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CONTACT US |
The PolyOne Difference
| Delivering value by helping customers manage risk |
Food & Drug Administration (FDA) |
- More than 30 cGMP (FDM & ISO 13485) facilities worldwide dedicated to medical manufacturing to deliver the highest quality product
- Our Product Stewardship program aims to deliver compliance with global regulatory standards
- Our global footprint reduces qualification costs and risk of supply chain outages
- Regulatory-compliant materials and drug master files facilitate commercialization
- PolyOne’s “No Surprises Pledge” demonstrates our commitment to safe and environmentally-sound solutions
- Dedicated healthcare resources provide rapid responses to the most challenging material questions
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The United States Food & Drug Administration (FDA), a government agency, is responsible for regulating and supervising the safety of foods, tobacco products, dietary supplements, medications, drugs, vaccines, biopharmaceuticals, blood transfusions, medical devices, electromagnetic radiation emitting devices, veterinary products, and cosmetics. Read more...
Good Manufacturing Practices (GMP)
The Food and Drug Administration (FDA) Good Manufacturing Practices (GMP) are enforced in the US by the FDA. As a responsible partner PolyOne has established an internal GMP program for the manufacture of PolyOne products intended for use in food, drug and medical (FDM) applications. Read more...
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