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Nr.DateTitle of Conference
102007 / 08 May 2013ECA - Particles in Parenterals
101909./10.04.2013ECA - Blood, Blood Products and Plasma (conference folder NOT for sale)
101621 / 22 March 2013ECA - Complaint Handling and Product Recall
101526 / 27 February 2013ECA - Barrier Packaging
101207 / 08 May 2013ECA - The Responsible for Good Distribution Practices (GDP)
101028./29. November 2012ECA - GMP for Beginners in sterile Manufacturing
100920/21 November 2012ECA - ICH Q11 Training Course
100815-16 November 2012ECA - Getting Approval of Generics in the EU and USA
100715 / 16 November 2012ECA - The GMP-Compliance Manager
100607 - 08 November 2012ECA - Quality of Inhalation Drug Products
100530-31 October 2012ECA - Innovation Excellence Ordner steht nicht zum Verkauf!
100330-31 October 2012ECA - SAP: GMP Compliance and Validation
10029-10 October 2012ECA - GMP-compliant Maintenance & Calibration
10019-10 October 2012ECA - Renovation and Upgrading of Manufacturing Facilities
99915 / 16 May 2013ECA GMP meets Development
99718-19 September 2012ECA - GMP for Medical Devices
99626-27 September 2012ECA - QbD / PAT Conference 2012
99327 - 28 JuneECA - European GMPs and the Role of the QP
99121-22 June 2012ECA - Compliance Update: EP, USP, and JP
99025-26 June 2012ECA - Design Control for Drug - Device Combination Products
98919-20 June 2012ECA - OOS Forum 2012
98819 June 2012ECA - Computer Validation: Leveraging Suppliers
98515-16 May 2012ECA - Computer Validation Conference
98214-15 March 2013ECA - Continuous Quality Improvement
98127/29 March 2012ECA - Auditing a fictitious API Facility (Binder not for sale!)
98017-18 April 2012ECA - Manufacture of highly potent APIs
97827-29 March 2012ECA - Bioassays and Bioanalytics & Stability Testing NOT FOR SALE
96913-14 November 2012ECA - How to write the Quality Part of an IMPD (Conference folder is not available)
967 ECA - Vaccines and Biologics Development, Scale Up and Manufacturing
96615-16 November 2011ECA - Modern Sterile Facilities 2011
96408/09 November 2011ECA - Industrial Pharmacy for Non-Pharmacists
95908 / 09 November 2012ECA - SOPs: Efficient Design, Management and Training
95805 - 06 October 2011ECA - The New Pharma Directive
9565-7 October 2011ECA - QbD / PAT Conference 2011 (Conference folder is not available)
95316 - 18 October 2012ECA - The GMP Leadauditor (not for sale)
94814-15 May 2013ECA - Raw Data, Results and Reportable Values
94319-20 May 2011ECA - 4th European GMP Conference Binder not for sale!
93816/17 April 2013ECA - ICH Q8 Master Class
9375-6 May 2011ECA - New EU GMP Annex 11 Regulations for computerised Systems
9362-4 May 2011ECA - Computerised Systems in analytical Laboratories
93321-23 March 2012ECA - Contamination Control
93010/12 April 2013ECA - Integrated and Efficient Supplier Qualification including Pre-Course: What you need to know about Suppliers in China and India
92815 / 16 March 2011ECA - Cross Contamination
92314-15 February 2012ECA - Validation of Molecular Biological Methods
91812 - 13 October 2011ECA - An Introduction to HPLC in Analytical GMP Laboratories
91704/05 October 2012ECA - Quality by Design in Pharmaceutical Analysis
91426 / 27 Octobre 2010ECA - Microbiological Culture Media
91310-12 October 2012ECA - Pharma Quality Excellence
91114-15 October 2010ECA - GMP- compliant Lyophilisation - with Plant Tour at Cilag AG
90929-31 January 2013ECA - Electronic GMP Systems
90629 September - 01 October 2010ECA - QbD / PAT Conference 2010 (Conference folder is not available)
90221-22 June 2010ECA - Ensuring Analytical Control Laboratory Compliance with FDA & USP Requirements
90116-17 June 2010ECA - 2nd Conference on Tracking & Tracing
90020-21 October 2011ECA - Best Practices for Auditing GMP Laboratories (Conference folder is not available)
89914./15. May 2012ECA - Japan Quality
894 ECA - Bio Production Forum - Fill and Finish for Biopharmaceuticals - The conference folder is not available-
89223/24 April 2013ECA - The new FDA/EU Approach to Process Validation
89018-20 May 2010ECA - Handling of highly potent Compounds
88813-14 March 2012ECA - Quality of Pharmaceutical Packaging Systems: From Development to Routine Control
88619/20 March 2013ECA - Pharmaceutical Biotechnology for Beginners
88424-25 May 2011ECA - Visual Inspection Systems
87814-15 February 2013ECA - GMP meets GDP
87304/05 December 2012ECA - Leachables & Extractables - Testing & Assessment
87029-30 November 2012ECA - Plastic Packaging Materials (Pharma packaging Conference 29-30 November 2012)
86827 - 28 September 2012ECA - GMPs for Pharmaceutical Excipients
866 ECA - GMP Compliance for Biopharmaceuticals and Workshop GMP and Adavanced Therapy Medicinal Products (Folder not for sale)
