2025 Medical Device Cybersecurity Trends: What Will Shape The Industry?
What will the industry face or achieve in 2025? These trends will be critical in medical device cybersecurity.
Hosted on MSN2d
OCT Medical Devices 2025: biggest regulatory requirement issues ‘start at the site level’
When conducting a clinical investigation, meeting regulatory requirements is predicated on factors such as the quality of ...
GlobalData on MSN2d
Six months “a very limited window” for medical device shortage flagging
Beta CEO Marcel Botha talks about the FDA’s plans for medical shortage notifications and how Trump’s policies may impact US ...
PharmiWeb11d
Navigating the Crucial Path of Medical Device Validation and Verification
IntroductionIn the rapidly evolving healthcare landscape, medical devices play a pivotal role in enhancing patient care and improving health outcomes. The road to getting these devices from concept to ...
Digital Health9d
MHRA issues guidance on medical device surveillance regulation
The MHRA has issued fresh guidance to help medical device manufacturers prepare for upcoming regulatory changes.
Medical Design and Outsourcing7d
FDA’s Tarver pushes for mandatory medical device shortage reporting
The FDA is urging Congress to implement mandatory medical device shortage reporting to address growing vulnerabilities in the ...
JD Supra8d
MHRA publishes guidance on to new UK medical device post-market surveillance requirements
The Medicines and Healthcare products Regulatory Agency (MHRA) has issued a suite of guidance specifically designed to help medical ...
JD Supra9d
Sunshine Act Compliance: How to Take Action to Meet Reporting Requirements and Avoid Costly Penalties
The clock is ticking for medical device and pharmaceutical companies to fulfill their obligations under the Physician ...
Healthcare Dive14d
Tarver warns that US device supply chain vulnerabilities could harm patients
The new director of the FDA’s device center contrasted a European rule with the lack of mandatory reporting requirements for ...
Resyca Receives Medical Device Regulation Certificate From TÜV SÜD
MDR Certification Strengthens Resyca’s Leadership in Soft Mist Drug-Device Combination Products ENSCHEDE, NL / ACCESS ...
Mena FN14d
Medical Device Industry Hails CDSCO Move On Stopping Refurbished Imports
argued that the healthcare security of the country is already compromised with about 70 per cent of the current medical device requirements being met through imports. These imports without any ...