all Nordson Medical D&D sites from this point forward!
Your team is great, love the maturity level. Great respect from Quality & Regulatory.
For our startup, CQG made QSR development and compliance enjoyable and easy. Their unique style and system has allowed us to work at the fast pace required by the market, while still maintaining regulatory compliance.
I found everyone I worked with at Cannon to be professional and a pleasure to work with. They have excellent tracking systems in place to assure tasks are not forgotten.
Cannon Quality Group (CQG) was founded in 2010 as a full-service outsourced quality management company serving the medical device, Medtech, pharma, IVDR, SaMD, and general life science community with right-sized quality management system solutions.
Contact
Cannon Quality Group, LLC
77 Front Street
Danville, CA 94526
Writing Templates
Streamline Your Medical Writing Efforts Today!
Unlock Efficiency and Precision with Our Comprehensive Medical Writing Templates
Available Templates
Clinical Evaluation Protocol & Report
Accurately document your clinical trial evaluations with our meticulously crafted Clinical Evaluation Protocol & Report Template, ensuring adherence to regulatory standards and efficient data reporting. Streamline your review process, from protocol to comprehensive reporting, with our user-friendly template, designed to clearly outline the clinical evaluation review process.
Literature Search Data forms
Elevate your literature search review process with our Literature Search Data Form, which offers a structured approach to identify and document relevant studies, guiding you in extracting and synthesizing key information. The data search form empowers you to conduct comprehensive reviews with efficiency and precision, ensuring a robust foundation for your literature review report.
Literature Search Protocol & Report template
Take advantage of our Literature Search Protocol & Report Template. This comprehensive tool provides a systematic framework for designing and executing a meticulous literature search, ensuring adherence to best practices. Seamlessly transition from defining search strategies to synthesizing findings, empowering your research with a structured and efficient approach that aligns with the highest standards of excellence.
Data Extraction form
Utilize the data extraction form as a tool to record pertinent information from studies identified in your literature search.This form ensures a systematic and organized approach to extracting key data from the literature search process, ultimately accelerating your data synthesis and analysis.
Declaration of Interest (DOI) form
Leverage the Declaration of Interest (DOI) form to ensure compliance with EU Regulation (EU) No. 536/2014 on Clinical Trials.
Notes: Post market surveillance, PMS, periodic safety review, PSUR, Clinical investigation, CEP, CER, literature, safety and performance, state of the art, MDR, IVDR, MEDDEV, clinical
TBD Testimonial to go here.