International Events

                                  July 2008

Organizer Date Location Event
The Center for Professional Innovation and Education(CFPIE) Jul
07 - 08 		costa mesa ,CA, United State Aseptic Processing in the Manufacture of Biotech and Pharmaceutical Products
The Center for Professional Innovation and Education(CFPIE) Jul
07 - 09		 malvern, PA, United State Current Good Laboratory Practices & Current Good Manufacturing Practices - A Basic Primer
Medilink Jul
07 - 09		 Amsterdam, Netherlands Preparation, Packaging & Labelling of Clinical Trial Material
The Center for Professional Innovation and Education(CFPIE) Jul
10 - 11		 Orange County/Costa Mesa, CA, United State Overview Of FDA Regulatory Compliance For Medical Devices
Management Fourm Jul
10 - 11		 London, United Kingdom US FDA APPROVAL PROCESS FOR MEDICAL DEVICES
British Standardization Institute Management Systems Jul 21st Malaysia ISO 9001:2000 (Quality Management) Understanding of Requirements
The Center for Professional Innovation and Education(CFPIE) Jul
21 - 22		 Malvern, PA, United State Validation of Computer Systems
The Center for Professional Innovation and Education(CFPIE) Jul
21 - 23		 Orange County/Costa Mesa, CA, United State Technical Writing for the Pharmaceutical, Medical Device, and Biotech Industries
Management Fourm Jul 2nd London, United Kingdom LABELLING AND INSTRUCTIONS FOR USE FOR MEDICAL DEVICES AND IVDS
British Standardization Institute Management Systems Jul
23 - 24		 Malaysia ISO 9001:2000 (Quality Management) Internal Audit
Center of Professional Advancement Jul
28 - 30		 New Brunswick, NJ, United State Process Validation for Packaging of Pharmaceuticals and Medical Devices

                               August 2008

Organizer Date Location Event
British Standardization Institute Management Systems Aug
04 - 06		 Malaysia ISO 13485:2003 (Medical Devices) Implementing ISO 13485:2003
British Standardization Institute Management Systems Aug
05 - 06		 Malaysia ISO 9001:2000 (Quality Management) Quality System Documentation
Center of Professional Advancement Aug 11th New Brunswick, NJ, United State cGMP Auditing - Strategies for Compliance
Center of Professional Advancement Aug
12 - 13		 New Brunswick, NJ, United State Preparing for and Surviving an FDA Inspection
Medilink Aug
14 - 17		 Hong Kong, China Hong Kong International Medical & Healthcare Fair 2008
The Center for Professional Innovation and Education(CFPIE) Aug
20 - 22		 costa mesa ,ca, United State Process Validation for Medical Devices
British Standardization Institute Management Systems Aug
25 - 29 		Malaysia ISO 9001:2000 (Quality Management) Lead Auditor


                          September 2008

Organizer Date Location Event
British Standardization Institute Management Systems Sep 3rd Malaysia ISO 13485:2003 (Medical Devices) Understanding Medical Device Requirements
British Standardization Institute Management Systems Sep
03 - 04 		Malaysia ISO 9001:2000 (Quality Management) Implementing an ISO 9001:2000 QMS
Center of Professional Advancement Sep
04 - 05		 New Brunswick, NJ, United State Calibration in the FDA Regulated Industry
Center of Professional Advancement Sep
08 - 10
Burlingame, CA, United State
 Analytical Methods Validation for FDA Compliance
The Center for Professional Innovation and Education(CFPIE) Sep
10 - 11		 Dublin, Ireland Good Monitoring Practices for Medical Devices
Medilink Sep
11 – 13		 Buenos Aires, Argentina ExpoMedical 2008
British Standardization Institute Management Systems Sep 15th Malaysia ISO 9001:2000 (Quality Management) Understanding of Requirements
Management Fourm Sep
18 - 19		 London, United Kingdom MEDICAL DEVICE CLINICAL INVESTIGATIONS AND EVALUATIONS
British Standardization Institute Management Systems Sep
23 - 24		 Malaysia ISO 9001:2000 (Quality Management) Internal Audit
Center of Professional Advancement Sep
22 - 24		 New Brunswick, NJ, United State ISO 13485, ISO 9001 and QSR Regulations for Medical Device Companies
Association for the Advancement of Medical Instrumentation(AAMI) Sep
22 - 26		 San Diego, United State Quality System Requirements and Industry Practice
The Center for Professional Innovation and Education(CFPIE) Sep
22 - 23		 Orange County/Costa Mesa, CA, United State Validation of Computer Systems
The Center for Professional Innovation and Education(CFPIE) Sep
22 - 23		 Dublin, Ireland Design Control for Medical Device Professionals
Management Fourm Sep
22 - 23		 London, United Kingdom DRUG DEVICE COMBINATIONS PRODUCTS
Informa Life Sciences Sep
22 - 25
Brussels, Belgium
 Labelling and Packaging Compliance for Medical Devices and In Vitro Diagnostics
East Wood Park Sep 22 -
Oct 3rd		 United Kingdom Biomedical equipment maintenance practice
Informa Life Sciences Sep
23 - 25		 Brussels, Belgium Medical Device Law and Compliance
Medilink Sep
24 - 25		 Ireland Medtec Ireland 2007 (Exhibition)
Singapore Exhibition Services Sep 29th London, United Kingdom MEDICAL DEVICE REGULATORY AFFAIRS IN THE MIDDLE EAST



