PCI 3.06.26
Wallonia

Current Edition

Current Features

Biomanufacturing

Mastering ADC Bioconjugation: From DAR Control to Efficient Free Payload Removal

Continue reading

Upcoming Events

Bioprocessing summit
DDL 2026
ELRIG Drug Discovery USA
Biotechnology Show 13.02.26
PFS & Injectable drug devices west coast

Advertisement

Advertisement

A&M Stabtest April 26

Advertisement

Biopharma Group – 19th March 2025

Advertisement

Micron View

Enhanced Compliance Inc. (ECI) Appoints Taranjit S. Samra as Head of Medical Device Software Engineering, Cybersecurity and AI

Strengthens ECI’s AI & Digital Transformation capabilities to help clients develop the next generation of software-enabled medical technologies

 Enhanced Compliance Inc. (ECI), a global life sciences partner delivering integrated quality, regulatory, and compliance expertise, combined with hands-on engineering execution and advanced packaging and laboratory testing, today announced the appointment of Taranjit S. Samra, DRSc, MSEE, RAC, as Head of Medical Device Software Engineering, Cybersecurity and AI, reporting to Shital Patel, Chief Operating Officer.

“Software, cybersecurity and AI are fundamentally reshaping the future of medical technology,” said Brijesh Patel, Chief Executive Officer of ECI. “Taranjit brings the strong combination of technical depth, regulatory expertise and strategic leadership needed to help our clients navigate this evolution with confidence. His appointment significantly strengthens ECI’s ability to support organisations developing the next generation of connected, software-enabled and AI-powered medical technologies.
Taranjit brings nearly 30 years of experience spanning medical devices, diagnostics, software, digital health, AI, precision medicine, biotechnology and clinical laboratories. Throughout his career, he has helped innovative healthcare technology companies build quality systems and regulatory frameworks that enable organisations to successfully commercialise emerging technologies while meeting increasingly complex global regulatory requirements.

His experience includes leading quality and regulatory transformations, implementing enterprise Quality Management Systems (QMS) aligned with FDA QMSR and ISO 13485, supporting FDA Class III PMA approvals, preparing organisations for first-time FDA inspections, and developing modern approaches to software quality, cybersecurity and AI governance. He has held leadership roles with organisations including Verily (Google Life Sciences), Illumina, Caris Life Sciences, Tempus AI, Guardant Health, Grail, Varian Medical Systems and Sanmina-SCI.

With deep expertise in medical device software and regulatory science, Taranjit has worked closely with the FDA’s Digital Health initiatives, authored publications on medical device software and global regulatory strategy, and taught graduate-level Regulatory Science. His work continues to help shape practical, risk-based approaches for AI-enabled quality systems, software engineering and regulatory compliance.

In his role at ECI, Taranjit will lead the company’s Medical Device Software Engineering, Cybersecurity and AI practice, partnering with life sciences organisations developing Software as a Medical Device (SaMD), Software in a Medical Device (SiMD),AI-enabled technologies, connected medical devices and digital health solutions. He will help clients navigate evolving global regulatory expectations while implementing modern software engineering, cybersecurity, quality and AI governance frameworks.

His appointment further strengthens ECI’s AI & Digital Transformation solution while enhancing the company’s ability to support clients developing software-enabled medical devices, connected products, cybersecurity programs and AI-driven technologies across the entire product lifecycle.

“I’m excited to join ECI at such an important time for the life sciences industry,” said Samra. “Artificial intelligence, software and connected technologies are transforming how medical products are developed, regulated and maintained throughout their lifecycle. ECI’s integrated consulting model uniquely positions us to help organisations successfully navigate this transformation while maintaining the highest standards of quality, compliance and patient safety. I look forward to partnering with our clients as they bring the next generation of healthcare innovation to market.”

Advertisement

Richter: Wed 23 October 2024, 09:03

Advertisement

Aseptic Tech

Advertisement

Steribar – 12.05.2025

Advertisement

PharmExcel

Advertisement

Polypure hompage

Advertisement

Gen Xpro

Advertisement

Alphinity