Analytical section
Duphar, 1986.
Particle size analysis.
Analytical section
Duphar, 1987.
Particle characterisation.
Formulation Development, Chemical Development and Chemical Technology Departments
Duphar, 1988.
Particle size analysis of pharmaceuticals, pesticides and LC stationary phases.
Syllabus PAON-cursus "Particle Size Measurement", 1989. Veldhoven (PAON).
Validation of chromatography methods in bioanalysis.
Analytical section
Duphar, April 1991.
Method validation.
DARQA
Zeist, May 1997.
Bioanalysis in general.
Students Biomedical Sciences
Solvay, October 1998.
Contracting Out.
Pharmaceutical Analysis and Development Departments
Solvay, October 1998.
Validation bioanalysis for toxicokinetics.
BioAnalysis en Drug Safety Departments
Solvay, November 1998.
Bioanalysis and Pharmacokinetics
Students Biomedical Sciences
Solvay, October 1999.
Bioanalysis and Pharmacokinetics
Students Biomedical Sciences
Solvay, October 2000.
Quality systems in bioanalysis
PhD Students Pharmacy & Medicine
Solvay, June 2001
Bioanalysis: General overview
Scientific Exchange: Pharmacology, Drug Safety, BioAnalysis
Solvay, November 2001
Quality systems in bioanalysis
PhD Students Pharmacy & Medicine
Solvay Pharmaceuticls, May 2002
Gewinnung von Proben: Stabilität während Plasma-/Serumgewinnung (Sampling: stability during plasma-/serum collection)
A&M Workshop 2004: Biovalidierung nach “Shah”. Unsetzung der FDA “Guidance for Industry”
Bedburg-Kaster, Germany, May 2004
Outsourcing: Challenges & Successes
3rd Annual Bioanalysis in Clinical Research
Olympia Conference Centre, London, UK, February 2008
EBF: ISR – MIST – EMEA
3rd Calibration and Validation Group Workshop on Recent Issues in Regulated Bioanalysis
Calibration and Validation Group, Montreal, Canada, April 2009
EBF survey: Quality systems in macromolecule analysis
2009 AAPS National Biotechnology Conference
Seattle, WA, USA, June 2009
EBF Perspective on the New EMA Guidelines on Bioanalytical Method Validation (BMV) and input on global BMV harmonization
The 4th Workshop on Recent Issues in Regulated Bioanalysis of the Canadian LC-MS/MS group (CVG)
Montreal, QC, Canada, April 2010
New EBF organsiation and how CROs may fit in there
EBF-CRO meeting
Brussels, Belgium, October 2010
Building the Global Bioanalysis Consortium – Working towards a functional globally acceptable and harmonized guideline on bioanalytical method validation
2010 FABIAN meeting “Doping opnieuw geanalyseerd”
Utrecht, Netherlands, November 2010
Update on EBF organisation
EBF 3rd open meeting “From Challenges to Solutions”
Barcelona, Spain, December 2010
Building the Global Bioanalysis Consortium – Working towards a functional globally acceptable and harmonized guideline on bioanalytical method validation
SoFAQ International Seminar – Quality Assurance and Electronic Data
Paris, France, December 2010
Learning From Issues in Assay Cross-Validation / Method Transfers
The 5th Bioanalysis Workshop (CVG)
Montreal, Canada, April 2011
How to Implement the EMA Guideline on Bioanalytical Method Validation
EBF 4th open symposium “Less is More”
Barcelona, Spain, November 2011
The EMA Bioanalytical Method Validation Guideline: process, history, discussions and evaluation of its content.
JBF 2nd Symposium
Tokyo, Japan, March 2012
Historic perspective on the evolution of Regulated Bioanalysis
Acbio 1st Bioanalytical Symposium
Sao Paulo, Brazil, May 2012
The EMA Bioanalytical Method Validation Guideline: process, history, discussions and evaluation of its content.
Acbio 1st Bioanalytical Symposium
Sao Paulo, Brazil, May 2012
Feedback from GBC Harmonization team leaders Face to Face (March 2012)
EBF 3rd Focus Meeting “Hatching”
Brussels, Belgium, June 2012
The EMA Bioanalytical Method Validation Guideline: process, history, discussions and evaluation of its content.
EBF 5th Open Symposium “Old Battles, New Horizons”
Barcelona, Spain, November 2012
Global Regulatory Issues: one BA method, one validation, one report …
14th Land O’Lakes Bioanalytical Conference
Madison WI, USA, July 2013
Global Regulatory Issues: one BA method, one validation, one report …
BioanalysisZone Expert Panel Presentations
http://www.bioanalysis-zone.com/media-centre/land-o-lakes-global-regulatory-issues-peter-van-amsterdam-abbott
Global Regulatory Issues: one BA method, one validation, one report …
International Reid Bioanalytical Forum
Guildford, United Kingdom, September 2013
Successful treatment of maldigestion due to Pancreatic Exocrine Insufficiency: diagnosis, clinical picture and the challenges of measurements involved
EBF 6th Open Symposium “Moving forward together”
Barcelona, Spain, November 2013
Lab manuals for PK sampling: a Study Monitor perspective
EBF Focus Workshop “Standardised Lab Manual for bioanalytical support in clinical studies”
Brussels, Belgium, February 2014
Evaluating EMA and FDA guidance on bioanalytical method validation
10th Bioavailability / Bioequivalence, Dissolution and Biowaivers
Budapest, Hungary, April 2014
Introduction to the CTA & NDA process in China
EBF/CBF China Days
Berlin, Germany, September 2014
GCP meets GLP – The sponsor’s perspective
DARQA Theme Day “GCP meets GLP”
Utrecht, Netherlands, January 2015
All for one, one for all - The Chinese guideline in perspective to other guidelines
CPSA Shanghai 2015 “Connecting the dots”
Shanghai, China, April 2015
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