3rd Annual Lyophilized Product and Process Development - July 27-29, 2005 - Bethesda, MD

3rd Annual Lyophilized Product and Process Development
July 27-29, 2005 - Bethesda, MD
Bethesda Marriott
To successfully optimize lyophilized product and process development, it is imperative to fully comprehend the fundamental principles and approaches as well as be familiar with the most recent technological developments. The Institute for International Research is pleased to bring you the Second Annual Lyophilized Product and Process Development seminar which addresses the key issues for optimizing lyophilization products and cycles in a practical, easy to follow format.
Building on the success of our launch event last year and our Lyophilization Technology seminars, Lyophilized Product and Process Development brings you interactive sessions with leading experts. The objective being to provide you with a working knowledge of how to optimize lyophilized products and cycles of new and existing products from the bench to a commercial scale.
Key issues addressed and learning objectives include:
Developing lyophilization cycles on existing and new products
Understanding the scientific principles and key parameters of freeze drying
Examining product and process design for robustness and ease of scale-up
Exploring the impact of formulation on lyophilization product development
Examining primary drying case studies: optimizing and manipulating independent variables
Determining best practices approaches for secondary drying
Exploring packaging considerations for lyophilized products
Assessing the pros and cons of current delivery devices
Exploring approaches to optimize scale-up of your freeze drying manufacturing operations
Analyzing the impact of containers and closures
Determining the compliance requirements from development through commercial manufacturing
Who should attend

Key issues addressed and learning objectives include:
Pharmaceutical, biotech and medical device companies, and any organization involved with freeze drying operations for drug and device companies should attend this event.
Professionals in the following fields would find this seminar to be of particular value:
Formulation
Clinical Manufacturing
Regulatory
QA/QC
Validation
Research and Development
Process Engineering
Specifically, professionals in the following roles would find this event to be of significant value
Process/Senior Engineer
Formulation Development Scientist (Formulator)/ Formulation Specialist
Project/Validation Engineer
Validation/Senior Scientist
Clinical Manufacturing Manager/Supervisor/Professional
QA Compliance Auditor/QA Manager
Production Manager/Supervisor/Chemist
Chemical Engineer
Process/Production Supervisor
Research Scientist/Technician
Sterile Filling Supervisor
Product Release Specialist
Research Associate
Manufacturing Technical Trainer
Freeze Drying Specialist
Who should attend

Key issues addressed and learning objectives include:
Pharmaceutical, biotech and medical device companies, and any organization involved with freeze drying operations for drug and device companies should attend this event.
Professionals in the following fields would find this seminar to be of particular value:
Formulation
Clinical Manufacturing
Regulatory
QA/QC
Validation
Research and Development
Process Engineering
Specifically, professionals in the following roles would find this event to be of significant value
Process/Senior Engineer
Formulation Development Scientist (Formulator)/ Formulation Specialist
Project/Validation Engineer
Validation/Senior Scientist
Clinical Manufacturing Manager/Supervisor/Professional
QA Compliance Auditor/QA Manager
Production Manager/Supervisor/Chemist
Chemical Engineer
Process/Production Supervisor
Research Scientist/Technician
Sterile Filling Supervisor
Product Release Specialist
Research Associate
Manufacturing Technical Trainer
Freeze Drying Specialist