COMAR, a renowned name in the medical devices and packaging solutions industry, has achieved a significant milestone by successfully obtaining their CE certificate under the latest EU Medical Device Regulations (EU MDR 2017/745). This certification marks COMAR's compliance with the most stringent European Union medical device standards, demonstrating their commitment to excellence and their ability to provide high-impact solutions to the market.
The new EU MDR introduces more rigorous requirements for the safety and performance of medical devices, aiming to ensure patient safety and device traceability. COMAR's successful certification is a testament to their dedication to meeting these standards and delivering safe and reliable medical devices to their customers.
With this certification, COMAR can continue to sell CE-marked Oral/Topical Dispensing Devices in the European Union, specifically Class I devices with a measurement function and Class I non-measuring devices, which are press-in bottle adapters. The certification covers a wide range of COMAR's products, including Oral Syringes, Dosage Cups AccuCup®, Dosage Spoons, Dosage Scoops, and Dropper Assemblies.
Sonia Hardikar, VP of Quality and Regulatory Affairs at COMAR, expressed her pride in the company's achievement, stating, "Receiving the new CE certificate under the EU MDR is a testament to the dedication and hard work of our entire team. This accomplishment reflects our unwavering commitment to delivering safe and reliable medical devices to our customers. We are excited to continue serving our European clients while exploring new opportunities with this certification."
COMAR's success in obtaining the CE certification under the EU MDR is the result of the tireless efforts and dedication of their entire team. The company extends its heartfelt gratitude to everyone involved in this significant milestone, including their valued customers and the certification body and auditors who collaborated with them throughout the process.
This achievement not only solidifies COMAR's position as a trusted provider of medical devices and packaging solutions in the European market but also sets the stage for continued growth and innovation in the medical and pharmaceutical device sectors. With their commitment to excellence and their ability to meet the most stringent regulatory standards, COMAR is well-positioned to explore new opportunities and continue delivering high-impact solutions to their customers.
COMAR's success in obtaining the CE certification under the EU MDR is a clear demonstration of their unwavering commitment to progress and innovation. As they continue to push the boundaries of what is possible in the medical devices and packaging solutions industry, COMAR remains dedicated to delivering safe, reliable, and high-quality products to their customers around the world.
