International Events

                            February 2009

Organizer Date Location Event
The Center for Professional Innovation and Education(CFPIE) Feb
02 to 03
 Orange County, CA, US Design Control for Medical Device Professionals
The Center for Professional Innovation and Education(CFPIE) Feb
02 to 03 		Malvern, PA USA Software Development for Medical Device Professionals
The Center for Professional Innovation and Education(CFPIE) Feb
09 to 10 		Malvern, PA USA FDA Inspections of Clinical Data Systems
The Center for Professional Innovation and Education(CFPIE) Feb
09 to 10		 Orange County, CA, US Practical Methods for Project Management
Management Forum Feb
12 to 13		 London, Uk REVISION TO THE MEDICAL DEVICE DIRECTIVES

British Standardization Institute Management Systems		 16th Feb     Northampton, UK Introduction to BS OHSAS 18001:2007
Management Forum
Feb
23 to 24
London, Uk MEDICAL DEVICE REGULATORY AFFAIRS IN LATIN AMERICA
Medilink Feb
23 to 27         		Japan Healthcare Trade Mission To Japan
British Standardization Institute Management Systems Feb
23 to 27		 County Durham, UK OH&S Management Systems Auditor/Lead Auditor (IRCA Certified)
Medilink Feb
27 to 28		 India Indian Medical Device & Plastic Disposables Industry 2009

                                March 2009

Organizer Date Location Event
British Standardization Institute Management Systems 2nd March Stratford,Uk Introduction to BS OHSAS 18001:2007
The Center for Professional Innovation and Education(CFPIE) March
03 to 04		 Malvern, PA USA FDA Inspections: What To Expect And How To Prepare
British Standardization Institute Management Systems March
03 to 04		 Stratford,Uk Implementing a BS OHSAS 18001 Management System
Center of Professional Advancement March
04 to 05 		London, UK EU REIMBURSEMENT FOR MEDICAL DEVICES
Medilink 5th March Chiswick, UK Introduction to Medical Device Directive 93/42/EEC (MDD)
The Center for Professional Innovation and Education(CFPIE) March
05 to 06		 Stratford upon Avon, UK BS OHSAS 18001 Internal Auditor
British Standardization Institute Management Systems 9th March
 Manchester, UK Introduction to BS OHSAS 18001:2007
British Standardization Institute Management Systems         March 09 to 13   Heathrow, UK OH&S Management Systems Auditor/Lead Auditor (IRCA Certified)
British Standardization Institute Management Systems         March 10 to 11 Manchester, UK Implementing a BS OHSAS 18001 Management System
British Standardization Institute Management Systems         March 12 to 13 Manchester, UK    BS OHSAS 18001 Internal Auditor
British Standardization Institute Management Systems        March 12  to 13 Manchester, UK Internal Auditor: ISO 13485
British Standardization Institute Management Systems     16th  March Manchester, UK Introduction to Medical Devices Management Systems - ISO 13485
The Center for Professional Innovation and Education(CFPIE) March 12 to 13 Malvern, PA USA Labeling and Labeling Controls in the Medical Device Industry
British Standardization Institute Management Systems March
17 to
 18		 Manchester, UK Internal Auditor: ISO 13485
British Standardization Institute Management Systems March
19 to
 20
 Manchester, UK Medical Device Risk Management - ISO 14971:2007
The Center for Professional Innovation and Education(CFPIE) March
23 to
 24
 Dublin, Ireland Overview Of FDA Regulatory Compliance For Medical Devices
Management Forum March
23 to
 24
 London, UK INJECTABLE DRUG DELIVERY - Devices Technology & Development
British Standardization Institute Management Systems March
23 to
 27 		Stirling, UK OH&S Management Systems Auditor/Lead Auditor (IRCA Certified)
British Standardization Institute Management Systems 30th   March
 Heathrow, UK Introduction to BS OHSAS 18001:2007
Management Forum 31st March
 London, UK AN INTRODUCTION TO POST MARKETING SURVEILLANCE AND THE EUROPEAN MEDICAL DEVICE VIGILANCE SYSTEM
British Standardization Institute Management Systems 1st March - 31st April Heathrow, UK Implementing a BS OHSAS 18001 Management System


