1MED Unveils Solutions for Medical Device Companies at Outsourcing in Clinical Trials: Medical Devices Europe Conference
Munich, Germany – March 8, 2024
1MED, a leading Contract Research Organization (CRO) specializing in clinical and regulatory support for medical device companies, is thrilled to participate as a sponsor and exhibitor at the 12th Annual Outsourcing in Clinical Trials: Medical Devices Europe Conference in Munich. This year’s conference, held from March 8-9, 2024, brings together industry leaders, experts, and stakeholders to discuss the latest advancements, challenges, and opportunities in the medical device sector.
Supporting Medtech Companies in Meeting MDR Deadlines
With the Medical Device Regulation (MDR) fully applicable to all medical devices from May 27, 2024, 1MED is committed to providing comprehensive solutions that assist medtech companies in meeting the crucial 2024 MDR deadlines. The company’s offerings include the 1MED Compliance Pack and the 1SURVEY Real-World Data collection tool.
1MED Compliance Pack
The 1MED Compliance Pack is an invaluable tool designed to facilitate the recertification process for medical device companies. This tool addresses the challenges associated with MDR compliance by identifying documentation gaps and streamlining the submission process to Notified Bodies. By utilizing the 1MED Compliance Pack, companies can simplify compliance with the MDR’s stringent standards and ensure the timely recertification of their medical devices.
1SURVEY Real-World Data Collection Tool
1MED also introduces 1SURVEY, an innovative digital platform that enables medical device manufacturers to collect and analyze real-world data. 1SURVEY empowers companies to make informed, data-driven decisions and improve patient care through proactive measures. The platform streamlines the process of generating questionnaires, digital implementation, and data collection, providing a comprehensive solution for gathering clinically relevant information on medical devices.
1MED’s Commitment to Innovation and Expertise
Enrico Perfler, founder of 1MED, emphasized the significance of the Outsourcing in Clinical Trials conference as a platform for the European medtech and diagnostics community to gain valuable insights into regulatory changes and strategies for addressing them. He highlighted 1MED’s dedication to innovation and its commitment to providing exceptional assistance to companies navigating the complexities of the new regulatory framework.
Navigating Critical Deadlines for Medical Device Recertification
The year 2024 presents critical deadlines for the medtech sector, particularly in terms of recertifying legacy devices under the new MDR. By May 26, 2024, companies must submit their legacy devices for recertification, and by September 26, 2024, they must secure agreements with Notified Bodies. 1MED’s solutions, including the 1MED Compliance Pack and 1SURVEY, are designed to help companies overcome these challenges and ensure compliance with the MDR’s requirements.
1MED’s Presence at the Outsourcing in Clinical Trials: Medical Devices Europe Conference
1MED’s participation as a sponsor and exhibitor at the Outsourcing in Clinical Trials: Medical Devices Europe Conference reflects the company’s commitment to supporting medtech companies in navigating the evolving regulatory landscape. 1MED’s experts will be available at Booth 12 to discuss the company’s solutions and provide personalized guidance to attendees.
About 1MED
1MED is a premier Contract Research Organization (CRO) dedicated to providing clinical and regulatory support to medical device companies. With extensive experience and deep expertise in the medtech sector, 1MED offers a comprehensive range of services to help companies navigate the complex regulatory environment and bring innovative medical devices to market. 1MED’s commitment to quality, innovation, and customer satisfaction has earned it a reputation as a trusted partner for medtech companies worldwide.
Call to Action
Visit 1MED at Booth 12 at the Outsourcing in Clinical Trials: Medical Devices Europe Conference to learn more about the company’s solutions and how they can help your company meet the challenges of the MDR. With 1MED as your partner, you can confidently navigate the regulatory landscape and bring your innovative medical devices to market.