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Products

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E-Book
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RF Article Series: Regulatory Intelligence and Policy

This collection provides everything you need to know about regulatory intelligence and policy.
business and leadership
E-Book
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RF Article Series: Regulatory Management and Leadership Strategies

This collection provides everything you need to know about regulatory management and leadership strategies.
business and leadership
E-Book
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RF Article Series: Risk Management Principles: A Global Perspective

Inside you will find a collection of insightful articles covering the latest risk management principles.
Quality Compliance and Risk
E-Book
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RF Article Series: Global Reimbursement Strategies

This is a one of a kind RAPS product; written and reviewed by volunteer subject matter experts in the regulatory profession. It’s a holistic approach to reimbursement in one convenient format.
regulatory strategy medical device
E-Book
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RF Article Series: Transitioning to the New EU MDR and EU IVDR

In the second Regulatory Focus (RF) article series, leading global regulatory experts share their valuable insights and practical experience on how to comply with the new EU MDR and EU IVDR.
eu medical device
E-Book
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RF Article Series: Orphan Drug Regulations: A Global Perspective

This is a one of a kind RAPS product; written and reviewed by volunteer subject matter experts in the regulatory profession.
pharmaceuticals
E-Book
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RF Article Series: Global Advertising, Promotion and Labeling Regulations: What you Need to Know

Inside you will find a collection of insightful articles covering global Advertising, Promotion and Labeling (APL) regulations.
APL
Webcast
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Advancing and Enabling Regulatory Science to Impact Policy at CDRH: The AIMBE FDA Scholars Program (On-demand Webcast)

The American Institute for Medical and Biological Engineering (AIMBE) Scholars will share what was required to gain this prestigious role and how relationships with the FDA staff have affected their futures in the medical device industry positively.
biologics and biotechnology
Online Course
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New EU Medical Device and IVD Regulations

RAPS Executive Director, Paul Brooks explains some of the changes in the new EU MDR/ IVDR.
eu medical device
E-Book
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RAPS 2018 Compensation and Scope of Practice Report

The compensation data provide individual regulatory professionals, employers, recruiters and other stakeholders insight into the market value of regulatory work and expertise, and allow comparison of differences in compensation based on variables such as job level, experience and education.
business and leadership