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Nr. Date Title of Conference

793 8-9 May 2008 ECA - Current GMP Requirements on IT and Data Security

792 20 - 21 May 2008 Deviation Management and CAPA

789 22/23 April 2008 ECA - First European Microbiology Conference

784 03/04 April 2008 ECA - Pharmaceutical Contracts GMP and Legal Compliance

780 14 / 15 April 2008 Integrating Analytical Equipment Qualification and Computerized System Validation

763 28-30 November 2007 Bio Production Forum – Fill & Finish for Biopharmaceuticals

762 6-7 December 2007 ECA - Pharmaceutical Sourcing Conference

758 ECA - Pharmaceutical Engineering for Non-Engineers

757 13-14 November 2007 ECA-Process Excellence and Six Sigma in the pharmaceutical Industry

753 15-16 November 2007 ECA - The Management of Clinical Trials - GMP meets GCP

752 CV 15 Backup - Archivierung - Datenmigration im GMP-Umfeld

751 24-26 October 2007 The Heidelberg PAT Conference 2007 (Conference Folder is not available)

749 22 / 23 October 2007 GMP and FDA compliant Quality and Documentation Systems

744 04 April 2008 ECA - Out of Specification Results Post - course Workshop on Failure Investigation (Conference Folder is not available)

743 02-04 July 2008 ECA - Integrating LIMS with CDS

742 19 - 20 June 2007 ECA - Good Distribution Practice and Cold Chain Management

741 25-26 June 2007 2nd European GMP Conference (Conference Folder is not available)

739 18 / 19 June 2007 Integrating Analytical Equipment Qualification and Computerized System Validation

738 20 - 22 June 2007 ECA - Microbiological Safety for Biopharmaceuticals

736 27-28 May 2008 ECA - Cleaning Validation

735 9-10 June 2008 ECA - The Pharmaceutical Laboratory Manager

731 13/14 June 2007 Pre-filled Syringes

723 18/19 April 2007 ECA - Good Development Practice Part 2: Analytical Development and Release of IMPs

722 22/23 April 2008 ECA-Good Development Practice PART 1 Pharmaceutical Development & IMP Manufacturing

721 28 -29 April 2008 ECA - Virus and TSE Safety made simple

720 06/07 February 2008 ECA - Risk Management for Sterile Manufacturing

719 6-7 March 2008 ECA - Efficient Supplier Qualification

716 13-15 Februar 2008 ECA - Microbiological Best Laboratory Practices

711 15 - 16 March 2007 ECA - Maintaining the Validated State

704 7 - 8 December 2006 Aseptic Processing for Biopharmaceuticals

703 14-15 December 2006 ECA - Documentation Systems in Quality Assurance

702 22 - 23 November 2007 2nd QP FORUM

698 13 / 14 November 2007 ECA - Herbal Medicinal Products in Europe - Harmonization Achieved?

695 20-21 November 2006 ECA - Process Simulation / Media Fill

693 26-27 June 2007 ECA - Product Quality Review

689 27-29 September 2006 The Heidelberg PAT Conference 2006 (Conference Folder is not available)

678 26-27 June 2006 ECA - Printed Packaging Materials

677 14-16 May 2008 ECA - Computer Systems Validation Masterclass

676 11- 12 June 2008 ECA - Quality Control of Raw Materials (APIs and Excipients)

674 12/13 March 2008 ECA - ICH Q9 Training Course

673 15 - 17 May 2006 ECA - GMP-compliant Development of Biopharmaceuticals

671 05-07 March 2008 ECA - The Validation Manager

666 9-10 May 2006 ECA - Containment

664 29-31 March 2006 Microbial QC Testing - Reconcile Compliance with Efficiency

661 23 / 24 March 2006 ECA - Alternative Pyrogen Testing

658 9-10 March 2006 Recent FDA/EU Requirements on Laboratory Computers and Records

654 7-8 March 2006 IT Infrastructure Compliance and Control

652 7-8 March 2006 Maintaining the Validated State

650 04 / 05 March 2008 ECA - Quality Control and Quality Assurance of Pharmaceutical Packaging Materials

639 16-18 Januar 2006 ECA - The Paperless Laboratory

635 30 November - 1 December 2006 ECA - GC in Pharmaceutical GMP-Laboratories

632 26 - 27 November 2007 ECA - Setting Specification and Acceptance Criteria (Conference Folder is not available)

631 26/27 February 2008 ECA - Protein Analytical Technologies Bringing Copmliance and Science Together

624 13 / 14 February 2007 Elastomeric Closures for Injections

623 22/23 May 2007 ECA - Pharmaceutical Water Systems - Key Compliance Issues

622 28 October 2005 ECA - Infrastructure Library in a Regulated Environment

621 27. Oktober 2005 ECA - ITIL Service Management with ITIL

617 13/14 March 2008 ECA - ICH Q10 Training Course

612 10 - 12 June 2008 ECA - Cleanrooms FDA- and GMP-compliant design, layout and operation

608 6-7 December 2007 ECA - Microbial Contamination

607 23 September 2005 Post-Course Workshop on the Validation of Chromatography Data Systems (CDS)

604 14 / 15 September 2005 Fill and Finish for Biopharmaceuticals

603 29 - 30 September 2005 ECA - Complying with the New FDA Aseptic Guide

602 12 September 2005 NIR Conference 2005 - Pre-Conference Workshop on PAT

601 13-14 September 2005 NIR Conference 2005 Near InfraRed Spectroscopy to the Pharmaceutical Industry

