MED Institute supports consultants, manufacturers, and developers of medical products through the key phases between the start of an idea and making a product available to clinicians and patients. With more than 40 years of experience in medical device testing, engineering, data analysis, global regulatory submission preparation, and clinical trials, our team knows what it takes to guide a product through all the complex steps required for market approval. Contact us today to learn how we can partner with you medinstitute.com | 855.463.1633.
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If you missed our tech talk presented by Dan Dillon, MS, RAC at MEDevice Boston last week, please get in touch with us to learn more about the top 10 rules for successful FDA submissions. https://lnkd.in/g8YEiast
One of the best presentations that I have seen this year. Top 10 Rules for Successful [FDA] Submission from Dan Dillon, MS, RAC at MED Institute MEDevice Boston #medicaldevices
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Had the opportunity to attend the Regulatory Affairs Professionals Society (RAPS) convergence last week to learn more about the state of medical device regulation in the world!
If you are attending MEDevice Boston this week, stop by booth #946 to meet our team members Samantha Stevenson, CST/CSFA, CCRP and Dan Dillon, MS, RAC! Don't miss our tech talk tomorrow at 11:30am in the tech theatre. Dan Dillon, MS, RAC will present the Top 10 Regulatory Rules for Successful Submissions. #MEDeviceBoston2024
If you are attending NASS this week, connect with Abby Anttila! She will be networking onsite today and tomorrow! #NASS
Do you have a medical product that you would like to bring to market? We can help you you determine your regulatory path to approval. Reach out to us today to discuss your project needs. https://lnkd.in/gN6MCnPs #Regulatory #productdevelopment
Catch Abby Anttila and Amy Kester at AAOMS walking the exhibit hall and sharing MED Institute’s services!
CEC meetings provide a sounding board for experts in the field of the investigational product to determine if an adverse event is related to the clinical intervention. These gatherings allow the potential to spot unanticipated adverse events linked to treatments, ultimately providing another level of safety to patients. Altogether, a CEC is another valuable tool available to ensure the safety and welfare of patients participating in clinical research. https://lnkd.in/gFgUA2yf
Visit us in booth #946 at MeDevice Boston September 25 - 26! Samantha Stevenson, CST/CSFA, CCRP and Dan Dillon will be onsite to answer any questions you may have. Don't miss our tech talk! Dan Dillon will present the Top 10 Regulatory Rules for Successful Submissions on September 26th at 11:30am in the tech theatre. #MEDeviceBoston2024 https://lnkd.in/gp4Vgjpx
For medical devices, ensuring safety and efficacy doesn’t stop once a product hits the market. Post-market clinical follow-up is a crucial phase in the medical device lifecycle, designed to monitor performance and safety in real-world settings. https://hubs.ly/Q02NR5BS0