Rochester, N.H. October 06, 2007 Phase II Medical Manufacturing today announced it is significantly expanding and upgrading its manufacturing facility with the addition of 1,500 square feet of clean room space and a new Enterprise Resource Planning (ERP) system, which uses a single-source platform to unify all the companys operations from human resources to finished product. This system allows Phase II Medical to maintain the quality and effectiveness its customers have come to expect. In addition, as part of its commitment to producing the highest quality medical devices possible, the company has hired three new engineers, a sales manager, a material manager and 20 additional assembly line workers. Phase II now employs 55 full-time employees and has a total of 3,000 square feet of clean room manufacturing and inspection space.
Phase II contracts with companies to produce medical devices in its state-of-the-art temperature-, humidity- and particulate-controlled clean rooms certified to Class 100,000. In addition to expert manufacturing, Phase IIs engineering staff can assist with the design of new products or enhancements to existing products. Once a design is finalized, the company engineers and implements the most cost-effective and efficient manufacturing process possible, and also offers pad printing, packaging and shipping services.
Our expansion, upgrade and hiring show that Phase II is committed to providing its customers with the best possible quality when it comes to medical device manufacturing, said Adam Prime, President of Phase II. It is very clear that our pricing and services make Phase II an attractive option for companies that insist on an FDA-approved, ISO 9001 and ISO 1345 compliant and certified manufacturer.
Phase II offers companies design services, as well as manufacturing. For New Wave Surgical in New York, Phase II received the conception of a Defogging Heated Endoscopic Lens Protector. Phase II moved this product from conception up to its current levels of 1,000 units a month. Phase II is the also the manufacturer of choice for several large companies, including a global manufacturer which specializes in surgical navigation and TissueLink Medical in Dover, N.H., which specializes in cautery devices. The Phase II Medicals transition and expansion will permit it to run more efficiently and better serve its current customers, as well as position itself to add new customers and potentially boost employment opportunities within the state of New Hampshire.
About Phase II Founded in 1995 to serve the single-use medical product and device industry, Phase II Medical Manufacturing now provides design, development, manufacturing, packaging, shipping, and sterilization services to its customers. FDA registration, Canadian licensing, and ISO 9001:2000 and ISO 13485:2003 certification are maintained to ensure that current U.S. and international standards are satisfied. Phase II works closely with clients on a regular basis to ensure all devices meet or exceed specifications, and its commitment and dedication to customers is unmatched in the industry.For more information please visit www.phaseiimed.com
