Remove 2023-evaluation-management-coding-changes-part-2
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Spring Forward With 2024 Compliance Changes

MedTrainer

It’s that time of the year to check your records for 2023 compliance deficiencies and set your organization up for success in 2024. Review Recent Compliance Changes There is a major shift in compliance priorities toward addressing health inequities and improving access to quality healthcare services.

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SQA Regulatory Surveillance Summary | Monthly Update 2024

SQA

The action was held from 26 to 28 September 2023, at the city’s international entry points. ” If the product is prohibited in Brazil, a notice of infraction is drawn up for smuggling of goods (Article 334 A, item II, of the Criminal Code), which is then sent to the Public Prosecutor’s Office for criminal investigation.

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

SQA

The measure, adopted through Resolution – RE 2910/2023 , was made after the Agency was informed by the Sanitary Surveillance of Goiás about the occurrence of serious adverse events associated with the incorrect use of the products. In addition, it contains essential recommendations to avoid complications and protect public health.

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Preparing for the End of the Public Health Emergency

YouCompli

CMS Updates to beneficiary PHE waivers that matter to healthcare compliance Sharon Parsley, JD, MBA, CHC, CHRC, contributes regularly to the YouCompli blog. As a result, the COVID-19 public health emergency (PHE) declared under Section 319 of the Public Health Service act, is expected to end officially on May 11, 2023.

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SQA Regulatory Surveillance Summary | Monthly Update 2023 – March And April

SQA

ANVISA Resumes Inspections in the Area of Technovigilance, 29 March 2023 In partnership with local Health Surveillance, ANVISA technical teams carried out in March 2023 two (2) medical device manufacturer inspections with an aim to strengthen the monitoring of these products in Brazil, ensuring their safety, performance, and quality.

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SQA Regulatory Surveillance Summary | Monthly Update 2022 – September/October

SQA

The changes will serve to strengthen the country’s medical device registration regulations upon their effective date of 01 March 2023. China’s Center for Medical Device Evaluation (CMDE) Update Compliance Guidelines and Recommended Paths for Clinical Evaluation Paths for Certain Medical Devices, 25 July 2022. 30 of 2022.

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The Cobra Effect & Enforcing Compliance Standards

AIHC

Lessons Learned about Consequences & Incentives Submitted by the AIHC Education Department Introduction The Office of Inspector General has released the new General Compliance Program Guidance or “GCPG” in late 2023. Even well-meaning changes and upgrades to policies can make a previously compliant industry noncompliant.