4 past events found
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New FDA FSMA Rules on the Sanitary Tran...
Transportation and Logistics food transportation food safety rules are currently being finalized by the U.S. Food and Drug Administration (FDA). Under congressional instructions, the Food Safety Modernization Act (FSMA) requires the FDA to establish rules to improve, audit and enforce new food transportation rules. The rules provide a significant focus on foods not completely enclosed by a container, risk reducing adulteration prevention, pers...
March 16-17, 2017
Organizer: GlobalCompliancePanel
Location: Tukwila, WA
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Quality by Design using Design of Exper...
This seminar focuses on how to establish a systematic approach to pharmaceutical development that is defined by Quality-by-Design (QbD) principles using design of experiments (DOE). In addition, this course teaches the application of statistics for setting specifications, assessing measurement systems (assays), developing a control plan as part of a risk management strategy, and ensuring process control/capability. All concepts are taught with...
February 2-3, 2017
Organizer: GlobalCompliancePanel
Location: Tukwila, WA
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Seminar on Risk Management in R&D, QA/Q...
Course "Applied Statistics, with Emphasis on Risk Management in R&D, QA/QC, and Manufacturing" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: The 2-day seminar explains how to apply statistics to manage risk in R&D, QA/QC, and Manufacturing, with examples derived mainly from the medical device design/manufacturing industry. The flow of topics ov...
September 22-23, 2016
Organizer: GlobalCompliancePanel
Location: Tukwila, WA
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Conference on Latest FDA Proposed Chang...
Course "Bullet Proof 510(k) and Latest FDA Proposed Changes to the Process" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: This Two-day course is a primer and overview to the premarket notification process, i.e., a 510(k). A 510(k) is a premarket submission made to FDA to demonstrate that your device to be marketed is at least as safe and effective, tha...
September 22-23, 2016
Organizer: GlobalCompliancePanel
Location: Tukwila, WA
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