Cannon Quality Group
News & Updates
Navigating MedTech Excellence: Insights from GLG’s True Quality Summit on Proactive Compliance and Digital Solutions
Greenlight Guru, CQG, and other industry leaders discusses proactive compliance, digital solutions, and innovation for impactful devices.
FDA’s Draft Guidance on Fee Waivers for Struggling Small Medical Device Businesses
FDA’s proposed fee waivers offer relief for for struggling small medical device businesses.
Success at MD&M West: A Glimpse into the Future of MedTech
CQG connects at MD&M West, forging relationships, embracing innovation, and driving growth in MedTech.
EU to U.S. Market: Understanding 3 Core Regulatory Contrasts
There are important differences in medical device compliance for both the European Union (EU) and U.S. markets. Understanding these three core regulatory contrasts can make the difference in the success of your market entry. Check out this MasterControl article by our very own Technical Writer Becky Blankenship on the subject.
Analyzing the Top 4 Trends in 2023 Medical Device Recalls
Keeping track of current trends in FDA medical device recalls is an integral aspect of risk management and staying informed about the FDA's current line of thinking. This is especially vital for MedTech startups lacking regulatory experience, as tracking recall trends...
Three Key Considerations When Going Paperless
Ditch paper in MedTech! Learn how with expert guidance from CQG and Qualio.
Securing Investment: Insights and Tactics
Learn how to secure life sciences investment as CQG & Qualio share startup funding tips and insights from their latest webinar.
MedTech Women Vision Focuses on Healthcare Equity
Leaders in MedTech unite to address disparities in healthcare at the MedTech Vision 2023 annual conference.
Navigating eQMS today with Qualio
Enjoy highlights from CQG’s most recent eQMS webinar featuring eQMS provider Qualio. Gain insight into how choosing the right eQMS system can empower your startup and streamline compliance, allowing your business to evolve successfully.
Unlocking Success in MedTech: Insights from DeviceTalks Boston
Cannon Quality Group joined industry leaders at DeviceTalks Boston 2023, highlighting sustainable innovation and practical insights for MedTech start-ups.
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Quality Management 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
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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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