Manicka Sundaram

Manicka Sundaram

26 Jun, 2025

Manicka Sundaram R is a seasoned regulatory and compliance professional with over 14 years of experience, including a decade in the medical device industry. He specializes in design history file remediation, risk management, and compliance with global regulatory standards.

Other Related Articles

EUDAMED Becomes Fully Mandatory from 28 May 2026: What Medical Device & IVD Manufacturers Need to Know

Blog Medical Devices

EUDAMED Becomes Fully Mandatory from 28 May 2026: What Medical Device & IVD Manufacturers Need to Know

08 Dec, 2025

CMC Technical Writing: A Critical Enabler During Product Development

Blog Pharmaceutical

CMC Technical Writing: A Critical Enabler During Product Development

02 Dec, 2025

AI in Medical and Technical Writing: Moving Beyond the Hype to Real-World Impact

Blog Medical Devices

AI in Medical and Technical Writing: Moving Beyond the Hype to Real-World Impact

20 Nov, 2025

What is a Service+Tech Model? – The Fastest Path to Integrating AI into Regulatory Operations

Blog Medical Devices

What is a Service+Tech Model? – The Fastest Path to Integrating AI into Regulatory Operations

11 Nov, 2025

From Spreadsheets to Strategic Assets: Key Takeaways from Our Regulatory Data Management Webinar

Blog Pharmaceutical

From Spreadsheets to Strategic Assets: Key Takeaways from Our Regulatory Data Management Webinar

04 Nov, 2025

Sonia Veluchamy Named Among Crain’s Top Health Tech Leaders 2025

Company News

Sonia Veluchamy Named Among Crain’s Top Health Tech Leaders 2025

28 Oct, 2025

Regulatory Approvals in Africa: Key Frameworks, Challenges, and Emerging Trends

Blog Pharmaceutical

Regulatory Approvals in Africa: Key Frameworks, Challenges, and Emerging Trends

21 Oct, 2025

AI and Data Privacy & Compliance: How is Your Data Protected?

Blog Medical Devices

AI and Data Privacy & Compliance: How is Your Data Protected?

14 Oct, 2025

View All