                             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
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
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
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



                            November 2008

Organizer Date Location Event
Center of Professional Advancement Nov
03 - 05		 New Brunswick, NJ, United State Medical Device Regulatory Compliance
Center of Professional Advancement Nov
03 - 05		 New Brunswick, NJ, United State Complaint Handling and MDR Reporting
Center of Professional Advancement Nov
03 - 05		 New Brunswick, NJ, United State Validation of Manufacturing and Distribution Computer Systems
Association for the Advancement of Medical Instrumentation(AAMI) Nov
03 - 05
Las Vegas, NV, United State
 Software Validation Requirements and Industry Practice
Association for the Advancement of Medical Instrumentation(AAMI) Nov
03 - 05		 San Diego, United State Building a quality management system in a regulated environment : A 13485 Workshop
The Center for Professional Innovation and Education(CFPIE) Nov
10 - 11		 malvern, PA, United State Aseptic Processing in the Manufacture of Biotech and Pharmaceutical Products
British Standardization Institute Management Systems Nov
10 - 12		 Malaysia ISO 13485:2003 (Medical Devices) Implementing ISO 13485:2003
Association for the Advancement of Medical Instrumentation(AAMI) Nov
10 - 13		 Arlington, United State Radiation Sterilization for Medical Devices
British Standardization Institute Management Systems Nov  15th Malaysia ISO 9001:2000 (Quality Management) Understanding of Requirements
Center of Professional Advancement Nov
11 - 12		 Amsterdam, Netherlands Root Cause Investigation for CAPA
The Center for Professional Innovation and Education(CFPIE) Nov
13 - 14		 Malvern, PA, United State Medical Devices: EU Directives, Guidance, CE Marking and ISO Standard Certifications
The Center for Professional Innovation and Education(CFPIE) Nov
17 - 18		 malvern, PA, United State Comprehensive Overview of FDA Regulatory Compliance for Drugs and Biotech Products
British Standardization Institute Management Systems Nov
18 - 19		 Malaysia ISO 9001:2000 (Quality Management) Internal Audit
Management Fourm Nov
20 - 21		 London, United Kingdom INTRODUCTION TO THE MEDICAL DEVICES DIRECTIVES



                           December 2008

Organizer Date Location Event
British Standardization Institute Management Systems Dec 1st Malaysia ISO 13485:2003 (Medical Devices) Understanding Medical Device Requirements
British Standardization Institute Management Systems Dec
03 - 04 		Malaysia ISO 9001:2000 (Quality Management) Implementing an ISO 9001:2000 QMS
The Center for Professional Innovation and Education(CFPIE) Dec
01 - 02		 Malvern, PA, United State Overview Of FDA Regulatory Compliance For Medical Devices
Association for the Advancement of Medical Instrumentation(AAMI) Dec
01 - 03
San Diego, United State
 Design Control Requirements and Industry Practice
Center of Professional Advancement Dec
01 - 03		 Amsterdam, Netherlands Auditing and Inspecting Preclinical Research for GLP Compliance
The Center for Professional Innovation and Education(CFPIE) Dec
03 - 04		 Orange County/Costa Mesa, CA, United State Good Monitoring Practices for Medical Devices
The Center for Professional Innovation and Education(CFPIE) Dec
03 - 05		 Malvern, PA, United State Reporting Failure Investigations and Process Deviations
Center of Professional Advancement Dec
04 - 05		 Amsterdam, Netherlands The GLP Study Director
The Center for Professional Innovation and Education(CFPIE) Dec
08 - 10		 Malvern, PA, United State Technical Writing for the Pharmaceutical, Medical Device, and Biotech Industries
Association for the Advancement of Medical Instrumentation(AAMI) Dec
08 - 11		 Arlington, VA, United State Quality System Requirements and Industry Practice
Center of Professional Advancement Dec
08 - 11		 Amsterdam, Netherlands Fundamentals of Biotechnology
Center of Professional Advancement Dec
08 - 10		 Amsterdam, Netherlands Commissioning, Qualification and Validation
Association for the Advancement of Medical Instrumentation(AAMI) Dec
8 - 12		 Arlington, VA, United State Quality System Requirements and Industry Practice
Center of Professional Advancement Dec
15 - 17		 Amsterdam, Netherlands System Validation, GAMP Harmonization and P.A.T
British Standardization Institute Management Systems Dec
15 - 19
Malaysia
 ISO 9001:2000 (Quality Management) Lead Auditor