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On Demand Webcast
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Utah Chapter Webcast: Legal aspects of FDA regulatory Compliance: Preparing for an FDA Facility Inspection and Responding to a 483 Letter

Learn elements to a successful inspection strategy for adequate preparation and implementing an inspection plan before FDA knocks on your door.
inspection Member Knowledge Center 483 fda
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Chicago Chapter Webcast: IVDR Notified Body Update

Enjoy a two-hour engagement with a Notified Body on IVDR State of Implementation.
Notified Body IVDR Member Knowledge Center
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New York/New Jersey Chapter Webcast: Raising the Regulatory Voice

Hear from an expert with more than 35 years of experience in helping regulatory professionals communicate clearly, concisely, and persuasively.
negotiation Member Knowledge Center communication presentation skills
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Wisconsin Chapter Webcast: Embracing the Growth – An Update on MedTech in Asia

Learn about the region’s growth, hear about its regulatory issues, get business development insights, and hear about how the medical device market can advance through innovation and strategic effectiveness in Asia’s markets.
china asia Member Knowledge Center medtech medical device japan
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New York/New Jersey Chapter Webcast: OTCMonograph Reform Amongst the COVID Economic Recovery Package

With the passage of the CARES Act on 27 March 2020, the system regulating the majority of drugs on the U.S. market underwent significant reform. Learn about key elements of the new law and how current and future OTC products may be affected.
OTC Monograph Member Knowledge Center
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Colorado Chapter Webcast: Preparing for Compliance with EU MDR 2017/745 and Article 117

Learn strategies that can help your medical device company navigate the higher level of scrutiny and helpful advice on EU MDR technical documentation preparation.
EU MDR 2017/745 Member Knowledge Center Article 117
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Twin Cities Webcast: ISO 14971:2019 - Update Your Process to Meet the New Risk Requirements

Join this interactive presentation outlining the changes to ISO 14971. Hear from an industry expert with more than 30 years of experience.
Member Knowledge Center ISO 14971 Medical Devices
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New York/New Jersey Chapter Webcast: Aligning Regulatory and Access Expectations: Driving Towards Optimum Outcomes for the Key Stakeholders

Learn about addressing the expectations of regulators and HTAb’s from the earliest points of product development through the regulatory and HTA assessment processes in order to contribute to successful outcomes.
quantitative regulatory Member Knowledge Center qualitative health technology assessment bodies
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Boston Chapter Webcast: Navigating China’s Medical Device Regulatory Landscape Under NMPA Regulations

Eat your lunch and join the RAPS Boston Chapter online to dive more deeply into the challenges that regulatory professionals face when working on submissions to China’s National Medical Products Administration (NMPA).
china Member Knowledge Center medical device National Medical Products Administration
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RAPS Indiana Chapter: Lunch and Learn Webcast: How Not to Annoy Your Reviewer

Eat your lunch and join the RAPS Indiana Chapter online for tips and tricks on how to build a positive relationship with Food and Drug Administration (FDA) scientists.
Food and Drug Administration Best practices Member Knowledge Center Reviewers