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It is our silver anniversary and we are excited to host our 25th annual ISPE-CaSA Technology Conference. The planning process is underway and we are seeking speakers to help solidify our education track. This year will feature the latest technology and forward thinking concepts that relate to our local industry and beyond.
The deadline for abstracts to be considered for ISPE-CaSA Technology Conference 2018 is Friday October 20th, 2017. Whether it involves an innovative use of technology, or a novel approach to life sciences, consider submitting an abstract for a podium presentation across one or more pf these educational tracks. All vendor companies are strongly encouraged to partner with an end user to present a case study or panel discussion during their presentations. We will have a Young Professional 101 Series track, so please take this into consideration as you are submitting your topics. You can submit more than one abstract per company and it can be the same topic for entry level (101 series) and intermediate – advanced for the education track.
The format features:
Deadline for submissions: Friday, October 20, 2017.
Submitters will be notified of selection: by mid-December 2017
The conference planning committee will base its selections on general interest in the topic.
If you have any questions, please reach out to Jennifer Lauria Clark at email@example.com.
| SUBMISSION GROUPS||SUBMISSION SUB GROUPS |
|Automation||Cloud-Based SCADA Systems, Control System Virtualization, Lean Automation Architecture, Minimizing Validation Impact, Pre-Validated Code Module Libraries, Process Automation Controllers, Thin Client HMI/SCADA Systems, Other|
|Biotech||Futureof Biologics, Single Use Technology, Advancing Aseptic Design, ProcessDevelopment, Small Scale, Technology Transfer, Other|
| Compliance Trends||Data Integrity, Sterilization, Design Review, Cleaning Validation|
| Devices and Equipment||Medical Devices, Medical Equipment, Laboratory Devices, Other |
New Design Technologies, Efficient Work Practices, Other, Benchmarking - How to Conduct FDA
|FDA||Quality Metrics, 483 Observations, Other, 483 Observations, Quality Metrics|
|Information Management Systems||Cloud Historians, Data Analytics, Enterprise & Automation System Integration, IIoT(Industrial Internet of Things), Network & Control System Security, Other|
| Investigational Products||Other|
|Maintenance and Reliability||Maintenance , Reliability, Shutdown Optimization, Other|
|Manufacturing Operations||NewProject , Existing Project , Facility of the Future - New technologies,Employee of the Future, FOYA Winner, Sterile, Lean/Six Sigma, Other,Project Management, Single Use Filling Systems, OptimizingBiomanufacturing Operations, Innovations in Filling|
|Quality||Quality Culture, Quality Metrics, Other|
|Safety||Safety, Lessons Learned|
|Serialization||Compliance, Driving Business Value, Trends & Development, Other|
|Standards||New Standards, New/Existing Baselines|
| Supply Chain||Vendor Audits, Cold Supply Chain, International, Other|
| Women in Pharma||Engineering, Quality, Entrepreneurs, Other|