Regulatory Affairs

Home :: All Courses Number of Courses: 14

Upcoming

2011
21/02/2011
2 - Day Course 		Supplier Qualification – Managing Risk in the Supply Chain
Lecturer: Ms. Karen Ginsbury
 
14/03/2011
2 - Day Course 		Marketing Authorization of Biologicals in the EU What needs to be considered
Lecturer: Dr. Barbara Jentges
 
15/03/2011
2 Meetings 		MedDRA® : A Comprehensive Training Course
Lecturer: Dr Elliot Brown
 
16/03/2011
2 - Day Course 		Building eCTD-compliant Documents and Preparing an eCTD Submission
Lecturer: Dr. Barbara Jentges
 
2010
20/10/2010
2 - Day Course 		Quality Assurance in the QC Laboratory
Lecturer: Ms. Karen Ginsbury
 
13/12/2010
2 - Day Course 		World wide regulatory affairs of medical devices
Lecturer: Ms. Shoshana Friedman
 
16/12/2010
2 - Day Course 		EU Directives & Requirements for Medical Device Marketing
Lecturer: Ms. Shoshana Friedman
 

Past Activities

2010
TBA
One Day Course 		Conducting, Documenting and Ensuring Effective Investigations
Lecturer: Ms. Karen Ginsbury
 
TBA
One Day Course 		Quality Aspects in Management of Contract Manufacturers
Lecturer: Ms. Karen Ginsbury
 
TBA
2 - Day Course 		European Drug Regulatory Affairs: Strategy and Practice with European Regulatory Procedures
Lecturer: Dr. David Jacobs
 
TBA
One Day Course 		Writing SOPs - Workshop
Lecturer: Ms. Karen Ginsbury
 
TBA
One Day Course 		System & Equipment Qualification & Validation
Lecturer: Ms. Karen Ginsbury
 
TBA
One Day Course 		Pharmacovigilance - basic level
Lecturer: Dr Irene Fermont
 
TBA
One Day Course 		Regulatory & Clinical Considerations in the Development of Combination Products
Lecturer: Ms. Barbara Fant