BEIJING, [MICHAEL R. SISAK, AP News] — As healthcare digitalization advances worldwide, few technical experts have bridged industry standards, real-world clinical performance, and cross-border compliance as consistently as Qi Zhengyang, a recognized leader in medical and health technology.

In a rare exclusive interview with Reuters, Qi detailed how his original technical systems and evidence-based industry standards are solving persistent pain points: data security risks, compliance costs, inefficient cross-institutional data sharing, and talent gaps in medical IT.
Over recent years, Qi has led the development of five industry standards focused on medical cloud-native compliance, medical IoT access security, AI operational early warning, server elastic scaling, and automated compliance auditing.
These standards integrate widely recognized international frameworks (including HIPAA and CLIA) with on-the-ground clinical needs, defining 205 quantifiable technical indicators to create consistent, implementable guidelines.
Adopted across educational associations, universities, and medical enterprises, the standards have helped lower industry-wide compliance vulnerabilities and reduce redundant system redevelopment for institutions.
“Standards work only if they are practical and fair,” Qi said. “They should help large hospitals and smaller clinics alike, without requiring full infrastructure overhauls.”
Qi has developed 15 original copyrighted technical systems and three commercial-grade software platforms, all built to turn standards into stable, high-performance tools.

Key real-world results include:
1. MedSecShield: Reduces medical data breach risk from an industry average of 32% to 0.5%, while cutting compliance audit cycles from 15 days to 3 days.
2. MedServerPro: Improves server resource utilization and supports stable operation under peak load. At U.S. CLIA-certified laboratory Vibrant Wellness, it maintained uninterrupted service during high-traffic periods and lifted one-pass HIPAA audit performance.
3. MedDataSync: Lowers duplicate examination rates and shortens cross-institutional data integration timelines, supporting more efficient regional medical collaboration.
These systems have been deployed across more than 216 medical institutions and enterprises in China and North America, with verified operational improvements in safety, speed, and cost control.
As a member of the Expert Steering Committee for the National Applied Talents Training Program (Medical and Health Technology), Qi designed a structured training model that combines technical skill, compliance literacy, and clinical scenario practice.
He has published professional textbooks used by universities and built practical teaching centers that have raised graduate job adaptation rates from 55% to 85%. His outreach programs provide free technical support to universities and grassroots medical institutions, expanding access to capable, compliant digital systems.
Qi said his team is enhancing cross-regional compliance modules to support safer, regulated cross-border medical data flow, while continuing to refine AI-driven compliance auditing and predictive risk monitoring.
“The goal is steady, sustainable improvement,” he noted. “Medical technology must serve patients and institutions reliably — secure, compliant, and efficient.”
Qi’s work demonstrates how targeted, evidence-based innovation can elevate an entire industry without fanfare: measurable results, broad adoption, and sustained value for global healthcare.
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By MICHAEL R. SISAK Reporter
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