Overview

Pre-filled syringes and injection devices continue to be a growing market improving administration, compliance, safety, costs, and accuracy of drug delivery. New advances in materials of construction, manufacturing processes, injection processes and safety devices, and other technology improvements create a dynamic environment in the pre-filled syringe and injection device arena. Regulatory requirements, industry experience and evolving market trends are critical considerations to ensure a complete understanding of the application of pre-filled syringes and injection devices to drug delivery. The challenges of new product introduction and support of existing products require that companies be aware of new developments.

The 2008 PDA Universe of Pre-filled Syringes and Injection Devices brings together industry experts to share their experiences, new developments, regulatory considerations, challenges and industry trends in this exciting area. The topics discussed at this fifth annual PDA meeting on pre-filled syringes and injection devices will benefit those looking for a basic understanding of pre-filled syringes and injection devices as well as those looking for a more in depth presentation of current challenges and developments. This is a must attend event for all industry professionals involved in pre-filled syringes and injection devices.

Plenary sessions will cover topics such as:

• The supplier qualification and issues
• Materials of construction and considerations
• Filling and manufacturing concerns
• Regulatory and compliance aspects
• Case studies
• Injectors and alternative devices
• Safety systems and devices

Take Home Benefits

At the completion of this conference, attendees will be able to:

• Identify the benefits of pre-filled syringes and injection devices
• Identify safety systems
• Recognize major considerations during manufacturing and processing of pre-filled syringes and injection devices
• Describe regulatory and compliance concerns
• Utilize lessons learned from case studies in their respective companies
• Determine industry trends and new directions for pre-filled syringes and injection devices

Who Should Attend

Department
Operations | Regulatory Affairs | Manufacturing | Transportation | Packaging | Quality Assurance/Control

Job Function
Manufacture of Parenteral Products | Packaging Engineers | Stability Coordinators | Supply Chain | Logistics | Clinical Development

Contact

Jason Brown
Programs Manager
Tel: +1 (301) 656-5900 ext. 131
Fax: +1 (301) 986-0296
Email: brown@pda.org