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Nr.DateTitle of Conference
115015-16 Sept. 2016ECA - Handling of Foreign Particles in APIs
114814-15 Septeber 2016ECA-Protective Packaging Systems
114707th September 2016ECA - Monocyte Activation Test - MAT
114629/30 September 2016ECA - Ambient Transport and Cold Chain
114220-21 June 2016ECA - Track & Trace Training Course
114124 June 2016ECA - Stability Testing for Biological/Biotechnological Drug Substances and Drug Products
114022-23 June 2016ECA - Bioassays and Bioanalytical Methods
113916/17 June 2016ECA - Quality Metrics to foster Continual Quality Improvement
113509-10 June 2016ECA - Quality Oversight
113410 May 2016ECA - Workshop Bioindicators
11287-8 April 2016ECA - How to implement the new GDP requirements for APIs
112715-17 March 2016ECA - GMP for Equipment, Utilities and Facilities
112609-11 March 2016Microbiological Identification Hands-on Laboratory Training Course
111904. December 2015ECA - Post Conference OOS Workshop
111505-06 November 2015ECA - Training in a GMP Environment
111421-23 June 2016ECA - Data Integrity
110817-18 November 2015ECA - The GDP-Audit
109807.-09. June 2016ECA - Pharmaceutical Packaging Systems - Development & Quality Control
109221.-22. June 2016ECA - Pharmaceutical Water
109110-11 March 2016ECA - Cloud Computing in a GxP Environment
108924-26 March 2015ECA - Protein Analytics
108815.-17. Mrz 2016ECA - GDP: How to get you there
108209. December 2014ECA - European Mycoplasma Testing Conference
107724-25 November 2014ECA - The new FDA Approach to Analytical Methods Validation of Drugs and Biopharmaceuticals
107525-26 November 2015ECA - Annex 15 Conference
107307/08 October 2015ECA - Sticking, Capping, Lamination
106702-04 December 2015ECA - OOT Forum
106614-15 October 2014ECA - How to qualify Pharmaceutical Excipients Suppliers
106529./30. September 2015ECA - Reconstruction and Upgrading of GMP Facilities
106426-27 November 2015ECA - Virtual Systems in a GxP Environment
106312-13 April 2016ECA - GMP meets Regulatory Affairs
106114-15 June 2016ECA - Continued / Ongoing Process Verification
105903 - 05 June 2014ECA - The Technical Compliance Manager
105605/06 April 2016ECA - Combination Products
105501-02 March 2016ECA - Avoiding Non-Compliance in Packaging Operations
10524-5 March 2015ECA - Managing Pharmaceutical Quality
105118-19 February 2014ECA - Electronic Laboratory Notebooks
104926.02.2014ECA - Contracting in China
10475-6 February 2014ECA - Radiopharmaceuticals Quality, Safety and GMP Requirements
103528-29 October 2015ECA - Lean GMP Systems
103222-23 October 2013ECA - The Regulatory Compliance Expert
102703-04 November 2015ECA - Reduced Sampling / Reduced Testing
102619-20 October 2015ECA - Integrating Analytical Instrument Qualification and Computerised System Validation
102520 - 21 April 2015ECA - Document Management
102419-22 April 2016ECA - Computer Validation: Introduction to Risk Management / The GAMP 5 Approach
101624 / 25 May 2016ECA - Complaint Handling and Recall Management
101528 / 29 January 2014ECA - Protective Packaging Solutions for Pharmaceutical Product Stability
101217 / 18 February 2016ECA - The Responsible Person for Good Distribution Practices (GDP)
101010-11 November 2015ECA - GMP for Beginners in sterile Manufacturing
100907/08 May 2013ECA - ICH Q11 Training Course
100827-28 May 2014ECA - Getting Approval of Generics in the EU and USA
100707 / 08 October 2015ECA - The GMP-Compliance Manager
100605-06 November 2015ECA - Tecnology and Quality of Inhalation Drug Products
100324-25 November 2015ECA - SAP - Validation and GMP Compliance
100201-02 October 2013ECA - GMP-compliant Maintenance & Calibration
10019-10 October 2012ECA - Renovation and Upgrading of Manufacturing Facilities
99913 - 15 April 2016ECA - GMP meets Development
99730 Sep - 01 Oct 2015ECA - GMP for Medical Devices
99327 - 28 JuneECA - European GMPs and the Role of the QP
99121-22 June 2012ECA - Compliance Update: EP, USP, and JP
99030-31 May 2016ECA - Design Control for Drug - Device Combination Products
98919-20 June 2012ECA - OOS Forum 2012
9887 June 2016ECA - Computer Validation: Leveraging Suppliers
98515-16 May 2012ECA - Computer Validation Conference
98224/25 March 2015ECA - Continuous Quality Improvement
98005-06 May 2015ECA - Manufacture of highly potent compounds
95908 / 09 November 2012ECA - SOPs: Efficient Design, Management and Training
93317-19 June 2015ECA - Contamination Control
