9/22-23, San Jose, CA; By ProSystem and Oracle; Focus:
- Impact of IEC 80001-1 for Medical Device and IT- industries Future Regulations & Regulatory Requirements - Clinical Evaluation for all Medical Devices in Europe - Expectations of European Notified Bodies on Technical Files when auditing after March 2010 - Intensive training sessions on recognized and harmonized standards on Usability (IEC 62366) – Software (IEC 62304) – Risk-Management (ISO 14971)
Regular (Listed) fees : $795 per day, $1495 for both days ((Discount may be available to qualified applicants)).
More details at http://www.prosystem-usa.com/ For further information please contact: Mrs. Sima Niknafs Phone 619-595-4875 Fax 619-595-3150 sima.niknafs@prosystem-usa.comThis e-mail address is being protected from spam bots, you need JavaScript enabled to view it
