| Starts: | Tuesday December 02, 2008 at 4:00pm |
|---|---|
| Ends: | Tuesday December 02, 2008 at 7:00pm |
| Event Type: | Training/Seminar |
| Region: | San Francisco Bay Area |
| Location: |
Mission Bay Center at University of California San Francisco - UCSF 1675 Owens St San Francisco, CA 94158 US |
| Price: | |
| Website: | http://kalypso.eventbrite.com |
| Industry: | medical device |
| Keywords: | Medical Device, Life Sciences, Plm, Kalypso, Regulatory Affairs, Technology, Surgical Products, Devices, Medical Device Seminar, Product Development, Compliance |
| Intended For: | CIO, VP, Director, Manager; Quality, R&D, Regulatory Affairs, Document Control, Products, Technology, Product Development, Engineering, IT, Strategic Programs |
| Organization: | Life sciences, medical device |
Register for this free one hour session at http://kalypso.eventbrite.com.
For today's medical device companies, implementing new product development (NPD) processes that comply with increasing regulatory requirements is a challenge. Many companies have inadvertently deployed overly bureaucratic systems and, as a result, have found themselves with increasing - costs and slowing development.
Kalypso recently completed research to explore how leading medical device companies are balancing NPD with compliance requirements.
In this one hour session, speakers Noel Sobelman and Marcus Yoder of Kalypso will discuss best practice models for maintaining compliance while streamlining NPD. Additionally, they will explore leading industry practices revealed in Kalypso's study including:
- Project Governance and Decision Making
- Process Structure
- Project Team Organization
- Portfolio Management
- Software Systems & Tools
All seminar participants will receive a copy of Kalypso's exclusive white paper Beyond Compliance: Medical Device Product Development. The session will conclude with Q&A and be immediately followed by a cocktail reception.
Register today at http://kalypso.eventbrite.com