Pharma’s Data Secret That Medical Device Companies Should Adopt

In a recent article published on MedDevice Online, Celegence CEO Sonia A. Veluchamy shares her insights on Pharma’s data secret that medical device companies should adopt. The article discusses that the best practices being established in pharma is a distancing from the traditional document-centric approach and prioritizing smarter content creation.

• Best practices from pharmaceutical companies reducing the number of documents created by breaking down silos to share data and structure more efficiently
• New research conducted by Celegence and industry partners reveals 77% of regulatory departments in medical device teams are under-resourced
• Technology-enabled expertise, such as leveraging Artificial Intelligence (AI), specifically GenAI can help easy workflows with the right set up

Read the full article now on Med Device Online.

Sonia Veluchamy is the CEO at Celegence, where she spearheads technological innovations such as CAPTIS and Dossplorer to enhance regulatory compliance and efficiency. Sonia envisioned an opportunity to support life sciences companies in bridging the gap between regulatory intelligence and the operational activities associated with compliance.

Celegence has proven experience with medical writing for regulatory submissions. Our deep regulatory expertise, combined with advanced AI-Enabled technology solutions, positions us uniquely to handle the complexities of medical writing. We ensure that every document is not only compliant but crafted to expedite approval processes and facilitate market access. For more information about our services can benefit your regulatory processes, contact us today.