- What: This is a webinar showcasing how our partnership with Acumed benefited from the usage of our CAPTIS solution. We will be discussing how medical device organizations can achieve efficiency, save time and improve accuracy by incorporating automation into their systematic literature review and Post-Market Surveillance (PMS) document creation processes.
- When: June 29th, 2023, 10.00 – 11:00 ET
- Where: Online Event
- How: Register Here
- Why: Learn how to work efficiently alongside an external partner for MDR/IVDR compliance and explore the benefits of integrating exclusive technology designed to automate your literature and PMS documentation workflows.
This featured presentation will be led by a Celegence customer – Kim Carlson Banning, PhD from Acumed, and will be moderated by Celegence’s Manager for Medical Device Services, Smridula Hariharan. Our panelists will also be available for a live Q&A session after the presentation.
Across the medical device and diagnostics industry, there are common obstacles when producing compliant Clinical Evaluation Reports (CERs), Performance Evaluation Reports (PERs) and other PMS related documentation in an efficient manner.
With the overall expansion of requirements for EU market access, PMS documentation now takes far longer and requires more medical writers and reviewers to work on the same materials (articles, source documents, adverse event data, etc.) simultaneously.
Systematic literature searches were especially difficult using previous research practices, with consistent citations becoming especially inefficient and time-consuming. Manual workflows take hundreds of hours a month and slow down the creation and maintenance of documentation, which can place massive burdens on a medical writing team.
Leveraging technology solutions and PMS documentation process automation will save medical writing teams hundreds of hours of manual effort as well as significantly reduce the propensity for human error, improving the quality of your outputs.
You’ll learn how CAPTIS™ – our exclusive technology for EU MDR/IVDR compliance, helps to produce high-quality, sustainable, cost-effective, error-free and audit-ready systematic literature reviews for the device and diagnostic industry.