services
Completed Supplier Audits
We conduct the audit and make the report available for purchase. Our Audit Efficiency Program supplier audits can save you 30% or more by leveraging the cost of the auditor’s time and travel expenses. Compare your supplier list to the list below and let us know which ones you would like to purchase. If your supplier is not on the list, or you need a more customized audit, then review the Planned Supplier Audit Efficiency Program supplier audits and let us know which ones you want us to do on your behalf.
Blue Line Sterilization Services
Novato, CA | January, 2024
$2650.00
Nelson Labs - Salt Lake City
Salt Lake City, UT | October, 2023
$2650.00
Infinity Labs - Stone Ave
San Jose, CA | July, 2023
$2650.00
Infinity Labs - Petaluma
Petaluma, CA | May, 2023
$2650.00
Nelson Labs - Itasca
Itasca, IL | January, 2024
$2650.00
Infinity Labs - Tradezone Blvd
San Jose, CA | July, 2023
$2650.00
Steri-Tek
Fremont, CA | June, 2023
$2650.00
What if my supplier is not on the AEP Schedule?
Do you have a supplier that is not on on our list? Maybe you need a more customized audit? Contact us using the form below. We’ll work with the supplier to find other companies and firms looking for supplier audit efficiency so you’re still able to take advantage of the ease and financial flexibility our Supplier Audit Efficiency Program provides.
Contact Sales
Learn More About Our Audit Services
Request Your Audit Services
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.