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What Are the Main Types of Healthcare Incidents?

MedTrainer

Incident reporting is essential to maintain a healthcare organization’s compliance with state and federal regulations and reveal what are the main types of healthcare incidents. Incident reporting creates a culture of safety and allows healthcare organizations to seek continuous improvement in their care practices.

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Upcoming Healthcare Regulations and Their Impact on Healthcare IT

Healthcare IT Today

Just like nutritional information on food packaging, disclosures about what aspects of care are the product of generative AI versus what has human oversight can improve public trust. For something as important and as sensitive as healthcare, there are plenty of rules and regulations in place to protect both patients and organizations.

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Future Trends and Regulatory Challenges in Med Device

Dot Compliance

Medical device manufacturers continuously try to streamline operations, improve quality, and reduce costs while struggling with global supply chain disruptions. Many of the steps device manufacturers are taking today to improve quality management and supply chain resiliency are aligned with the U.S. The agency has allocated $21.6M

FDA 52
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The PACE Solution to Increasing Demands for Long-Term Services and Supports in the U.S.

Healthcare Law Blog

PACE offers the convenience of a comprehensive, integrated suite of healthcare services for the elderly population, such as adult day primary care, emergency services, home care, hospital care, meals, occupational therapy, social work counseling, and transportation to PACE centers for activities or medical appointments. [8]

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Health Provider News

Hall Render

ALABAMA American Family Care opens new health care center in Northeast Birmingham doctors secure $13.9M

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SQA Regulatory Surveillance Summary 3 | Monthly Update 2021

SQA

The focus includes strengthening the exchange of best practices between Member States to achieve Union-wide high-quality solutions, thereby unlocking the potential of innovation in health, and improving efficiency by avoiding the duplication of activities and optimizing the use of financial resources.

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SQA Regulatory Surveillance Summary | Monthly Update 2023 – July and August 2023

SQA

and Rodrigues & Florindo SaĂşde e Vida Ltda. During a visit to the establishments, evidence of the manufacture of herbal medicines without registration and with a fraudulent label was observed, as the materials were produced in an environment with inadequate hygiene and sanitary conditions. For a list of the products seized, click here.

FDA 40