You want to get your product to market as quickly as possible, but to do so, you need to ensure you are complying with the strict regulations mandated across the medical device industry. Failing to do so can put your business—and more importantly, your end-users—at risk. Navigating the murky waters of the European Union’s (EU) conformité européenne (CE) Mark regulatory requirements, and knowing which ones your device is subject to, can be daunting, even for the most established medical device manufacturers. This is especially true with the EU’s transition from the Medical Device Regulation (MDR) system to the In Vitro Diagnostic Regulation (IVDR) system.
Sterling can help.
Before bringing a medical device to market in the EU and other parts of the world that follow CE Mark regulation, it is essential to determine applicable regulatory requirements it must adhere to in order to ensure patient and user safety. With Sterling’s regulatory strategy support, we offer services to help you identify and address key CE Mark requirements for your device including:
- Overall EU regulatory strategy support
- EU MDR gap analysis and assessment for CE Mark
- CE Mark documentation support, specifically:
- EU MDR to IVDR submission documentation gap analysis
- Transitioning from U.S. Food and Drug Administration (FDA) submission to CE Mark submission
- Transitioning from Medical Devices Directive (MDD) submission to MDR submission
- Other submissions to MDR submission
- EU MDR/IVDR documentation compilation and submission
- EU MDR/IVDR documentation remediation
- Notified body communication support services
- MDR clinical evaluation report support services, specifically:
- EU MDR CER gap analysis
- Transitioning from FDA submission to CE Mark submission
- Transitioning from MDD submission to IVDR submission
- Other submissions to IVDR submission
- EU MDR CER development and transition support
- EU MDR CER remediation
- EU MDR CER gap analysis
- IVDR Performance Evaluation Report (PER) support services, specifically:
- EU IVDR PER gap analysis
- EU IVDR PER development and transition support
- EU IVDR PER remediation
At Sterling, we understand the legal requirements for marketing your product in the EU. When it comes to the increasingly complex world of regulatory submissions, we’ve got you covered.
About Sterling Medical Devices
Sterling Medical Devices specializes in the design, development, and test of medical devices. Sterling addresses every aspect of the development process: software, electronics, mechanical, quality, and compliance. Our goal is to make sure you get the FDA approval and CE Marking you need to bring your device to market. Sterling Medical Devices has developed more than 1,000 medical device products for over 300 companies, ranging from Class II diagnostic and therapeutic systems to Class III implantable devices, using embedded systems, PC based devices, smartphones/tablets, and web/cloud services. We are proud to have worked with such prestigious organizations as Covidien, St. Jude Medical, Medtronic, Boston Scientific, Johnson & Johnson, and many more. We also partner with early-stage companies to help them bring new products to market. In every case, we produce the right product in the right time frame with the right budget.
