HCM's Commitment to Quality
HCM’s CGMP manufacturing facility and operations are designed to meet current drug and device regulations including ISO and European guidelines for aseptic filling of parenteral products. Current certifications include ISO 90001:2000 and ISO 13485. HCM has been inspected by the FDA.

Our quality systems are designed to meet your exacting requirements whether your products are drugs or devices. We have established
our Quality systems, documented in Standard Operating Procedures
(SOPs), to support the company’s quality goals.

 

 

Mission Statement
To be a leading provider of process scale-up development and aseptic filling services ranging from feasibility to cGMP, including stability testing. As a company we are committed to quality, innovation, continuous improvement and regulatory compliance. We take pride in meeting the unique needs of each client. Employees are provided a supportive work environment with opportunities for growth.

 

 FDA INSPECTED FOR DRUG AND MEDICAL DEVICE
Directions to HCM....Career Opportunities at HCM

99 South Bedford Street, Burlington, MA 01803 Phone: 781-270-7900 X114 Fax: 781-270-7899 e-mail: info@hyaluron.com 2007 Hyaluron, Inc