2020 - Beyond NanoEHS Risk Assessments - Leading at the Interface of Science and Business
Date2020-10-08 - 2020-10-09
Deadline2020-09-29
VenueOrlando, FL, USA - United States
KeywordsNanoEHS Risk Assessments; NanoEHS; Advanced materials research
Topics/Call fo Papers
Describe a tiered-approach framework for nanomaterial environmental health and safety (nanoEHS) risk assessments
Apply scientific principles and strategic thinking to a tiered-approach framework case study of a new technology
Apply context to the identification of potential hazards and exposures
Identify the benefits of Life Cycle Analysis thinking
Determine, when using a tiered-approach framework, additional experiments are valuable
Identify common and advanced material science instrumentation
Identify best practices for measuring nanomaterials
Identify current trends in advanced materials research
Describe how to validate low cost in-process production measurements to ensure product safety and quality
Communicate more effectively on cross-functional teams
Identify lessons learned from risk assessments for improving or developing a quality management system
Identify approaches for creating a culture for success through inspirational leadership
Identify the product development lifecycle, and when and how EHS should become engaged to maximize product launch success
Apply scientific principles and strategic thinking to a tiered-approach framework case study of a new technology
Apply context to the identification of potential hazards and exposures
Identify the benefits of Life Cycle Analysis thinking
Determine, when using a tiered-approach framework, additional experiments are valuable
Identify common and advanced material science instrumentation
Identify best practices for measuring nanomaterials
Identify current trends in advanced materials research
Describe how to validate low cost in-process production measurements to ensure product safety and quality
Communicate more effectively on cross-functional teams
Identify lessons learned from risk assessments for improving or developing a quality management system
Identify approaches for creating a culture for success through inspirational leadership
Identify the product development lifecycle, and when and how EHS should become engaged to maximize product launch success
Other CFPs
- FDA Recalls - Before You Start, and After You Finish
- Clinical Data Management (CDM)
- Validation, Verification and Transfer of Analytical Methods (Understanding and implementing guidelines from FDA/EMA, USP and ICH)
- Analytical Instrument Qualification and System Validation
- Lifecycle Management of Analytical Methods and Procedures - according to new FDA and USP guidelines
Last modified: 2020-05-19 22:49:34