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On Demand Webcast
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Best Practices for Building An Efficient Literature Review Process (On-Demand Webcast)

This webinar provides valuable information to help manage the dramatically increased workload as a result of the new EU MDR.
medical devices packaging project management labeling writing Risk Management advertising and promotion compliance
On Demand Webcast
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China NMPA and US FDA Emergency Approval and Implications to Life Science Companies Relating to COVID-19 (On-Demand Webcast)

Learn about China NMPA's response to the COVID-19 pandemic.
medical devices drugs quality manufacturing compliance biologics IVD
On Demand Webcast
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PMS Requirements of the EU MDR: Implementation Challenges and Solutions (On-Demand Webcast)

We have a choice: Continue to apply Band-aids to our PMS processes and procedures, or think long-term and get it right for good. We're sharing several real examples that have worked and know what the notified bodies actually want to see.
medical devices postmarket surveillance regulatory strategy Risk Management postmarket compliance
On Demand Webcast
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Strategic Role of the RA Professional (On-Demand Webcast)

Learn how you can positively impact your cross functional team interactions and potentially bring new products to market faster. Presented by RA professionals who have experience in premarket through post market activities.
medical devices project management career development regulatory strategy Communications R&D
On Demand Webcast
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EU MDR Prep: Translation Requirements That Will Make or Break Your Devices In Europe (On-Demand Webcast)

Medical device regulatory experts will provide insights about how the current language requirements will change with the MDR. Experts will cover highlights of the major changes with the EU MDR, and the MDR’s specific requirements for translation.
project management labeling regulatory strategy writing Quality Assurance compliance
Webcast
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21 CFR 820 Quality System Regulation and ISO 13485 Medical Devices (On-demand Webcast)

The RAPS Philadelphia Chapter webcast covering 21 CFR 820 quality system regulation and ISO 13485 medical devices.
Quality Compliance and Risk medical device
Webcast
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Regulatory Intelligence and Its Value in Regulated Industry (On-demand)

The webcast will include the fundamentals of global regulatory intelligence, and how it can be used to influence regulatory decision making throughout a development program and lifecycle management of a therapeutic product.
regulatory intelligence
On Demand Webcast
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How to Facilitate Regulatory Meetings (On-demand Webcast)

This webcast will help prepare regulatory professionals for the difficult task of meeting facilitation. Learn to effectively facilitate teams as they prepare for, conduct, and debrief important meetings
government affairs Communications
On Demand Webcast
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What You Need to Know About FDA Regulation of Medical Product Promotional Labeling (On-demand Webcast)

This webcast will provide an overview of the book content and discuss considerations for implementing quality systems and procedures that will help you remain in compliance with promotional labeling regulations.
medical device advertising and promotion
Webcast
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How to Better Manage Quality and Risk with a Global Change Control Strategy (On-demand Webcast)

Learn about the contributing factors to building change control system that can help manage risk as well as metrics to consider to drive success.
Quality Compliance and Risk