The ISPE 2010 Washington Conference brings together all levels of pharmaceutical industry professionals to network and benefit from a variety of seminars and trainings. Washington Conference features practical applications, results orientated workshops, and a special FDA-ISPE collaboration on Pharma Quality Systems.
Seminars
7-8 June
- Barrier Isolation Technology Forum: Innovation, Updates, and New Case Studies (E01)
- PQLI®: Case Studies in QbD for Biotechnology and Small Molecule Product Realization (E02)
- Science and Risk-Based Commissioning and Qualification: Transitioning and Transforming (E03)
- Critical Utilities: Best Practices in Managing Risk and Cost (E04)
8 June
- GAMP® Good Practice Guide: Manufacturing Execution Systems – Guide Launch (D01)
- Practical Answers to Common HVAC Questions – An introduction to the HVAC Good Practice Guide (F01)(Free to all ISPE Members and 2010 Washington Conference Attendees)
9-10 June
- Science and Risk-based Validation: Practical Approaches Across Projects by Breaking Down Implementation Silos (E05)
- FDA-ISPE Collaboration: Pharmaceutical Quality Systems (E06)
- GAMP® Good Practice Guide: A Risk-Based Approach to Operation of GxP Computerized Systems (E07)
- Sustainability: Best Practice Case Studies and Legislation Impact (E08)
- Trends in Biologics Manufacturing (with MedImmune Tour of Therapeutic Protein facility) (E09)
Training Courses
7-8 June
- Process Validation in Biotechnology Manufacturing (T32) – Advanced
- Cleaning Validation Principles (T17) – Intermediate
Register on or before 10 May to receive early bird pricing.
Related posts:
- ISPE Brussels Conference 2010 on Risk-based control strategies in pharmaceutical industry
- ISPE offering online learning course on USFDA GMP
- Risk-MaPP: What is it and Why You Need it!
- Process Validation in Manufacturing Biopharmaceuticals
- Australian code of good manufacturing practice for medicinal products
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