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Nr.DateConference/CourseLocationProgram
71678-9 February 2012Microbiology for Non-MicrobiologistsCopenhagen, DenmarkPDF-File
725014-15 February 2012Validation of Molecular Biological MethodsPrague, Czech RepublicPDF-File
722416-17 February 2012Continuous Quality ImprovementPrague, Czech RepublicPDF-File
720923-24 February 2012ICH Q8 Master Class - Efficient Use of Quality by Design ElementsBasel, SwitzerlandPDF-File
718529 February - 2 March 2012Microbiological Best Laboratory PracticesPrague, Czech RepublicPDF-File
71321-2 March 2012GMPs in Storage, Transportation and Cold ChainBerlin, GermanyPDF-File
71006-7 March 2012The new FDA/EU Approach to Process ValidationHeidelberg, GermanyPDF-File
713513-14 March 2012Change Control - New Aspects and Best PracticesBerlin, GermanyPDF-File
715413-14 March 2012Quality of Pharmaceutical Packaging Systems: From Development to Routine ControlBerlin, GermanyPDF-File
718315-16 March 2012GMP for Beginners - Understanding the importance of GMPMunich, GermanyPDF-File
717415-16 March 2012Quality Control of Raw MaterialsBerlin, GermanyPDF-File
720115-16 March 2012Handling Changes and VariationsVienna, AustriaPDF-File
722720-21 March 2012Pharmaceutical Contracts: GMP and Legal ComplianceBarcelona, SpainPDF-File
713620-21 March 2012Isolator Technology WorkhopsBasle, SwitzerlandPDF-File
723521-23 March 2012,Contamination ControlBudapest, HungaryPDF-File
714322-23 March 2012Qualified Person Education CourseBarcelona, SpainPDF-File
718627-29 March 2012Auditing a fictitious API FacilityPrague, Czech RepublicPDF-File
730327-28 March 2012,Bioassays and BioanalyticsCopenhagen, DenmarkPDF-File
730427-29 March 2012Stability Testing for Biological/Biotechnological Drug Substances and Drug ProductsCopenhagen, DenmarkPDF-File
730527-29 March 2012Bioassays and Bioanalytics & Stability Testing for Biological/Biotechnological Drug Substances and Drug ProductsCopenhagen, DenmarkPDF-File
721329-30 March 2012Improve your Quality Reviews - PQR, APR, Management ReviewBerlin, GermanyPDF-File
718429-30 March 2012Risk Management in Sterile ManufacturingHeidelberg, GermanyPDF-File
720216 – 17 April 2012Integrating Analytical Instrument Qualification and Computerised System ValidationPrague, Czech RepublicPDF-File
727917-18 April 2012Manufacture of highly potent APIsBarcelona, SpainPDF-File
718717-18 April 2012CTD, CEP and Active Substance Master FileHeidelberg, GermanyPDF-File
724417-20 April 2012Computer Validation - Introduction to Risk Management AND The GAMP®5 Approach
Save up to EUR 490,- by booking both courses!
Barcelona, SpainPDF-File
724317 April 2012Computer Validation: Introduction to Risk ManagementBarcelona, SpainPDF-File
714418-20 April 2012Computer Validation - The GAMP®5 ApproachBarcelona, SpainPDF-File
720318-20 April 2012Maximising HPLC ProductivityPrague, Czech RepublicPDF-File
720719-20 April 2012Cleaning ValidationBudapest, HungaryPDF-File
10313Monday, 23 April 2012, 14.00h – 15.30h (CET)GMP Webinar:
GMP meets GLP - a practical approach
 PDF-File
718224-26 April 2012Validation of Analytical Test Procedures and Measurement UncertaintyHeidelberg, GermanyPDF-File
725624 April 2012Pharma Congress Production & Technology 2012 - 1st DayDüsseldorf/Neuss, GermanyPDF-File
725725 April 2012Pharma Congress Production & Technology 2012 - 2nd DayDüsseldorf/Neuss, GermanyPDF-File
4000024-25 April 2012Glass - Glass Breakage - (Micro) Cracks
Part of the "Pharma Congress 2012"
Düsseldorf/Neuss, GermanyPDF-File
725524-25 April 2012Pharma Congress Production & Technology 2012 - 1st + 2nd DayDüsseldorf/Neuss, GermanyPDF-File
4000424-25 April 2012Barrier Systems Conference
Part of the "Pharma Congress 2012"
 PDF-File
728025-27 April 2012GMP for Vaccine ManufacturersBerlin, GermanyPDF-File
719025 April 2012Pre-course Session: Suppliers from China and IndiaVienna, AustriaPDF-File
719126-27 April 2012Integrated and Efficient Supplier QualificationVienna, AustriaPDF-File
719225-27 April 2012Integrated and Efficient Supplier Qualification & Pre-course Session: Suppliers from China and IndiaVienna, AustriaPDF-File
72762-3 May 2012Pharmaceutical Biotechnology for BeginnersVienna, AustriaPDF-File
72123-4 May 2012Deviation Management and CAPABarcelona, SpainPDF-File
72463-4 May 2012Pharma Engineering for Non-EngineersBudapest, HungaryPDF-File
73193-4 May 2012Statistical Process Control - A key tool for process understanding in the process validation life cycleHeidelberg, GermanyPDF-File
73027 - 8 May 2012The 3rd University of Würzburg Anti-Counterfeit Conference
Strategies against Falsified/Counterfeit Medicines
Würzburg (near Frankfurt), GermanyPDF-File
71538-9 May 2012Reference StandardsBerlin, GermanyPDF-File
73478 May 2012European Endotoxin and PyrogenTesting ConferenceFrankfurt/Main, GermanyPDF-File
73469-10 May 20125th European Microbiology ConferenceFrankfurt/Main, GermanyPDF-File
73488-10 May 2012European Endotoxin and Pyrogen Testing Conference and European Microbiology Conference
Book both conferences and save up to EUR 400,-!