93006-08 April 2016ECA - Efficient Supplier Qualification including Pre-Course: What you need to know about Suppliers in China and India
92819.-20. April 2016ECA - Cross Contamination
92314-15 February 2012ECA - Validation of Molecular Biological Methods
91820 - 22 April 2016ECA - New USP & FDA Approaches for HPLC
91724-25 May 2016ECA - Quality by Design in Pharmaceutical Analysis
91310-12 October 2012ECA - Pharma Quality Excellence
90918-20 March 2015ECA - Electronic GMP Systems
89917/18 November 2015ECA - Japan Quality
89226/27 September 2016ECA - Process Validation in the light of the revised Annex 15 and FDA-Requirements
88821-22 May 2014ECA - Quality of Pharmaceutical Packaging Systems: From Development to Routine Control
88624. - 25. June 2015ECA - Pharmaceutical Biotechnology for Non-Biotechnologists
87829./30. September 2015ECA - GMP meets GDP
87326/27 April 2016ECA - Leachables & Extractables - Testing & Assessment
87026-27 November 2013ECA - Plastic Packaging Materials (Pharma Packaging Conference 2013)
86815 - 16 October 201ECA - GMP and GDP for Pharmaceutical Excipients
86416-19 October 2012ECA - Marketing Authorisation Procedures in the EU and US
8368-9 March 2016ECA - GMP for Beginners
83118 - 19 January 2012ECA - Medical Devices Validation Manager
83010-11 December 2014ECA - Rapid Microbiological Methods Conference
82705 May 2015ECA - European Microbiological OOS/OOL Workshop
82426-27 May 2014ECA - Strategies against Falsified / Counterfeit Medicines
81725-26 November 2013ECA - Printed Packaging Materials (Pharma Packaging Conference 2013)
81528-29 October 2015ECA - GMP for Vaccine Manufacturers
79918/19 February 2016ECA - Statistical Process Control - a key tool for process understanding in the process validation life cycle
79318-19 September 2012ECA - IT System and Data Security
79202 / 03 June 2016ECA - Deviation Management and CAPA
78819-20 April 2016ECA - Efficient Batch Record Desing and Review
78418/19 February 2016ECA - Pharmaceutical Contracts GMP and Legal Compliance
78023-24 June 2016ECA - Practical Statistical Tools for Analytical Laboratories
7583-4 May 2012ECA - Pharma Engineering for Non-Engineers
75307/09 October 2014ECA - GMP meets GCP Management, Supply and Quality Assurance of Clinical Trials
73611-12 February 2016ECA - Cleaning Validation
72123 -24 February 2016ECA - Virus and TSE Safety made simple
72014-15 May 2014ECA - Risk Management in Sterile Manufacturing
71617-19 March 2015ECA - Microbiological Best Laboratory Practices
71112-14 October 2016ECA - Computer Validation: Maintaining Control of Operation
6957-8 May 2015ECA - Process Simulation / Media Fill
6778-10 June 2016ECA - Computer Systems Validation Master Class
6764-5 February 2016ECA - Quality Control of Raw Materials
67519/20 November 2015ECA - ICH Q10 Training Course
67418/19 November 2015ECA - ICH Q9 Training Course
63118-20 September 2012ECA - Protein Analysis Technologies
5613-4 May 2016ECA - QP Education Course
55914-16 June 2016ECA - The Impurities Workshop
55414-16 May 2013ECA - Reference Standards
54301/02 June 2016ECA - Dissolution Testing
53927/28 October 2015ECA - Isolator Technology Workshop
53704-06 April 2016ECA - Analytical Instrument Qualification
48805-06 May 2015ECA - Environmental Monitoring
48211-12 March 2014ECA - OOS Training Course
45801/02 March 2016ECA - CTD, CEP and Active Substance Master File / Quality of Drug Substance
44114/16 March 2016ECA - ICH Q7 Compliance for APIs Manufactured by Cell Culture/Fermentation
44014/16 March 2016ECA - ICH Q7 Compliance for APIs Manufactured by Chemical Synthesis
43104/05 June 2013ECA - GMP in API Development
42307-09 June 2016ECA - Spray Drying - Solutions for Pharmaceutical Industry
39807/08 June 2016ECA - Microbiology for Non-Microbiologists
39319-21 April 2016ECA - Validation of Analytical Test Procedures and Measurement Uncertainty
38018 - 20 April 2012ECA - Maximising HPLC Productivity
32321-23 October 2015ECA - FDA-Compliance in Analytical Laboratories
23223. - 25. September 2015ECA - Inspection Management (How to pass EU and FDA Inspections)

 GMP Conferences by Topics
 Quality Assurance
 GMP in Biotechnology
 Microbiology
 Regulatory Affairs
 GMP in Pharmaceutical Development
 Quality Control
 Storage, Distribution, Transportation
 Sterile / Aseptic Manufacturing
 Computer Validation
 Technical Operations
 GMP for APIs and Excipients
 Validation
 Medical Devices
 GMP Basic Training Courses
 Packaging