Medical Device and Pharmaceutical Manufacturing Series Announced
FOR IMMEDIATE RELEASE
Contact Information:
Scott Whitlock
President
317.813.5411
scott.whitlock@flexwareinnovation.com
9128 Technology Lane
Fishers, IN 46038
Medical Device and Pharmaceutical Manufacturing Series Announced
Fishers, IN – March 10, 2005 – The Indiana Health Industry Forum, in conjunction with Purdue University’s Krannert Executive Education Programs, Flexware Innovation, and Camstar Systems, announces a series of seminars aimed at pharmaceutical and medical device manufacturers. The series consists of three sessions geared for Manufacturing, Quality, and Regulatory Executives and their teams, and will address preserving good business practices by fusing technology with compliance requirements.
Joseph Vinhais of Campbell, CA will facilitate the three sessions. Vinhais, a nationally-recognized presenter and author, is one of the country’s leading authorities on the subject of Regulatory Compliance.
“Joseph has spent the last ten years educating executives of FDA Regulated manufacturers,” noted Scott Whitlock, President and CEO of Flexware. “Participants will benefit from his insight in balancing manufacturing processes and FDA compliance in an effort to cut costs and improve efficiency.”
All sessions are being held at Purdue University’s Office of Engagement at Intech Park on Indianapolis’ west side. Each session will be held from 2:00 p.m. – 5:00 p.m. The first session on March 23, 2005 is entitled, “Risk Management in Life Science Manufacturing.” On April 19, Vinhais will discuss “The Perfect Device/Batch History Record – Electronic: Static vs Dynamic.” The final session, “The Cost of Compliance – Linking Compliance to Business Performance Drivers of Life Science Manufacturing,” will be held May 19.
