Pinnacle Programme
2011 Global Sponsor
Platinum Sponsor
Gold Sponsor
Bronze Sponsor
Education Sessions by Track
Facilities and Project Delivery
Tight budget? Tight schedule?
Learn how you can integrate the demands of GMP requirements despite business constraints and project realities. Review case studies and engage in workshop forums to improve your ability to deliver your next project on time, on budget, and in compliance. Capital project managers, facility designers, owners, and contractors involved in project delivery will benefit from these programs.
Hear from companies and governmental agencies including:
Amgen • MedImmune • Roche • Cephalon • Eli Lilly & Co. • Becton Dickinson and Co. • Merck & Co., Inc. • Oso Biopharmaceuticals • US Environmental Protection Agency
- 104: The New Workplace: New Trends in the Design of the Office and Laboratory Workspace for the Pharmaceutical and Biotechnology Industry
- 108: Planning for Expansion
- 204: Making Sustainability Pay: Lessons Learned and Best Practices
- 208: Identifying the Best Resources to Fit Your Projects’ Needs
- 304: 2011 Facility of the Year Awards Category Winners Presentation
- 306: Pharmaceuticals in the Environment: A Regulatory Perspective
- 308: Establishing Best Methods of Communication for Your Projects
- 404: 2011 Facility of the Year Awards Category Winners Presentation (continuation)
- 408: Keeping Your Project Team Going in the Right Direction
- 505: OSD - Don’t Let the Process Control You!
- 506: Green OSD Pharmaceutical Production
- 508: The Project Manager’s Role in Dispute Resolution
Investigational Products
The world of clinical supplies will be entering one of its most dynamic regulatory phases ever.
Learn what’s on the horizon in the areas of Interactive Response Technology (IRT) and Supply Chain Optimization, and discover novel approaches to current industry challenges. Preview Good Practice Guides on the topics of IRT, Comparators and Booklet Labels currently in development.
Hear from companies and governmental agencies including:
GlaxsoSmithKline • Genzyme • Pfizer • Merck & Co., Inc. • AstraZeneca • Medicines and Healthcare Products Regulatory Agency (MHRA) UK
Manufacturing Operations, Including Emerging Markets
Supply chain quality assurance… supply chain reliability…operational excellence…China…India…ASEAN… South America…Eastern Europe.
Executing successful business operations in an increasingly cost-constrained and globally diverse manufacturing environment is challenging. Regulators and industry professionals present state-of-the-art approaches and business-savvy techniques to help you meet those challenges. Professionals involved in site selection and permitting, manufacturing operations, supply chain management, and related fields will find these sessions beneficial.
Hear from companies and governmental agencies including:
Johnson & Johnson • AstraZeneca • Pfizer • Eli Lilly & Co. • GlaxoSmithKline • Celgene Corp. • Shanghai FDA • US Department of Homeland Security • California State Board of Pharmacy
- 102: How to Succeed with Facility Capital Investments in China
- 202: Secrets to Successful Manufacturing Facility Projects in BRIC Countries
- 206: Supply Chain Integrity and Brand Protection for Healthcare Products
- 207: Operational Excellence - A Foundation for Quality
- 302: Delivering Manufacturing Facilities in Asia: Market Understanding and Risk Management
- 402: GMP and CMC Regulations in Asia: Modernizing Initiatives and Current Regulatory Environment in China, India and ASEAN Markets
- 406: Supply Chain Integration to Maximize Profits and Compliance
- 502: Pharmaceutical Manufacturing in Central and Eastern Europe
Regulatory
ISPE is the premier organization for practical applications in a regulated GMP environment.
Help your organization adopt innovative approaches to regulatory compliance: reduce cost, reduce time and effort, manage quality risks, and improve quality of marketed products. Put your regulatory and GMP questions to a forum of distinguished panelists. Hear case studies and learn about new Guidance Documents.
Commissioning and validation professionals, those involved in quality assurance and regulatory compliance functions, and product and process development personnel will acquire critical information to help their daily professional work.
Hear from companies and governmental agencies including:
Abbott • Bayer • Eli Lilly & Co. • FDA Investigators • Johnson & Johnson • Roche
- 105: Critical Utilities
- 203: Introduction and Overview of the New ISPE Quality Risk Management Guidance Documents for C&Q
- 205: Regulatory Affairs Forum
- 303: Pharma Manufacturer’s C&Q Risk Approach Task Team Forum III - Process and Practices
- 305: Launching the QbD Series and Implementing ICH Q10: Moving Pharma Quality Systems Program Forward
- 307: Automated System Testing: Driving Process Performance and Data Integrity Part 1
- 403: Beyond ICQ: An ASTM E2500, Verification Leveraging, Project Profile
- 405: PQLI®/PAT - Moving Beyond ICH Q8, 9, and 10 Concepts: Biotech QbD Realization Case Studies Leveraging PAT
- 407: Automated System Testing: Driving Process Performance and Data Integrity Part 2
- 503: Early Stage Planning and Overall Project Controls for Large C&Q Projects
- 504: Combining Commissioning and Qualification: A Non-conventional Streamlined Validation Approach
- 507: Product Supply and Network Challenges in Latin America
Technology
The key to both compliance and business success is technology that delivers reliable, efficient, quality products without contamination.
From the API process to final aseptic filling or solid dosage packaging, hear about the latest in manufacturing equipment and process technologies.
Engineers, scientists, service consultants, and operations personnel will benefit from these sessions.
Hear from companies and governmental agencies including:
Cook Pharmica • Genentech • Pfizer • US Department of Health and Human Services • Eli Lilly & Co. • Hospira
- 101: Advanced Aseptic Processing Utilizing RABS and Isolators
- 201: Aseptic Processing: The Future of Technology, Regulations, and Manufacturing Operations
- 301: Current Trends in Disposable Applications
- 401: Advancements in API Process Technology
- 501: Disposables - Early Phase / Clinical Manufacturing Approach Utilization Disposable Applications
