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Australia: Musculoskeletal Burden and Opportunities for Orthopedic Device Growth – February/March 2026

Australia: Musculoskeletal Burden and Opportunities for Orthopedic Device Growth – February/March 2026

  • 2026-04-01 01:58:24

Musculoskeletal (MSK) conditions are a major health burden in Australia, ranking among the top 5 contributors to overall disease burden in 2024 and affecting nearly 7.3M people. Rising prevalence, aging demographics, and significant healthcare spending are driving growing demand for orthopedic technologies. As advanced solutions such as surgical robotics, smart implants, and regenerative therapies gain adoption, Australia's orthopedic sector continues to expand with increasing demand for innovative medical technologies.

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Qualtech Webinar: Navigating Medical Device Studies in the US - Regulatory Strategy, Study Design, and Subject Management - March 2026

Qualtech Webinar: Navigating Medical Device Studies in the US - Regulatory Strategy, Study Design, and Subject Management - March 2026

  • 2026-03-04 08:36:52

Join Qualtech's free webinar, "Medical Device Studies in the US: Regulatory Requirements, Study Design, and Best Practices in Subject Management" on March 26, 2026. This complimentary session is designed to provide clear and practical insights into US regulatory expectations, study design considerations, and effective subject management strategies.

Take advantage of this opportunity to strengthen your understanding of US medical device study requirements

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Australia: Artificial Intelligence (AI) is Transforming Australian Healthcare – October/November 2025

Australia: Artificial Intelligence (AI) is Transforming Australian Healthcare – October/November 2025

  • 2025-11-26 08:01:00

Artificial Intelligence (AI) is rapidly transforming healthcare in Australia, offering innovative solutions to meet the growing demands of an aging population and chronic disease management. With the AI healthcare market projected to reach AUD 1.78 billion by 2030, AI's potential to enhance early diagnosis and optimize treatments is substantial. Despite challenges like data fragmentation and regulatory complexities, AI is set to revolutionize healthcare delivery across the country.

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Malaysia: A Dental Powerhouse, A Health Puzzle – August/September 2025

Malaysia: A Dental Powerhouse, A Health Puzzle – August/September 2025

  • 2025-09-24 10:06:53

Malaysia has emerged as a dental powerhouse, attracting international patients with world-class treatments at affordable prices, while fueling one of ASEAN's fastest-growing dental device markets. With over 3,700 private clinics and a nationwide network of public facilities, the country is well-positioned to meet rising demand driven by medical tourism and a tech-savvy private sector. Yet, Malaysia also faces a domestic oral health challenge, highlighting both the urgency and the opportunity for innovation.

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QT ACTIVITY: Entering Japan & South Korea – Understanding PMDA & MFDS Requirements for Medical Devices WEBINAR RECAP - AUGUST/SEPTEMBER 2025

QT ACTIVITY: Entering Japan & South Korea – Understanding PMDA & MFDS Requirements for Medical Devices WEBINAR RECAP - AUGUST/SEPTEMBER 2025

  • 2025-09-24 09:35:21

On September 4, 2025, Qualtech hosted a webinar focusing on the medical device regulatory landscapes of Japan and South Korea. Led by our Japan and South Korea Registration Team Leaders, the session offered participants a structured overview of both markets, covering regulatory frameworks, registration pathways, and key updates shaping compliance today.

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SOUTH KOREA: AMENDMENT TO THE MEDICAL DEVICE ENFORCEMENT RULES AND MEDICAL DEVICE STANDARDS - AUGUST/SEPTEMBER 2025

SOUTH KOREA: AMENDMENT TO THE MEDICAL DEVICE ENFORCEMENT RULES AND MEDICAL DEVICE STANDARDS - AUGUST/SEPTEMBER 2025

  • 2025-09-24 08:47:47

The Ministry of Food and Drug Safety (MFDS) has announced amendments to both the Enforcement Rules of the Medical Device Act and the Medical Device Standards. The revisions, implemented between April and August 2025, included higher fees for innovative medical device reviews, exemptions from documentation requirements, stricter administrative sanctions, and the establishment of long-term follow-up requirements. In addition, amendments to the Medical Device Standards have been finalized and are scheduled to take effect in July 2026, introducing new standards and aligning existing ones with international norms.

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USA: Marketing Submission Recommendations for a Predetermined Change Control Plan for Artificial Intelligence-Enabled Device Software Functions - August/September 2025

USA: Marketing Submission Recommendations for a Predetermined Change Control Plan for Artificial Intelligence-Enabled Device Software Functions - August/September 2025

  • 2025-09-24 07:20:49

The FDA has issued draft guidance on marketing submissions for AI-enabled device software functions (AI-DSFs), with a focus on using a predetermined change control plan (PCCP). A PCCP allows manufacturers to plan and manage software changes in a predictable and controlled way, making regulatory review smoother and device performance more reliable.

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AUSTRALIA: Beauty Obsession in AUSTRALIA: Cosmetic Procedures on the Rise – JULY/AUGUST 2025

AUSTRALIA: Beauty Obsession in AUSTRALIA: Cosmetic Procedures on the Rise – JULY/AUGUST 2025

  • 2025-08-25 08:41:48

Australia's aesthetic market is entering a high-growth phase, with nearly 7 million adults considering cosmetic surgery and industry value projected at US$1.5 billion in 2024. Strong demand for injectables and advanced devices, supported by new national standards, offers aesthetic medical device manufacturers strong potential to introduce innovative solutions and capture growth in this dynamic market.

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