Cannon Quality Group

06/19/2024

Medical device manufacturers! Get ahead in the compliance game with our exclusive, free GSPR Template from Greenlight Guru and CQG. Originally $349, this tool helps you quickly assess compliance, pinpoint nonconformities, and ensure MDR adherence. Protect your organization and prioritize patient safety—download today: https://hubs.ly/Q02CmsZ40

A free, comprehensive template to help medical device companies streamline the General Safety and Performance Requirement (GSPR) process for MDR compliance.

06/18/2024

"CQG’s impressive flexibility kept multiple projects on target, assisting us with a variety of projects from non-product software validation to EU MDR implementation and support. With Cannon’s help, we were able to prepare for EU MDR and Kingdom of Saudi Arabia (KSA) Medical Device submissions. CQG also performed literature review and compiled our GSPRs prior to submission. CQG proved to be an invaluable partner in keeping us organized and on track." -Roop Pandher, Director of Quality, Alio.

Download the case study today: https://hubs.ly/Q02Cmtp_0

06/14/2024

We are honored to be listed as one of the top 2024 medical device consulting firms by Qualio . https://hubs.la/Q02BX1RZ0

We've hunted the top medical device consulting firms for 2024. Dive into the expert teams that can lift your medical device company to the next level.

06/14/2024

Explore Option 2/3 of our new Compliance Program: Individual Expert Meetings! Get personalized, bi-monthly 60-minute meetings with a Quality/Regulatory Assurance Expert. You'll receive a proprietary QS Dashboard Template and have access to purchase procedure templates as needed. Tailor this support to fit your startup's unique needs. Learn more and see if this is right for you: https://hubs.la/Q02BWXDc0

06/12/2024

CQG is attending Wilson Sonsini’s 31st Annual Medical Device Digital Health Conference. We look forward to diving into critical topics like healthcare regulations, IP valuation, fundraising trends, and partnering strategies. Joining industry leaders for networking and presentations. More info: https://hubs.la/Q02ByHc90

06/12/2024

Nicolle Cannon is attending the MedTech Innovator Summit today! featuring the top early and mid-stage start-ups in the medical device industry. The annual Summit is a lively and engaging event that exclusively allows the leadership teams from our latest cohort of startups to get to know each other and exchange ideas with MedTech Innovator’s partners, alumni, and other industry leaders. https://hubs.la/Q02ByQVB0

06/12/2024

You are invited to an exclusive networking event with MedtechWomen on Tuesday, June 25, 2024, from 6:30-8:30 PM in beautiful Danville, CA! Hosted by Nicolle Cannon and Lindy Vejar, this event is your chance to connect with inspiring female leaders in medtech and engage in meaningful discussions in a fun, supportive environment. Don't miss out—there are only a few spots left, so pre-register today to secure your place! Register Here: https://hubs.la/Q02Byzfz0

06/07/2024

Looking for tailored solutions to streamline compliance in your industry? Our QSI templates are now available on our website. Our ready-to-use quality system implementation templates ensure seamless compliance, empowering your organization with simplicity and efficiency. Visit our website now to discover how our QSI templates can revolutionize your quality management processes: https://hubs.la/Q02zw6nX0

Our QMS templates are precisely tailored to meet your needs. These documents ensure compliance, empowering your organization with simplicity and efficiency.

06/06/2024

Our Steritek audit is coming up this month - have you signed up to receive the report? Our streamlined approach conducts a single audit on behalf of multiple companies, maximizing efficiency without compromising quality. Explore our full schedule, access completed reports, and pre-order upcoming audit reports now: https://hubs.ly/Q02zwtLV0

06/05/2024

For medical device manufacturers, each new market potentially entails a complex web of fresh and varied regulatory frameworks. As this complexity mounts, the costs and burdens of compliance can become overwhelming. Download our latest white paper: "ISO 13485 to QMSR: Pathway to Success - What You Need to Know" on our website: https://hubs.ly/Q02zwpy70

06/04/2024

We can't wait to attend the MedTech Innovator Summit on June 12, featuring the top 80 early and mid-stage start-ups in the medical device industry. Can witness their innovative ideas and game-changing technologies. https://hubs.ly/Q02zwwrg0

06/04/2024

The journey of bringing a medical device to market can often be sidetracked by unforeseen challenges, which underscores the importance of meticulous planning and adaptability. Our recent experience with a FDA PMA audit sheds some light on the complexities in navigating the FDA submission process: https://hubs.ly/Q02zwjq-0

Exploring insights from an FDA audit pause during PMA submission process.

05/31/2024

Cheers to three years of groundbreaking ideas and visionary leadership with Jeff Flint, our Director of Innovation! Your passion for pushing boundaries and driving progress inspires us all. Here's to many more years of innovation and success together!

05/31/2024

We are looking forward to the 2024 Rosenman Innovators Demo Day on June 6. We are proud to be partners with the Rosenman Institute, where we engage with Rosenman entrepreneurs to build lasting, win-win business relationships with fast-growing healthtech companies.

05/30/2024

Introducing Option 1/3 of our new Compliance Program: the Start-up Cohort! Join bi-monthly, 60-minute group meetings with a Quality/Regulatory Assurance Expert and discuss your issues with a small group of peers. This option is perfect for startups looking to share experiences and gain insights. Limited to 10 companies, apply by June 14th! Learn more here: https://hubs.la/Q02yX8RQ0

05/30/2024

Are you setting the stage for compliance early enough? Cannon Quality Group is excited to offer a cost-effective program tailored for early-stage MedTech, Pharmaceuticals, IVD, or SaMD/SiMD startups. Our program addresses key FDA and EU/MDR ISO 13485 requirements to help you set up a QMS with minimal effort and cost. Perfect for those needing Quality and Regulatory Support! Learn more and see if you're a fit: https://hubs.la/Q02yX8RL0

05/30/2024

Ensure your medical device meets EU MDR requirements with our FREE GSPR Template (reg. price $349), courtesy of Greenlight Guru and CQG! This comprehensive 80-page guide helps you evaluate compliance, identify gaps, and streamline your documentation process. Download now and expedite your Notified Body accreditation! Download Here: https://hubs.la/Q02y-0--0

A free, comprehensive template to help medical device companies streamline the General Safety and Performance Requirement (GSPR) process for MDR compliance.

05/28/2024

At CQG, excellence meets innovation in our new Certified Medical Writing Services. As a trailblazing quality management systems company, we're expanding our reach to cater to your medtech needs with precision and insight. Our certified medical writers possess unparalleled knowledge of the complex medtech landscape. Their mastery of regulatory requirements and clinical protocols ensures meticulous precision. Learn more: https://hubs.la/Q02yHqxP0.

Industry-Leading Expertise: Our certified medical writers possess detailed knowledge of the complex MedTech landscape. Their mastery of regulatory requirements and clinical expertise ensures the latest state-of-the-art assessments and EU MDR compliance.