CSSC Holds Regulatory Seminar; Industry Experts to Focus on Quality Initiatives
MORRISTOWN, N.J.–(BUSINESS WIRE)–Sept. 21, 2006–CSSC, a leading provider of regulatory compliance and validation solutions to the life sciences industry, today announced that it will be holding a complimentary seminar, “Leveraging Your Investment in Quality,” on October 4 from 5:30 p.m. – 7:30 p.m. at the Residence Inn Boston Cambridge, 6 Cambridge Center Drive, Cambridge, MA. Hearty hors d’oeuvres and refreshments will be served.
The seminar will feature speakers from CSSC as well as CSSC partners and clients, and will address several critical areas of compliance, including:
— Focusing Your Compliance Efforts Using Risk Assessment
— The Site Validation Master Plan as a Road Map for Clinical Manufacturing Compliance
— The Validated, Paperless Laboratory
Presenting from CSSC are George Kuniholm and Rob Finamore. George is Regional Director for CSSC, Inc.’s New England Office in Cambridge, Massachusetts. George also serves as Vice President of NERCSQA. Rob, a Senior Validation Manager at CSSC, is a recognized expert in computer system validation and 21 CFR Part 11 compliance. Also presenting are Carolyn Stockdale, Associate Director of Millennium Pharmaceuticals, Inc., and Victoria Lander, Corporate Compliance Manager, Waters Corporation.
Commented Raymond Roggero, President and Chief Operating Officer of CSSC, “The Cambridge area is a hub for the pharmaceutical and biotechnology industries. Whether start-up, mid-size, or mature, all life science companies face compliance challenges. Learning to address them at the right time, with the right resources, and with the appropriate level of effort will help them focus on their critical mission of bringing products to market as quickly as possible.”
To register for the seminar, please contact Nancy Malagold at nancy.malagold@csscinc.net.
About CSSC, Inc.
CSSC, Inc., headquartered in Morristown, New Jersey, provides full-service regulatory compliance services and consulting. CSSC has more than 80 employees in six locations throughout the United States and a strategic partnership in Europe to service clients worldwide. Founded in 1994, CSSC offers a complete range of compliance solutions to the pharmaceutical, biotechnology, and medical device industries, including comprehensive validation services, project management, Quality System Regulation consulting, 21 CFR Part 11 services, PDMA compliance solutions, auditing, and training. CSSC scientists, engineers, pharmacists, and project management professionals are respected throughout the industry for their knowledge and experience. For more information, visit www.csscinc.net.
