AGAWAM, MASS. – December 3, 2007 – A new, free white paper, addressing the challenges of new U.S. Food and Drug Administration (FDA) regulations awaiting combination products manufacturers, is now available for download at www.microtestlabs.com/combinationpaper.
While combination products are experiencing dramatic growth, the convergence of drug/biologics and devices brings a host of regulatory challenges. Manufacturers must ensure their products meet cGMP practices as well as pass muster with the FDA, ISO, and USP.
Steven Richter, Ph.D., Microtest President & Chief Scientific Officer, addresses the critical issues associated with this complex process, including defining the FDA’s regulatory framework, reviewing developments in FDA thinking, and identifying future considerations in developing effective quality assurance systems.
“The combination products market – medical devices embedded with pharmaceutical or biologics components –is rapidly moving forward with a new direction and emphasis regarding product safety and FDA requirements,” said Richter, who is author of the announced white paper, “Combination Products: Navigating Two FDA Quality Systems.”
Navigant consulting, estimating the combination products market at $5.9 billion in 2004, predicts a nearly $9.5 billion market in 2009. In 2005, the FDA received 275 combo product submissions, and an estimated 30% of new products under development today are combo products.
“For manufacturers, the convergence of devices and drugs or biologics also brings a host of new FDA testing guidelines, practices, and regulations unique to the development and production of combination products,” he said.
The paper’s contents include: Defining the Convergence, FDA Responsibility, QC Drug Release Criteria, Biologics, New Developments in FDA Thinking, and Future Considerations.
Download the free white paper at: www.microtestlabs.com/combinationpaper. For more information visit Microtest on the Web at www.microtestlabs.com, or call toll-free: 1-800-631-1680.
About Microtest
Microtest is a leader in testing services and contract manufacturing for the medical device, pharmaceutical, biotechnology industries. Based in Agawam, Massachusetts, USA, the company’s expertise and flexible processes enhance product safety and security, accelerate time to market, and minimize supply chain disruption. For more information, visit www.microtestlabs.com or call 1-413-786-1680 or toll-free 1-800-631-1680.
# # #
Public Relations contact: Tiziani Whitmyre Inc., http://www.tizinc.com
Technorati tags: Microtest, FDA regulations, white paper, whitepaper, combo products, combination products
Tags: combination products, combo products, FDA regulations, Microtest, white paper, whitepaper
Technorati tags: 