599 7/8 July 2005 ECA - Modern API Facilities

598 21 June 2005 ECA - ICH Q 9 Risk Management

597 20 June 2005 The GMP Conference International GMP Hamonisation

592 21 June 2005 ECA - ICH Q8 - Pharmaceutical Development

591 22/24 June 2005 ECA - GMP Compliance for Biopharmaceuticals From Development to Production

590 8 - 9 May 2006 ECA - The Risk-based Approach to Computer Validation

580 13/14 April 2005 ECA - GMP Requirements on Cleaning and Disinfection Management

572 25-26 January 2006 ECA - PAT in Microbial QC Unit 1: Rapid Methods

567 27-28 January 2005 Process Analytical Technology (PAT)

566 26-27 January 2005 FDA's New Quality Systems and Risk Approach

563 3-4 December 2007 ECA - FDA-/GMP-compliant Extractables and Leachables Testing

561 21-22 Fevruary 2008 QP Education Course

559 27/28 May 2008 ECA - Impurities Detecting, Identifying, Quantifying, Specifying and Reporting

557 9-10 December2004 ECA - Containment Facilities

555 8 December 2004 ECA - Pharmaceutical Facilities 2004

554 29 - 30 November 2007 ECA - Reference Standards

553 17-18 November 2004 ECA - Capillary Electrophoresis

552 4-5 November 2004 ECA - Fundamental Assays in the Quality Control of Recombinant Proteins

548 12-14 October 2005 8th APIC/CEFIC European Conference on Active Pharmaceutical Ingredients

543 27/29 June 2007 ECA - Dissolution Testing

539 16-17 October 2007 ECA - Validation of Isolators

537 19 - 21 September 2007 ECA - Lab Equipment Qualification

536 15-17 June 2004 Project Management in the Pharmaceutical Industry

531 12 - 13 May 2004 Records, Risks and Regulations

530 16-17 November 2004 Process Simulation

527 05/06 November 2007 Analytical Data - Interpretation and Treatment

525 31 March - 1 April 2004 ECA - Validation of Process Control Systems

520 10-11March 2004 ECA- SAP R/3: Validation Strategies and Part 11 Implementation

516 23 - 25 November 2005 ECA - Microbiological Challenges for GMP/FDA Compliance - Masterclass -

506 18/19 October 2004 ECA - Sterile Manufacturing - GMP/FDA compliant Qualification and Validation

488 5-6 June 2008 ECA - Environmental Monitoring

482 02 - 03 April 2008 ECA - Out of Specification Results (Conference Folder is not available)

476 17-18 June2004 ECA - FDA and EU-GMPCompliance for Equipment Design

458 10/11 June 2008 ECA - CTD, CEP and Active Substance Master File / Quality of Drug Substance

441 25/27 February 2008 ECA - ICH Q7 Compliance for APIs Manufactured by Cell Culture/Fermentation

440 25/27 February 2008 ECA - ICH Q7 Compliance for APIs Manufactured by Chemical Synthesis

437 21-23 January 2004 ECA - Computerised Systems in QC and R&D Laboratories

435 2-3 December 2002 FDA and EU Compliant Raw Data Management and Archiving

434 2-5 December 2002 ECA - How to do Validation in API Production? Equipment Qualification/Process Validation/Cleaning and Cleaning Validation

431 01/02 April 2008 ECA - Chapter 19 ICH Q7A: APIs for Use in Clinical Trials What is required in Process and Analytical Development

430 13-15 November 2002 5th CEFIC/APIC European Conference on Active Pharmaceutical Ingredients

425 26-27 November 2002 ECA - Application and Validation of Bioanalytical Methods

424 18-19 November 2004 ECA - European Aseptic Conference 2004

423 10-11October 2007 ECA - Spray Drying

421 20-21 November 2002 ECA - Part 11 Conference

420 20 November 2002 Interactive Half Day Pre-Conference Workshop Part 11- Conference

412 16 - 17 February 2005 ECA - Bioindicators Current GMP Requirements on the Use of BIs

409 09/10 November 2004 ECA - EU-GMP and FDA Compliance in Pharmaceutical Development

400 19 - 20 June 2002 ECA - Electronic Records / Electronic Signatures Implementation of 21 CRF Part 11

398 22/23 November 2007 ECA - Microbiology for Non-Microbiologists

393 20 - 22 March 2007 ECA - Validation of Analytical Test Procedures

381 14 - 15 June 2004 ECA - FDA and EU-GMP Compliance for Water Systems

380 16 - 18 April 2008 Maximising HPLC Productivity

372 6 - 8 March 2002 ECA - GMP Compliance for Batch Documentation in the Pharmaceutical and API Production

364 19-20 February 2002 SAP R / 3 Validation and Part 11 Implementation

361 20 - 22 April 2005 ECA - Validation of Microbiological Test Procedures

347 23 - 25 April 2008 ECA - Computer Validation

337 14-15 June 2004 ECA - FDA and EU-GMP Compliance for Cleanrooms

323 07-09 November 2007 ECA - FDA-Compliance in Analytical Laboratories

310 8-9 October 2002 ECA - FDA-/GMP-Compliant Design of Equipment

295 27/28 November 2008 ECA - Stability Testing for Drug Substances and Drug Products

232 28-30 April 2008 ECA - How to Pass EU and FDA Inspections - GMP Compliance Auditor

216 31 May - 3 June 2005 ECA - Pharmaceutical Engineering

206 23-25 November 2005 ECA - GMP and FDA Compliance in Quality Assurance Units