|
October 2008 |
| Organizer |
Date |
Location |
Event |
| The Center for Professional Innovation and Education(CFPIE) |
Oct
01 - 03 |
malvern, PA, United State |
Process Validation for Medical Devices |
| Center of Professional Advancement |
Oct
01 - 03 |
New Brunswick, NJ, United State |
Critical Process Cleaning and Cleaning Validation |
| The Center for Professional Innovation and Education(CFPIE) |
Oct
01 - 03 |
Dublin, Ireland |
Technical Writing for the Pharmaceutical, Medical Device, and Biotech Industries |
| Association for the Advancement of Medical Instrumentation(AAMI) |
Oct
01 - 03 |
| Arlington, VA, United State | |
Integrating Risk Management into the Quality System |
| Management Fourm |
Oct
02-03 |
London, United Kingdom |
US FDA Medical Deivce QS Regulations (cGMPS) and Requirements |
| Center of Professional Advancement |
Oct
06 - 07 |
New Brunswick, NJ, United State |
Design Control and Product Validation |
| East Wood Park |
Oct
06 - 08 |
United Kingdom |
Servicing ventilation equipment |
| Center of Professional Advancement |
Oct
07 - 09 |
Burlingame, CA, United State |
Commissioning, Qualification and Validation |
| Center of Professional Advancement |
Oct
09 - 10 |
Amsterdam, Netherlands |
Clean Room Technology |
| East Wood Park |
Oct
13 - 15 |
United Kingdom |
Servicing anaesthetic equipment |
| Center of Professional Advancement |
Oct
13 - 15 |
Amsterdam, Netherlands |
Radiation Curing: Ultraviolet Light and Electron Beam Technology |
| Association for the Advancement of Medical Instrumentation(AAMI) |
Oct
13 - 16 |
Arlington, VA, United State |
Industrial Sterilization for Medical Devices |
| British Standardization Institute Management Systems |
Oct
15 - 16 |
Malaysia |
ISO 9001:2000 (Quality Management) Quality System Documentation |
| The Center for Professional Innovation and Education(CFPIE) |
Oct
15 - 17 |
costa mesa , ca, United State |
Current Good Laboratory Practices & Current Good Manufacturing Practices - A Basic Primer |
| Center of Professional Advancement |
Oct
15 - 17 |
New Brunswick, NJ, United State |
Lyophilization Technology |
| The Center for Professional Innovation and Education(CFPIE) |
Oct
16 - 17 |
malvern, PA, United State |
Effective Quality Assurance Auditing for FDA Regulated Industries |
| Management Fourm |
Oct
16-17 |
London, United Kingdom |
Medical Device Regulation in Asia |
| Center of Professional Advancement |
Oct
20 - 22 |
New Brunswick, NJ, United State |
Good Laboratory Practices (GLP) |
| Center of Professional Advancement |
Oct
20 - 22 |
Burlingame, CA, United State |
In Vitro Testing Methodologies |
| The Center for Professional Innovation and Education(CFPIE) |
Oct
20 - 21 |
Dublin, Ireland |
Medical Devices: EU Directives, Guidance, CE Marking and ISO Standard Certifications |
| Association for the Advancement of Medical Instrumentation(AAMI) |
Oct
20 - 24 |
London, United Kingdom |
Quality System Requirements and Industry Practice |
| British Standardization Institute Management Systems |
Oct
20-24 |
Malaysia |
ISO 9001:2000 (Quality Management) Lead Auditor |
| Synergus Medtech Consulting |
Oct
23-24 |
Copenhagen
Denmark |
Medical Device Regulation and Registration in China |
| The Center for Professional Innovation and Education(CFPIE) |
Oct
27-29 |
Barlin , Germany |
Process Validation for Medical Devices |
| Association for the Advancement of Medical Instrumentation(AAMI) |
Oct
27-29 |
Arizona, United State |
Process Validation Requirements and Industry Practice |
Center of Professional
Advancement |
Oct
27-29 |
Dublin, Ireland |
Analytical Methods Validation for FDA Compliance |
| Management Fourm |
Oct
30-31 |
London, United Kingdom |
Essential Guide to Clinical Trial Regulations |