Learn what the recently released CDSCO draft guidelines for medical device software within India actually mean.
Integrating Git version control with validation systems automates medical device software traceability, ensuring instant ...
Global Medical Transcription Software Market: Transforming Healthcare Documentation Through Innovation ...
Butterfly Network (NYSE:BFLY) announced today that it launched Compass AI, the latest generation of its enterprise software ...
Beyond Tariffs: The Software Supply Chain Risks Every Medical Device Manufacturer Should Be Watching
By reframing security as an investment rather than a cost, MDMs can reduce risk exposure, improve compliance readiness, and ...
MES software is transforming medical plastics manufacturing by automating compliance and enabling real-time traceability.
Matic Expands AI Suite and Joins Forces with UrgentIQ to Advance EHR Automation and Revenue Integrity Scribematic rebrands to Matic as company expands from clinical documentation to a full ...
BrainChip AKD1500 is an ultra-efficient Edge AI co-processor delivering up to 800 GOPS while consuming just 300 mW of power, ...
New Delhi: In a move to align India’s regulatory framework for medical device software with global standards, the Central Drugs Standard Control Organization (CDSCO) has released new draft guidelines ...
A DevOps-based framework integrates automation, continuous integration, and agile methodologies to enhance medical device software development.
Early adoption results have been significant. In a recent pilot, Pure Global’s Brazil team cut document assembly time for 27 ...
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