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Welcome to the RAPS Member Knowledge CenterLog in to access to all the great educational resources you get with your RAPS membership. 

Products

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E-Book
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e-Book: Choosing the Right Regulatory Career

Learn about the regulatory role in small and large companies and the differences for regulatory professionals working for device and pharmaceutical firms.
biologics and biotechnology career development pharmaceuticals medical device
Webcast
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Webcast: Designing Your Career as a Regulatory Professional

You know professional development is important, but it's not that easy to come up with plans that make a difference in performance.
On Demand Webcast
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On-demand Webcast: We Need to Talk

This webcast explores internal communication know-how and persuasion strategies to improve cooperation and effectiveness at work.
business skills business and leadership
Online Course
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Acronyms & Definitions

This page is a valuable reference tool for those new to regulatory as well as experienced professionals. It is also a handy guide for those preparing for any of the RAC exams.
Member Knowledge Center
On Demand Webcast
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On-demand Webcast: 21 CFR 820 Quality System Regulation and ISO 13485 Medical Devices

The RAPS Philadelphia Chapter webcast covering 21 CFR 820 quality system regulation and ISO 13485 medical devices.
medical devices quality
On Demand Webcast
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On-demand Webcast: China's Clinical Requirements Under the New Registration System

This webcast will introduce the requirements and the process on record filing of clinical trials of medical devices and its related government authorities.
medical devices submission and registration clinical regulatory strategy preclinical
On Demand Webcast
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On-demand Webcast: China Regulations on Medical Devices - Adverse Event Monitoring and Re-evaluation

Under the new regulation, CFDA will perform a more strict post-market surveillance than before. This webcast will provide you with new regulatory requirements and help you establish internal procedures.
medical devices submission and registration postmarket surveillance
On Demand Webcast
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On-demand Webcast: CFDA Registration Requirement for Imported Class II/III Medical Devices

This webcast will help foreign establishment get prepared through the learning of the overall China regulation framework for imported medical devices and provide a detailed introduction of CFDA registration process, requirement and potential cost.
medical devices submission and registration
On Demand Webcast
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On-demand Webcast: The Supervision of Medical Device Label and Instruction for Use in China

On-demand Webcast: The Supervision of Medical Device Labeling and Inspection
medical devices labeling
On Demand Webcast
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On-demand Webcast: Overview of China's Regulatory System & New Medical Device Regulations

An on-demand recording of the RAPS Webcast, Overview of China Regulatory System and New Medical Device Regulations.
medical devices submission and registration postmarket surveillance regulatory strategy