Celegence
Celegence, co-founded by Sonia Veluchamy and Punya Abbhi provides services and solutions to support the Life Sciences industry with regulatory affairs operations and strategy.
To learn more about our CEO, Sonia Veluchamy - https://www.celegence.com/sonia-veluchamy-ceo-chicago-bio/
As regulatory specialists, we work across all phases of the product lifecycle from regulatory strategy, authoring, and all aspects of established product maintenance, including submission management, publishing and health authority interaction. We leverage a global team of consultants to provide local regulatory insight, strategy and intelligence.
Our mission is to collaborate with our customers to deliver Regulatory Affairs efficiency that allows them to focus on what matters most: providing exceptional patient value. We support companies in ensuring regulatory compliance across the globe by providing fully trained resources who understand the regulations.
IDMP Webinar Series - Part 1: Data Management
IDMP Webinar Series - Part 2: Process Optimization
IDMP Webinar Series - Part 3: Cross Department Benefits
Celegence Webinar - Productivity Improvements for Cost-Effective CER Writing and Maintenance
Leveraging Technology to Optimize MDR Compliance Outsourcing and Partnership - Webinar
Optimizing CER and PMS Document Writing with Technology and AI – Webinar with Medtech Intelligence
Navigating Clinical Evaluation Excellence: A Strategic Guide for Medical Devices - Celegence Webinar
Demo - How CAPTIS™ Platform Helps Medical Writers
EU Pharmaceutical Reform: Unveiling Draft Legislation Impacts - Celegence Webinar
Strategies for Successful PMCF under EU MDR: Unlocking the Mystery – Webinar
Practical Advice and Next Steps to Ensure PLM Portal Readiness - Webinar
Mastering Compliance: Essential Insights into PMS Documentation - Webinar
Navigating the MDR/IVDR Conformity Assessment Maze: Pitfalls and Pathways - Celegence Webinar
Dossplorer New Functionality Sessions - June 2024 - Celegence
Discussing Regulatory Affairs: Leadership Perspectives & 2024 Survey Insights - Webinar
The New FDA LDT Regulations: Key Changes & Compliance Guide
Managing Global Regulatory Strategy & Compliance: Assessing Status, Gaps, and Needs - Webinar
New FDA LDT Regulations: Key Changes & Compliance Guide
The Art of Benefit-Risk Calculation – Essential Tools for EU MDR Mastery: Webinar
Efficiency in Regulatory Submissions: Apply the Power of Lean Authoring - Webinar
AI and Automation for Regulatory Compliance in Medical Devices – Smarter Data Management Webinar
How Does CAPTIS® Help Medical Writers Save Up to 60% of Time on Literature Search Reviews?
Webinar - Overcoming Regulatory Challenges for Cell & Gene Therapy Products: ATMP Success Insights
The Regulatory Landscape in 2025: What you need to know - Webinar
Beyond the Spreadsheet: The Silent Cost of Data Chaos in Regulatory Affairs - Webinar