QMS Compliance and Remediation – We’ve got you covered!
Failure to meet regulatory standards can lead to product recalls, fines, and reputation damage that can put a strain on your resources and disrupt business operations. If you need help implementing a new QMS, maintaining compliance, or require remediation due to audit findings, a recall, or an FDA Form 438 or Warning Letter, we can help.
QMS compliance services:
- QMS implementation
- Full or partial internal audits
- Pre-assessment audits
- Gap analysis
- Transition support
QMS remediation services:
- Nonconformance remediation
- FMEA or fault tree investigations
- CAPA procedures
- FDA Form 483 (Inspectional Observations) and FDA Warning Letter response
- Nonconformance management procedure implementation to address deficiencies
- Field questions from you or the FDA during corrective action activities
Let us take the headache out of QMS compliance and remediation. Leverage our decades of experience and our ISO 13485-certified QMS system. Contact us today for a free consultation.
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.
