About
Experience in quality and compliance in medical device software development
As a compliance and quality lead at HTEC, Miloš has outstanding experience in helping evangelize the importance of quality and compliance in medical device software development.
He joined HTEC to, as he explains, “help HealthTech ecosystems overcome hurdles ahead before starting to smooth the path for disruptive medical technologies and benefit patients globally.”
Industry
Healthcare & Life Sciences
Podcast
FastForward with Milos Cigoj
Listen on:
Recent Publications
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Greenlight Guru: Advancing a Quality Management Solution by Implementing a Modular Approach
Greenlight Guru, a leading cloud-based platform purpose-built for MedTech companies to bring life-changing products to people, approached HTEC to help them build an independent, more scalable, smarter, resilient and modern architecture that would allow the client to advance their Quality Management Software and speed their time-to-market.
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Risk Management in the Medical Device Lifecycle: Discovery and Prototyping
Executive Summary: Risk management is the backbone of your medical device product development lifecycle — a guideline allowing you to turn risk into a value-add type of activity. To help you understand the key role Risk Management has throughout the entire product lifecycle, we talked with a number of experts coming from Greenlight Guru and HTEC Group…
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AI in Medical Devices and Healthcare: Challenges and What Lies Ahead
Artificial intelligence (AI), machine learning (ML), and deep learning (DL) have enormous potential to alter the healthcare sector, bringing significant advancements in diagnostics, tailored treatment, and efficient patient care. To ensure the responsible and ethical development and application of these technologies, it is crucial to acknowledge the challenges and problems that go along with these…