86416-19 October 2012ECA - Marketing Authorisation Procedures in the EU and US
86220/21 September 2011ECA - GMP- and FDA-Compliance in Pharmaceutical Development and IMP Manufacturing
86118-19 October 2011ECA - Efficient and Effective Quality Management in the Analytical Laboratory (Conference folder is not available)
85827-28 September 2011ECA - Failure Investigation and CAPA in Sterile Manufacturing
85518 May 2010ECA - Measurement Uncertainty
84818/19 May 2010ECA - Good Development Practice Part 1: Quality by Design & Efficiency in Pharmaceutica Development
83618-19 April 2013ECA - GMP for Beginners
83507 - 08 May 2013ECA - Change Control (Conference folder is not available)
83118 - 19 January 2012ECA - Medical Devices Validation Manager
83011-12 December 2012ECA - Rapid Microbiological Methods Conference
82723 April 2013ECA - European Mycoplasma Testing Conference
8247-8 May 2012ECA - Strategies against Falsified / Counterfeit Medicines (Conference Folder is not available)
82107 / 08 November 2011ECA - Analytical Data - Interpretation and Treatment
81728-29 November 2012ECA - Printed Packaging Materials (Pharma Packaging Conference 2012 - 28-29 November 2012)
81525-27 April 2012ECA - GMP for Vaccine Manufacturers
80920/22 February 2013ECA - ICH Q7 Auditor Training Course (The conference folder is not available)
79918 / 19 April 2013ECA - Statistical Process Control - a key tool for process understanding in the process validation life cycle
79318-19 September 2012ECA - IT System and Data Security
79203 / 04 May 2012ECA Deviation Management and CAPA
78924/25 April 2013ECA - European Microbiology Conference
78815-16 May 2012ECA - Efficient Batch Record Review
78419/20 March 2013ECA - Pharmaceutical Contracts GMP and Legal Compliance
78016 - 17 May 2013ECA - Practical Statistical Tools for Analytical Laboratories
7583-4 May 2012ECA - Pharma Engineering for Non-Engineers
75328/30 November 2012ECA - GMP meets GCP Management, Supply and Quality Assurance of Clinical Trials
74430 June 2011ECA - Out of Specification Results Post - course Workshop on Failure Investigation
73611-12 April 2013ECA - Cleaning Validation
73510-11 October 2011ECA - The Pharmaceutical Laboratory Manager
72319/20 May 2010ECA - Good Development Practice Part 2: Formulation Development & Manufacturing of Paediatric Drugs
72130 -31 October 2012ECA - Virus and TSE Safety made simple
72029-30 March 2012ECA - Risk Management in Sterile Manufacturing
71918-19 March 2010ECA - Efficient Supplier Qualification
716 ECA - Microbiological Best Laboratory Practices
71120-21 September 2012ECA - Computer Validation: Maintaining Control of Operation
70324 / 25 November 2011ECA - The GMP-Compliance Manager
6957-8 October 2010ECA - Process Simulation / Media Fill
67720-22 June 2012ECA - Computer Systems Validation Masterclass
67628 February - -1 March 2013ECA - Quality Control of Raw Materials
67525/26 October 2012ECA - ICH Q10 Training Course
67424/25 Oktober 2012ECA - ICH Q9 Training Course
67114 - 16 November 2012ECA - The Validation Manager
63226 - 28 November 2012ECA - Setting Specification and Stability Testing
63118-20 September 2012ECA - Protein Analysis Technologies
62408 / 09 February 2011ECA - Elastomeric Closures for Injections
59016 April 2013ECA - Computer Validation: Introduction to Risk Management
56127-28 February 2013ECA - QP Education Course
55923-25 May 2012ECA - Impurities Detecting, Identifying, Quantifying, Specifying and Reporting
55414-16 May 2013ECA - Reference Standards
54317/19 October 2012ECA - Dissolution Testing
53920/21 March 2012ECA - Isolator Technology Workshop
53720 - 22 February 2013ECA - Analytical Instrument Qualification
4887.-8. May 2013ECA - Environmental Monitoring
48209.-10. April 2013ECA - OOS Training Course
45819/20 March 2013ECA - CTD, CEP and Active Substance Master File / Quality of Drug Substance
44118/20 February 2013ECA - ICH Q7 Compliance for APIs Manufactured by Cell Culture/Fermentation
44018/20 February 2013ECA - ICH Q7 Compliance for APIs Manufactured by Chemical Synthesis
43104/05 June 2013ECA - GMP in API Development
42322 - 24 May 2012ECA - Spray Drying - Solutions for Pharmaceutical Industry
39805/06 February 2013ECA - Microbiology for Non-Microbiologists
39305-07 March 2013ECA - Validation of Analytical Test Procedures and Measurement Uncertainty
38018 - 20 April 2012ECA - Maximising HPLC Productivity
34717-19 April 2013ECA - Computer Validation - The GAMP5 Approach
32314-16 November 2012ECA - FDA-Compliance in Analytical Laboratories
29506 - 07 October 2011ECA - Stability Testing for Drug Substances and Drug Products
232 ECA - How to Pass EU and FDA Inspections and GMP Compliance Audits
21607 - 09 June 2011ECA - The Pharma Engineer