To view the full 2011 Educational Programme please click here.

Below are forthcoming USA Educational Events. For details of in-house courses click here

Course title	Location	Start Date	No. of days	More Info	Book Online	Register Interest
November 2010
MSc Registration Fee	USA	11/03/10	0	X
February 2011
SOP and Recordkeeping for Compliance to 21 CFR 111	Salt Lake City Marriott City Center, Utah	02/10/11	1
FDA Inspection Readiness	NSF International Headquarters, Ann Arbor, Michigan	02/22/11	1
Corrective Action and Management (CAPA)	NSF International Headquarters, Ann Arbor, Michigan	02/23/11	1
March 2011
Successful EU GMP Inspection Management	Bethesda Marriott, Bethesda, MC	03/08/11	3
Meeting the Regulatory Requirements for Clinical Trials in the EU	Royal Sonesta HOtel, Boston, MA	03/15/11	2
FDA Inspection Readiness	Salt Lake City, Utah	03/15/11	1
Corrective Action and Management (CAPA)	Salt Lake City, Utah	03/16/11	1
Devising a Regulatory Submission Strategy for the EU	Royal Sonesta Hotel, Boston, MA	03/17/11	1
Human Error: Causes and Prevention	Bethesda Marriott Hotel, Washington, MD	03/29/11	3
April 2011
Module 9 Quality Management Systems	Boston	04/04/11	3
Testing Method Selection, Specification Setting and Equipment Qualification	NSF International Headquarters, Ann Arbor, Michigan	04/05/11	3
Workshop on Best Practices for CAPA Management	Royal Sonesta Hotel, Boston	04/07/11	0
Workshop on Best Practices for Deviation Investigations	Royal Sonesta Hotel, Boston	04/07/11	0
May 2011
Vendor Qualification and Audit Training	Secacus, New Jersey prior to SupplySide East	05/02/11	2
Registering Drug Products in the EU: Quality (CMC) Requirements	Bethesda Marriott Hotel, Bethesda, MA	05/10/11	3
Effective Pharmaceutical Audits and Self-Inspections	Le Meridien Cambridge, Boston	05/16/11	3
Cleaning and Control of Cross-Contamination	NSF International Headquarters, Ann Arbor, Michigan	05/24/11	1
Process Definition and Control; Facility/Utilities Design and Monitoring	NSF International Headquarters, Ann Arbor, Michigan	05/25/11	1
June 2011
21 CFR 111 Dietary Supplement GMP Overview	NSF International Headquarters, Ann Arbor, Michigan	06/07/11	2
SOP and Recordkeeping for Compliance to 21 CFR 111	NSF International Headquarters, Ann Arbor, Michigan	06/09/11	1
Pharmaceutical GMP	Le Meridien Hotel, Cambridge, Boston	06/14/11	2		X
Workshop on Laboratory GMP Requirements	Le Meridien Cambridge, Boston	06/16/11	0		X
Workshop - Investigating Out of Specification Results	Le Meridian Hotel, Cambridge, Boston	06/16/11	0		X
July 2011
Testing Method Selection, Specification Setting and Equipment Qualification	NCNPR at University of Mississippi in Oxford, Mississippi	07/12/11	3
Cleaning and Control of Cross-Contamination	Salt Lake City, Utah	07/19/11	1
Process Definition and Control; Facility/Utilities Design and Monitoring	Salt Lake City, Utah	07/20/11	1
August 2011
Module 11 Investigational Medicinal Products	Boston	08/02/11	3
September 2011
Risk Assessment and Risk Management	NCNPR at University of Mississippi in Oxford, Mississippi	09/06/11	2
Staff Recruitment and Internal Training Development	NCNPR at University of Mississippi in Oxford, Mississippi	09/20/11	3
October 2011
Module 12 The Role of the Quality Leader	Boston	10/03/11	3
Stability Program Development	Las Vegas, Nevada prior to SupplySide Wet	10/11/11	2
Regulatory Affairs in the EU - Pre and Post Approval Requirements Explained	San Francisco Marriott Fisherman's Wharf Hotel	10/11/11	3		X
International Regulatory Requirements for DS	Salt Lake City, Utah	10/18/11	2
November 2011
Module 1 Pharmaceutical Law	Boston	11/01/11	3
International Regulatory Requirements for DS	NSF International Headquarters, Ann Arbor, Michigan	11/08/11	2
Effective Quality Systems for Research and Development	Le Meridien, Cambridge, Boston	11/09/11	2		X
Supply Chain Assurance and Anti-counterfeiting	Bethseda Marriott Hotel, MD	11/15/11	3		X
December 2011
Module 2 Medicinal Chemistry	Boston	12/06/11	3