We are thrilled to share that i+Med has successfully obtained the MDR certification for their groundbreaking product, Daydrop! 🎉
The Medical Device Regulation (MDR) certification is a significant milestone, reflecting i+Med’s unwavering commitment to safety, efficacy, and innovation in healthcare. Daydrop, eye drops for dry eye, known for its cutting-edge technology of controlled release technology of ectoin and superior quality, now meets the highest European standards for medical devices.
This achievement is not just a testament to the hard work and dedication of the i+Med team but also a giant leap forward in advancing medical technology. With MDR certification, Daydrop is set to transform patient care, offering reliable and effective solutions that adhere to the strictest regulatory requirements.
Congratulations to the entire i+Med team for this remarkable accomplishment! Let’s continue to push the boundaries of innovation and make a positive impact on healthcare globally.