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FILTER ALL BLOG POSTS Browse By Topic Ideation & Prototyping Establishing a QMS Product Development Regulatory Submission Post-Market Surveillance MedTech Lifecycle Excellence MedTech Lifecycle Excellence HTEC GROUP PARTNERS WITH GREENLIGHT GURU TO ACCELERATE TIME-TO-MARKET FOR MEDICAL DEVICE COMPANIES Greenlight Guru April 27, 2023 Expanded partnership will galvanize MedTech companies’ push to improve the quality of life. Read More MedTech Lifecycle Excellence AVOIDING POTENTIAL ISSUES WITH YOUR 510(K) SUBMISSION Etienne Nichols April 27, 2023 When bringing a medical device to the market, it’s important to be aware of the fatal 510(k) flaw. In today’s episode, Mike Drues joins the podcast to discuss the... Read More Product Development 4 ADVANTAGES OF AN EQMS OVER A PAPER-BASED QMS Etienne Nichols April 21, 2023 One of the biggest factors that determines a medical device company’s success is how effectively they manage quality processes. 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Read More Product Development 4 REASONS TO STOP MIXING YOUR CLINICAL DATA COLLECTION METHODS Páll Jóhannesson April 17, 2023 They say that variety is the spice of life—but when it comes to blending clinical data collection tools, it’s more like dumping the whole spice rack in the pot. One of the... Read More Establishing a QMS HOW TO AVOID A FAILED QMS IMPLEMENTATION Taylor Brown April 16, 2023 No one implements a new QMS just for fun. Read More MedTech Lifecycle Excellence WHY BUILDING SUPPLIER RELATIONSHIPS IS SO IMPORTANT Etienne Nichols April 12, 2023 How do human relationships impact supplier management in the medical device field? Today you’ll hear from Taylor Brown, a Medical Device Guru and Manager of Onboarding... Read More 1 2 3 4 5 6 7 8 9 * * 1 * 2 * 3 * 4 * 5 * Next EXPERIENCE THE GURU EDGE OUR INDUSTRY EXPERTISE EXTENDS BEYOND OUR SOFTWARE. EXPLORE OUR OTHER RESOURCES THAT ARE HELPING LEADING MEDTECH COMPANIES REACH SUCCESS. 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