| |
|
|
| |
|
|
| |
HUM-MOLGEN
-> Events
-> Courses and Workshops |
|
|
| |
| |
| |
March 02, 2006 |
|
|
| |
|
|
| |
|
|
|
SPI USA, Inc., Minneapolis, MN
August 10-11, 2006
This 2-day workshop presented by SPI USA, Inc. in collaboration with CardioMed Device Consultants, LLC. will aid you in learning and understanding such topics as: How to interact with the FDA; Device Classification, and Regulatory Requirements to Pre-market Approval (PMA); the FDA Inspection Process; Quality Systems Regulations and more!
|
|
|
|
|
|
|
|
Organized by:
|
|
SPI USA, Inc. |
|
|
Invited Speakers:
|
|
Former FDA Scientific Reviewer, Dr. Semih Oktay and Dr. Antonio Moreira, Executive Vice President of SPI USA, Inc.
|
|
|
|
|
|
|
|
Deadline for Abstracts:
|
|
n/a
|
|
|
|
|
|
|
|
Registration:
|
|
Please see website for details!
|
|
|
E-mail:
|
|
nhawkins@usaspi.com
|
|
|
|
|
|
|
|
|
|
|
|
|
|
| |
|
|
|
|
|
|
|
|
|
|
|
|
|
Generated by meetings and positions 5.0 by Kai Garlipp
WWW: Kai Garlipp,
Frank S.
Zollmann.
7.0 © 1995- HUM-MOLGEN. All rights reserved.
Liability, Copyright and Imprint. |
|