                                    April 2009

Organizer Date Location Event
British Standardization Institute Management Systems April 02 - 03 Heathrow, UK BS OHSAS 18001 Internal Auditor
Management Forum April 02 - 03 London, UK AN INTRODUCTION TO THE MEDICAL DEVICE DIRECTIVES
British Standardization Institute Management Systems 6th April Stirling, UK Introduction to BS OHSAS 18001:2007
British Standardization Institute Management Systems April 20 - 24 York, UK OH&S Management Systems Auditor/Lead Auditor (IRCA Certified)
The Center for Professional Innovation and Education(CFPIE) April 23 - 24
Berlin, Germany
 Medical Devices: EU Directives, Guidance, CE Marking and ISO Standard Certifications
The Center for Professional Innovation and Education(CFPIE) April 23 - 24 Dublin, Ireland Overview Of FDA Regulatory Compliance For Medical Devices
Management Forum April 23 - 24 London, UK FDA MEDICAL DEVICE INSPECTIONS
The Center for Professional Innovation and Education(CFPIE) April 30th to 1st May Dublin, Ireland FDA Inspections of Clinical Data Systems



                                   May 2009

Organizer Date Location Event
British Standardization Institute Management Systems May 05 - 06 Chiswick, UK FDA - The Quality System Regulation (QSR, 21 CFR Part 820)
British Standardization Institute Management Systems 11th May Manchester, UK Introduction to Medical Devices Management Systems - ISO 13485
The Center for Professional Innovation and Education(CFPIE) May 13 - 15 Orange County, CA
USA		 Good Manufacturing Practices (cGMP)
British Standardization Institute Management Systems May 14 - 15
Manchester, UK
 Medical Device Risk Management - ISO 14971:2007
British Standardization Institute Management Systems 18th May Milton Keynes, UK Introduction to BS OHSAS 18001:2007
British Standardization Institute Management Systems May 19 - 20 Milton Keynes, UK Implementing a BS OHSAS 18001 Management System
The Center for Professional Innovation and Education(CFPIE) May 19 - 20 Malvern, PA USA Good Monitoring Practices for Medical Devices
The Center for Professional Innovation and Education(CFPIE) May 20 - 22 Berlin, Germany Reporting Failure Investigations and Process Deviations
The Center for Professional Innovation and Education(CFPIE) May 20 - 21 Orange County, CA
USA		 Auditing and Qualifying Suppliers and Vendors – An Effective Risk Based Approach
The Center for Professional Innovation and Education(CFPIE) May 21 - 22 Malvern, PA USA Medical Devices: EU Directives, Guidance, CE Marking and ISO Standard Certifications
The Center for Professional Innovation and Education(CFPIE) May 25 - 26 Berlin, Germany How to Implement Risk Management Principles and Activities Within a Quality Management System
British Standardization Institute Management Systems 26th May Cardiff, UK Introduction to BS OHSAS 18001:2007
British Standardization Institute Management Systems May 27- 28 Cardiff, UK Implementing a BS OHSAS 18001 Management System



                                   June 2009

Organizer Date Location Event
British Standardization Institute Management Systems 1st June Manchester, UK Introduction to BS OHSAS 18001:2007
British Standardization Institute Management Systems June 02 - 03 Manchester, UK Implementing a BS OHSAS 18001 Management System
British Standardization Institute Management Systems 8th June Swindon, UK Introduction to BS OHSAS 18001:2007
The Center for Professional Innovation and Education(CFPIE) June 08 - 10
Orange County, CA
USA
 Process Validation for Medical Devices
British Standardization Institute Management Systems June 08 - 12 Heathrow, UK OH&S Management Systems Auditor/Lead Auditor (IRCA Certified)
The Center for Professional Innovation and Education(CFPIE) June 15 - 16 Orange County, CA
USA		 FDA Inspections of Clinical Data Systems
The Center for Professional Innovation and Education(CFPIE) June 16 - 17 Orange County, CA
USA		 Design Control for Medical Device Professionals
The Center for Professional Innovation and Education(CFPIE) June 17 - 19 Malvern, PA USA Technical Writing for the Pharmaceutical, Medical Device, and Biotech Industries
The Center for Professional Innovation and Education(CFPIE) June 18 - 19 Orange County, CA
USA		 Design Validation, Verification, and Risk Analysis for Medical Device Professionals
The Center for Professional Innovation and Education(CFPIE) June 18 - 19 Malvern, PA USA Effective Risk-Based Applications of Drug cGMPs and Validation Req. for Cosmetics and OTC Drug Prod.
British Standardization Institute Management Systems June 22 - 26 Manchester, UK OH&S Management Systems Auditor/Lead Auditor (IRCA Certified)