Celegence CEO Sonia Veluchamy Featured in European Pharmaceutical Manufacturer
Our CEO Sonia A. Veluchamy shares valuable perspectives on lessening the regulatory burden for medical device suppliers and the pharma best practice around structured data re-use. Sonia outlines practical strategies around streamlining data, improved efficiency and gains for the industry
Article Highlights
- How a shift in approach towards smart documents can keep companies ahead of the curve
- Top challenges Medical Device companies are facing around bandwidth based on new research
- Opportunity to infuse technology such as GenAI coupled with industry-specific expertise
Read the full article in European Pharmaceutical Manufacturer
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.
