Quality Management Systems for Medtech

Cannon Quality Group’s team of engineers are experts in the quality management field—they have the experience to grasp your project’s details immediately.

Allow us to help your company’s next Medtech project.

What we Do

Cannon Quality Group

Quality Management Services

Welcome to Cannon Quality Group! Since 2010, we have been providing Quality Management Systems (QMS) solutions to medical device, Medtech, IVD, and pharmaceutical companies of all sizes and stages in their product development lifecycle. We have worked on QMS services with software-as-a-medical-device (SaMD) organizations. Our number one priority is delivering QMS solutions that make sense for the stage and goals of your business. Cannon Quality Group implements this focus by following two core beliefs: We don’t believe in fear-based Quality. We don’t believe in a one-size-fits-all Quality Management System.

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Audit Services

We offer both internal and supplier audits to help you improve your quality system to meet regulatory requirements and make you aware of your supplier’s quality system capabilities.

Events

Connect with CQG at:

  • LSI USA 24
    March 18
  • AI in Medical Imaging
    March 28
  • 2024 UCSF Rosenman Symposium
    May 21
  • Rosenman Innovators Demo Day
    June 12

Upcoming Planned Supplier Audits

  • Steritek, June 2024
  • Nelson Labs (SLC), October 2024

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Completed Audit Reports

  • Blue Line Sterilization Services, January 2024
  • Nelson Labs (Itasca), January 2024
  • Nelson Labs (SLC), Oct 2023
  • Infinity Labs (Stone Ave), July 2023
  • Infinity Labs (Tradezone), July 2023
  • SteriTek, June 2023
  • Infinity Labs (Petaluma), May 2023

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Quality services

Our Services

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Device Compliance Essentials for Startups

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FDA QSR Compliance for Medical Devices

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First in Human

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Food & Drug Branch (FDB) Certification & Audits

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Internal Audits/Supplier Audits

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Medical Device QMS Implementation, Simplification & Compliance

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Outsourced Medical Device Quality Control

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QMS Services to Earn Your ISO 13485:2016 Certification

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Quality Projects

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Quality System Training

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Simplify & Restart Your Quality Management System

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

(925) 232-1003‬

Cannon Quality Group, LLC
77 Front Street
Danville, CA 94526

Writing Templates

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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

 

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