Frankfurt/Main, GermanyPDF-File
727414-15 May 2012"Japan Quality"Heidelberg, GermanyPDF-File
728415-16 May 2012Efficient Batch Record ReviewPrague, Czech RepublicPDF-File
720615-16 May 2012Environmental MonitoringCopenhagen, DenmarkPDF-File
726815-16 May 2012Pre-conference workshop to the European Computer Validation ConferenceCopenhagen, DenmarkPDF-File
726915-16 May 2012European Computer Validation Conference – the new Annex 11Copenhagen, DenmarkPDF-File
727015-16 May 2012European Computer Validation Conference – the new Annex 11 + pre-conference workshopCopenhagen, DenmarkPDF-File
730621-22 May 2012Raw Data, Results and Reportable Values (Laboratory Data Integrity)Copenhagen, DenmarkPDF-File
722522-23 May 2012GMP in API Development
Requirements of ICH Q7 Chapter 19 and practical implementation
Copenhagen, DenmarkPDF-File
734422-24 May 2012Spray Drying with Full-day hands-on Spray Drying Session at HovioneLisbon, PortugalPDF-File
719822-23 May 2012Spray DryingLisbon, PortugalPDF-File
720823-25 May 2012Impurities - Special focus on genotoxic impurities and heavy metalsCopenhagen, DenmarkPDF-File
720013-15 June 2012How to Pass EU and FDA Inspections & GMP Compliance AuditsBudapest, HungaryPDF-File
721818-20 June 2012ICH Q7 Compliance for APIs Manufactured by Chemical SynthesisBerlin, GermanyPDF-File
721918-20 June 2012ICH Q7 Compliance for APIs Manufactured by Cell Culture/FermentationBerlin, GermanyPDF-File
6666719-20 June 2012OOS Forum 2012
International Launch Conference "OOS SOP"
Prague, Czech RepublicPDF-File
733919-20 June 2012Maintaining Laboratory Computer ValidationPrague, Czech RepublicPDF-File
729219 June 2012Computer Validation: Leveraging SuppliersHamburg, GermanyPDF-File
714820-22 June 2012Computer Systems Validation Master ClassHamburg, GermanyPDF-File
729319-22 June 2012Im Auftrag der European Compliance Academy
Computer Systems Validation Master Class & Leveraging SuppliersSave up to EUR 490 by booking both courses
Hamburg, GermanyPDF-File
722020-22 June 2012ICH Q7 Auditor Training CourseBerlin, GermanyPDF-File
723127-28 June 2012European GMPs and the Role of the QPBethesda, MD 20814PDF-File
729818-19 September 2012GMP/FDA Requirements for Medical DevicesHeidelberg, GermanyPDF-File
733827 – 28 September 2012GMP meets DevelopmentBerlin, GermanyPDF-File
736427-28 September 2012GMPs for Pharmaceutical ExcipientsCopenhagen, DenmarkPDF-File
72094-5 October 2012Quality by Design in Pharmaceutical Analysis Barcelona, SpainPDF-File
722110-12 October 2012ICH Q7 Auditor Training CourseBerlin, GermanyPDF-File
736016-18 October 2012The GMP LeadauditorBudapest, HungaryPDF-File
734116-17 October 2012Marketing Authorisation Procedures in the EUMunich, GermanyPDF-File
734218-19 October 2012Marketing Authorisation Procedures in the USMunich, GermanyPDF-File
734316-19 October 2012Marketing Authorisation Procedures in the EU and the USMunich, GermanyPDF-File
732924-25 October 2012ICH Q9 Training CourseVienna, AustriaPDF-File
733025-26 October 2012ICH Q10 Training CourseVienna, AustriaPDF-File
733124-26 October 2012ICH Q9 Training Course
and ICH Q10 Training Course
Save up to EUR 600,- and book both courses simultaneously!
Vienna, AustriaPDF-File
733530-31 October 2012The new FDA/EU Approach to Process ValidationBarcelona, SpainPDF-File
73188-9 November 2012SOPs: Efficient Design, Management and TrainingPrague, Czech RepublicPDF-File
736913-14 November 2012How to write the Quality Part of an IMPDVienna, AustriaPDF-File
738114-16 November 2012The Validation ManagerPrague, Czech RepublicPDF-File
719614 - 16 November 2012FDA Compliance in Analytical LaboratoriesHeidelberg, GermanyPDF-File
727715-16 November 2012GMP for Beginners - Understanding the importance of GMPPrague, Czech RepublicPDF-File
739615-16 November 2012,The GMP Compliance ManagerBudapest, HungaryPDF-File
736621-23 November 2012Computer Validation - The GAMP®5 ApproachCopenhagen, DenmarkPDF-File
736720-23 November 2012,Computer Validation - Introduction to Risk Management AND The GAMP®5 Approach
Save up to EUR 490,- by booking both courses!
Copenhagen, DenmarkPDF-File
736520 November 2012Computer Validation: Introduction to Risk ManagementCopenhagen, DenmarkPDF-File