Supply Chain Management
At Southmedic, world-class supply chain management begins with our customers. Our customer-focused supply chain professionals strive for cost saving solutions to optimize the value proposition for each customer.
Our team is focused on four primary areas: reducing cost, improving quality, shortening delivery times, and implementing lean manufacturing process improvement methodologies.
Our goal at Southmedic is to provide full service supply chain management with an experienced and responsive team to complement every aspect of manufacturing, custom injection molding and business needs.
The management and employees of Southmedic Inc. are dedicated to providing our customers with high quality innovative products that always meet their needs by the use of our quality assurance system and procedures.
We are committed to compliance with regulatory requirements and to maintaining the effectiveness of the Quality Management System. Southmedic is proud of its many certifications and awards to service the global medical marketplace.
This commitment is further communicated through quality assurance objectives established at all levels of the organization, to ensure that it serves as the foundation of all that we do. Southmedic’s medical manufacturing division is totally committed to continuous process improvement for enhanced quality and reduced waste and process variability. We have an excellent quality assurance reputation in the medical industry and an outstanding track record for developing innovative medical devices.
Certifications and Registrations
Southmedic specializes in the manufacturing of products for the medical, cosmetic and electronic industries. In addition, we have earned a worldwide reputation for quality, product design and innovation in the manufacturing of medical anesthetic components.
For more information about our certifications and registrations
MDSAP 675962 – ISO 13485:2016
FM 643600 – ISO 13485:2016
CE 644824 – Annex V
CE 644823 – Annex II
Medical Device Establishment Licence
Southmedic recognizes that regulatory compliance is an essential requirement in the medical device industry and achieved initial certification to ISO standards in 1996. When you choose Southmedic as your OEM supplier, you are selecting a supplier that is: MDSAP certified, ISO 13485 certified, European MDD certified, and FDA registered. We can provide the necessary support in determining the regulatory requirements of your product whether it be determining device classification, guiding 510k documentation, conducting risk analysis or assessing post-market considerations. Southmedic offers a comprehensive analysis of requirements. Core competencies include: Design – Tooling – Cleanroom Injection Molding – 100,000 Clean Room Assembly – Packaging – Distribution – Regulatory Affairs Support Services.