services
Medical Writing Services
Unlock the Power of Expert Regulatory and Clinical Documentation
Welcome to Cannon Quality Group, where 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 team can support your journey regardless of stage. Whether you’re in pursuit to obtain the CE mark or seeking qualified medical writers to meet reporting deadlines, we have the infrastructure in place to help our clients meet their commercial objectives.
Why Choose Us:
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.
What We Do:
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
Ready-to-use QSI Templates
Are there certain documents you need to move your system forward?
Download the Alio Case Study now to discover how CQG helped Alio stay organized and on track through every step of their journey.
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.
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