WEBINARS

Our most recent webinars.

[FREE WEBINAR] It’s All Interconnected: Hidden Traps That Can Derail Your PER: Lessons Learned from the MDR-Compliant CER Writing Experience

[FREE WEBINAR] IVDR Readiness: Creating a Blueprint to Build a Strong PER

[FREE WEBINAR] Integration of Plain Language Content and Infographics into HCP Communication Channels: Strategies to Enhance HCP Engagement

[FREE WEBINAR] Developing Effective Patient-Focused Content: Writing Plain Language Lay Summaries and SSCP Patient Sections

[FREE WEBINAR] Critical Concepts Webinar Medical Device Software: Approaches to Determining Risk Classification, Qualification, and Safety and Performance Outcomes

[FREE WEBINAR] Stay Focused: The Purpose of the SVR and Tips for Building a Strong PER Foundation

[FREE WEBINAR] Plain Language Communication in Healthcare Part 1 Webinar

[FREE WEBINAR] New Requirements for In Vitro Diagnostics: Lessons Learned from the AAMI/FDA/BSI Annual Conference

[FREE WEBINAR] Critical Concepts: A Deep Dive into MDR and IVDR Device Classification and Data Collection Strategies

[FREE WEBINAR] Critical Concepts: The Role of Post Market Activities in Establishing Data Sufficiency

[FREE WEBINAR] CER Critical Concepts: Effectively Telling the Story of the CER – Focus on S&P Objectives, Acceptance Criteria, Clinical Benefits and Risk-Benefit Analysis

[FREE WEBINAR] Demonstration of Sufficient Evidence and Regulatory Strategy Alignment in the Clinical Evaluation Process

[FREE WEBINAR] How to Establish the State of the Art Within the Scientific Validity Report

[FREE WEBINAR] How to Establish the State of the Art Within the Scientific Validity Report

[FREE WEBINAR] Are You Reg. Ready? Get your medical affairs team primed to manage new regulatory requirements.

[FREE WEBINAR] Driving Innovation to Success in the Market: Strategic Considerations

[FREE WEBINAR SERIES] How to Assess Your CER for MDR Readiness

[FREE WEBINAR] State of the Art: Building a Solid Foundation for your PER to Support IVDR Readiness

[FREE WEBINAR] Hidden Traps That Derail PER Preparedness: Lessons Learned from the MDR-Compliant CER Writing Experience

[FREE WEBINAR] Leveraging the MDR experience for IVDR: Tips for Successful Performance Evaluation and PMS/PMPF Processes

[FREE WEBINAR] Effective Corporate Scientific Communication: Strategies to Support your Corporate Narrative and Maximize the Real-World Impact of your Data

[FREE WEBINAR] Hidden Traps That Derail PER Preparedness: Lessons Learned from the MDR-Compliant CER Writing Experience

[FREE WEBINAR] Hidden Traps That Will Derail Your CER: Answer these critical questions before you start writing

[FREE WEBINAR] A Practical Guide: Conducting Systematic Literature Reviews in Support of IVDR Readiness

[FREE WEBINAR] How to Assess Your CER for MDR Readiness, Part 2: Clinical Data Sources, Equivalence, and Risk/Benefit Analysis

[FREE WEBINAR] Live Q&A Follow-Up: How to Assess Your CER for MDR Readiness, Part 1

[FREE WEBINAR] How to Assess Your CER for MDR Readiness, Part 1: State of the Art, Safety & Performance Criteria, Equivalence and Systematic Literature Review

[FREE WEBINAR] Systematic Literature Review to Help Meet MDR Requirements

[FREE WEBINAR] Systematic Literature Review: How to Empower Data-Driven Decision Making

[FREE WEBINAR] The Art of State of The Art: All You Need to Know

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Criterion Edge is a distinguished global provider in the MedTech industry, dedicated to advancing compliance and enhancing market success for Medical Device, Pharma, and IVD companies through expert regulatory, scientific, and clinical writing services.

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