Celegence CEO Sonia Veluchamy Featured in International Pharmaceutical Industry
Our CEO Sonia A. Veluchamy shares valuable perspectives in the Volume 16 Issue 3 of International Pharmaceutical Industry on what the medical device sector can learn from pharma’s structured data challenges.
Article Highlights
- Technology investment areas planned in Medical Devices around MDR compliance and maintenance, Regulatory Intelligence and dedicated systems will help digitalize operations
- Structured data management with approaches such as Lean Authoring reduce documentation and simplify submissions helping organizations and Health Authorities
- Expertise plus targeted use of Artificial Intelligence (AI), specifically GenAI can help teams especially with the right industry partner
Read the full article in International Pharmaceutical Industry
Celegence’s Expertise
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.
