Conference HomeEducation Sessions
Emerging Markets – Learn how to achieve the most from GMP operations in emerging markets.
- 104: Manufacturing Facility Design for Global Organizations
- 204: Practical Experiences of Manufacturing Projects in Emerging Markets
- 404: Latin America Regulatory Compliance Forum
- 504: Applications of Technology in Emerging Markets
Facilities and Equipment – Improve operations and design with fast-track techniques.
- 101: Case Study of a Greenfield Site’s Positive FDA-PAI Experience with Maintenance and Reliability
- 102: Re-Tasking Existing Equipment and Legacy Facilities
- 201: Build a Biotech Facility: Real Time Value Management Decision-Making Workshop (Part 1)
- 202: FOYA 2012 Winners (Part 1)
- 209: Reducing Cost Through Sustainable Initiatives (Part 1)
- 301: Build a Biotech Facility: Real Time Value Management Decision-Making Workshop (Part 2)
- 302: FOYA 2012 Winners (Part 2)
- 304: Biotech's 4th Decade: Strategies for Development and Operation of Successful Facilities
- 309: Reducing Cost Through Sustainable Initiatives (Part 2)
- 401: Practical Application of C&Q Applied Risk Management
- 402: Ultra Violet Applications and Dose Calculation for Pharma Water Treatment
- 501: Facility of the Future: Impact of Innovative Technology and Continuous Manufacturing
- 502: Improving Pharmaceutical Water Systems: A Green Approach to Water Savings - Evolution and Optimization of a High Purity Water System for Bioprocess Operations
Investigational Products – Comprehensive program for professionals engaged in manufacture and supply of materials for clinical investigation.
- 7001: Transforming your Clinical Supply Chain: Finding Your Golden Gate (Part 1)
- 7002: Transforming your Clinical Supply Chain: Finding Your Golden Gate (Part 2)
- 7003: Transforming your Clinical Supply Chain: Finding Your Golden Gate (Part 3)
- 7004: Transforming your Clinical Supply Chain: Finding Your Golden Gate (Part 4)
- 7005: Transforming your Clinical Supply Chain: Finding Your Golden Gate (Part 5)
Manufacturing Operations – Develop and manage effective contract manufacturer and supplier partnerships.
- 105: The Challenges Facing Disposable Technology and Their Solutions
- 107: Back to Basics: Good Documentation to Facilitate Compliance and Electronic Batch Record Implementation
- 205: GAMP® Part 1 – Information Security in a Global Market
- 305: GAMP® Part 2 – The Regulatory Focus on Data Integrity
- 405: Better Practices in Developing Effective Contract Manufacturer and Supplier Partnerships
- 409: Bridging the Compliance and Operational Excellence Gap
- 505: Continuous Processing and Process Control: Improving Manufacturing Through Innovation
Project Management – Find the most effective and efficient way to manage your product lifecycle.
- 108: Project Initiation and Business Case Development (Part 1)
- 208: Early Phase Project Planning for Process/Product Development Projects (Part 2)
- 308: Design Management in the Capital Project Lifecycle (Part 3)
- 408: Project Implementation of IT Infrastructure Projects (Part 4)
- 508: Managing Project Closeout, Product Approval, Product Launch (Part 5)
Regulatory
- 103: C&Q Risk Task Team Forum IV
- 109: NIR implementation in Pharmaceutical and Biopharmaceutical Industry: Technical and Regulatory Considerations
- 203: New GMP Regulations and Inspection Programs in Asia Pacific
- 303: Regulatory and Industry Perspectives of QbD
- 403: Process Validation: A Lifecycle Approach with Biotech Applications (Q11)
- 503: Biopharmaceutical Quality: Implementing PQS Elements (Q10)
Technology – Choose from a variety of subjects including nanotechnology, sterile products and strategies.
- 106: Nanotechnology in the Pharmaceutical Industry
- 206: Innovation in Laboratory and Production Operations
- 306: Strategies for Raw Material Variability
- 406: Sterile Products Processing Update
- 506: A Strategic Approach to Containment Systems: An Integrated Process from Concept to Use
- 509: Advanced Aseptic Processing Utilizing RABS and Isolators
