MedTrainer

APRIL 5, 2021

Document Management Solutions for Regulatory Compliance. Document Management Solutions for Regulatory Compliance. Many institutions rely on paper copies to manage their organization’s information, particularly regarding compliance issues. grew: Record-Keeping and Reporting.

Regulatory Compliance 40

Regulatory Compliance Compliance Records Management Doctors 40

MedTrainer

AUGUST 1, 2024

Compliance audits are critical to healthcare management, ensuring that healthcare organizations adhere to legal and regulatory standards. Audits help identify areas of non-compliance, mitigate risks, and support high standards of patient care and data security. What is a Healthcare Compliance Audit?

Compliance 52

Compliance Regulations Compliance Patient Satisfaction Governance 52

Healthcare IT Today

APRIL 15, 2024

Through this acquisition, Access significantly accelerates its entry into the electronic health records (EHR) and archival digital records management markets, which are closely aligned with its robust records archiving and compliance management capabilities. Access has been named 12 times to the Inc.

Records Management 75

Records Management Compliance Governance Hospitals 75

Compliancy Group

SEPTEMBER 13, 2023

In the complex and dynamic world of healthcare, managing risk is essential to ensure patient safety and protect organizations from potential litigation or non-compliance. Schedule a Demo See the software that makes compliance management a breeze!

Records Management 52

Records Management Compliance HIPAA Health Insurance 52

Compliancy Group

DECEMBER 9, 2024

Carelessly discarding healthcare documents leaves protected health information (PHI) vulnerable. Non-compliance with Health Insurance Portability and Accountability Act (HIPAA) shredding requirements puts patients, employees, and your organization at risk for privacy breaches, fraud, and other threats.

HIPAA 52

HIPAA Compliance Records Management Fraud 52

Healthcare IT Today

MARCH 15, 2023

The number of stakeholders in charge of this field has multiplied (CIO, CDO, CTO, business leaders, records manager, data protection officer, compliance officer, office manager, etc.) and they must all operate from one information security framework that ensures compliance, protection and interoperability.

Compliance 110

Compliance Governance Compliance Officers Records Management 110

Dot Compliance

JANUARY 7, 2025

Electronic Quality Management Systems (eQMS) help meet these demands by streamlining processes, helping to meet compliance, and supporting continuous improvement across the enterprise. Nonconformance Management Incident reporting: Facilitate the timely reporting and investigation of nonconformities, deviations, and complaints.

Medical Device Industry 59

Medical Device Industry Regulatory Compliance Compliance FDA 59

Dot Compliance

MARCH 17, 2022

All while keeping in mind that compliance to regulations and global standards are non-negotiable, especially in the highly regulated life science and biotech industries. Here are key points to consider when selecting a QMS solution to support your company’s compliance and growth.

Regulatory Compliance 52

Regulatory Compliance Compliance Records Management FDA 52

Dot Compliance

DECEMBER 7, 2022

Quality Management System Examples 4. Dot Compliance eQMS Essential Elements 5. Ensuring Compliance with ISO 9001, EU MDR, FDA & More 6. Quality Management System Development 7. What is Quality Management System (QMS)? An international standard for Quality Management systems is ISO 9001:2015. (or

FDA 52

FDA Compliance Records Management 52

Total Medical ComplianceHIPAA

NOVEMBER 13, 2023

Develop a documented process for managing exceptions to information requests, aligning them with consent, privacy, and regulatory requirements. Develop a documented process for managing exceptions to information requests, aligning them with consent, privacy, and regulatory requirements.

Records Management 52

Records Management Hospitals Compliance HIPAA 52

SQA

OCTOBER 18, 2024

Three levels of regulatory confidence are defined in the regulation that are based on documents from the PIC/S reliance working group: Level 1: When a complete analysis of the inspection report or equivalent document of EFRA is performed to evaluate the service to GMP requirements and can be adopted unilaterally by ANVISA.

FDA 52

FDA Compliance Public Health World Health 52

SQA

OCTOBER 18, 2024

Three levels of regulatory confidence are defined in the regulation that are based on documents from the PIC/S reliance working group: Level 1: When a complete analysis of the inspection report or equivalent document of EFRA is performed to evaluate the service to GMP requirements and can be adopted unilaterally by ANVISA.

FDA 40

FDA Compliance Public Health Governance 40

SQA

JUNE 3, 2024

The document guides health and health surveillance professionals on the Resolution of the Collegiate Board (RDC) 339/2020, which established the National Biovigilance System. The DSVG documents aim to harmonize vigilance reporting for manufacturers of these specific devices.

FDA 40

FDA COVID-19 Licensing Nurses 40