At Biomedical Polymers state-of-the-art inspection and monitoring equipment are implemented to ensure defect prevention. Our quality assurance system and document control conforms to 21 CFR part 820 cGMP requirements. Document masters are filed both electronically and in a hard copy master file. A formal engineering change order is required at any system modification stage. The system allows for complete lot traceability and can be enhanced to meet customers needs to comply with specific regulatory requirements.

• Toll Free : 800-253-3684
• Phone : 978-632-2555
• sales@biomedicalpolymers.com