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Dear friends and colleagues, This year's conference gives an update on all aspects of the application of parenteral products covering a broad range of topics. PDA is seeking scientific abstracts for presentations 30 minutes in length or abstracts for posters. The theme of this year's conference: Device Usability and Compliance. Suggested Topics include but are not limited to:
Factors influencing Selection of Injection Devices
End user needs: doctors, hospitals and patients
Human Factors, Patient Compliance, Safety Aspects
Market trends, patient compliance studies
Autoinjectors, pen systems, safety devices and add-ons
Patient selfmanagement
Electronic enabled delivery systems
Health economics
Advances in Pre-filled Syringe/Injection Device Technologies
Novel delivery systems
Materials, components, methods
Safety Devices
Supplier issues: Quality agreements, logistics, partnerships, cooperations
Combination products
Development and Manufacturing
Development, incl. PAT, QbD, Upscaling, Tech Transfer
Manufacturing technologies: Equipment, machines, IPC tools
Zero defect challenges
Aseptic processing, sterilization methods, single use systems
Packaging, labeling, track and trace issues
Contract manufacturing
New trends
Regulatory Trends and Inspection Issues
New guidances
Track and Trace
Container quality/functionality aspects
ICH guidances: impact on submissions and inspections
Abstracts for presentations must be received before May 15 and Poster abstracts by October 1.
Dear friends and colleagues, This year's conference gives an update on all aspects of the application of parenteral products covering a broad range of topics. PDA is seeking scientific abstracts for presentations 30 minutes in length or abstracts for posters. The theme of this year's conference: Device Usability and Compliance. Suggested Topics include but are not limited to:
Factors influencing Selection of Injection Devices
End user needs: doctors, hospitals and patients
Human Factors, Patient Compliance, Safety Aspects
Market trends, patient compliance studies
Autoinjectors, pen systems, safety devices and add-ons
Patient selfmanagement
Electronic enabled delivery systems
Health economics
Advances in Pre-filled Syringe/Injection Device Technologies
Novel delivery systems
Materials, components, methods
Safety Devices
Supplier issues: Quality agreements, logistics, partnerships, cooperations
Combination products
Development and Manufacturing
Development, incl. PAT, QbD, Upscaling, Tech Transfer
Manufacturing technologies: Equipment, machines, IPC tools
Zero defect challenges
Aseptic processing, sterilization methods, single use systems
Packaging, labeling, track and trace issues
Contract manufacturing
New trends
Regulatory Trends and Inspection Issues
New guidances
Track and Trace
Container quality/functionality aspects
ICH guidances: impact on submissions and inspections
Abstracts for presentations must be received before May 15 and Poster abstracts by October 1.
![Alison Bryant, senior consultant at Antea Group and communications director for the Healthcare Plastics Recycling Council (HPRC), addressed the crowd at the[PACK]out.](https://img.healthcarepackaging.com/files/base/pmmi/all/image/2024/05/Alison_Bryant.6644005a513b0.png?auto=format%2Ccompress&fit=crop&h=167&q=70&w=250)
