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Number of Courses: 31

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1-Day course 19881508	Chiral Separation Lecturer: Dr. Nelu Grinberg
2-Day course 07009	Proteins & Related Materials Lecturer: Prof. Ira Krull
1-Day course 19901508	Bioassay Development and Validation - Statistical Concepts Behind Bioassay and Validation Lecturer: Dr. David Lansky
3-Day course 08014	Clinical Quality Assurance (CQA) Lecturer: Steve Schwartz
2-Day course 19791508	Applicable CAPA (Corrective Action, Preventive Action) Lecturer: Malcolm Ross
2-Day course 19811508	Management & Monitoring of Clinical Trials Lecturer: Vered Levi
1-Day course 19801508	Polymorphism - Regulatory & Analytical Aspects Lecturer: Ms. Yehudith Aronhime
1-Day Course 19841508	Validation of Analytical Methods for Proteins Lecturer: Prof. Ira Krull
3-Day Course 08177	The Analysis and Characterization of Protein Therapeutic Drugs Lecturer: Mr David Carr
1-Day course 19871508	Sterilisation by Radiation Lecturer: Mr. Martell Winters
2-Day Course 19861508	EtO - Ethylene Oxide Sterilisation : Mr. Dan Floyd
1-Day course 19981508	Sterilisation of Allograft Tissue Lecturer: Mr. Martell Winters
3-Day Course 19771508	Managing Regulatory Affairs for Medical Devices Lecturer: Shosh Friedman
2 - Day Course 08211	Preparative High Performance Liquid Chromatography Lecturer: Dr. Henri Colin, France This course is intended for production managers, chemical engineers and chemists in the pharmaceutical industry who want to understand the principles of PHPLC and some of its key features for successful applications at pilot and production levels.
2 - Day Course 08214	Quantitative Analysis by LC–MS Lecturer: Dr. Wilfried Niessen, the Netherlands One of the most important applications of LC–MS is its use in routine quantitative analysis, in preclinical and clinical studies to sustain drug development, and in food safety and environmental analysis. This two-day course pays specific attention to asp

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		Quantitative Analysis by LC–MS
		
	
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		Patient Recruitment Strategy
		
	
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		Clinical Project Management 
		
	
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		Managing Risks of Pharmaceutical Products
		
	
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		Rheology for Chemists 
		
	
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		An Introduction to CDISC (Clinical Data Interchange Standards Consortium)
		
	
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		The QC Laboratory
		
	
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		Strategic Thought - Accelerated Development of Pharmaceuticals
		
	
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		Software Validation
		
	
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		Design of Experiments for Efficient and Practical Assay Development and Validation
		
	
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		Introduction to Solid-State NMR
		
	
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		Proteins & Related Materials
		
	
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		Process Validation 
		
	
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		Structure-Related Sample Treatment
		
	
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		Quality Management Retreat
		
	
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		Pharmaceutical Packaging Technology
		
	
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		Theory, Fundamentals, Methods and Applications of Omics Technologies – Proteomics, Peptidomics, Glycomics, Metabolomics and Other Omics

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