Dot Compliance

JANUARY 29, 2025

Improved Compliance and Risk Management Regulatory compliance: eQMS solutions help organizations meet industry-specific regulations, such as FDA, ISO 9001 , and GMP, by providing built-in compliance features. Download our white paper, How to Choose an eQMS , for more.

Regulatory Compliance 59

Regulatory Compliance Compliance FDA HIPAA 59

Dot Compliance

JANUARY 14, 2025

By tracking nonconformances, corrective actions, and preventive measures, businesses can improve product quality and reduce the likelihood of recalls or regulatory issues. Regulatory Compliance: eQMS can help organizations meet industry-specific regulations, such as ISO 9001, FDA 21 CFR Part 11, and others.

Compliance 59

Compliance Regulatory Compliance FDA 59

Dot Compliance

JANUARY 7, 2025

Enhance compliance: Ensure compliance with FDA regulations, including CGMP and 21 CFR Part 11 , through automated compliance checks and audit trails. Enhance regulatory compliance: Comply with Good Laboratory Practices (GLP) and other relevant regulations.

Medical Device Industry 59

Medical Device Industry Regulatory Compliance Compliance FDA 59

Dot Compliance

OCTOBER 11, 2024

It helps ensure product quality, patient safety, regulatory compliance and more. Regulatory Compliance Adherence to regulatory requirements, such as those outlined by the FDA’s 21 CFR Part 820, is mandatory for pharmaceutical manufacturers. What’s the Big Deal about CAPA?

Pharmaceutical Industry 52

Pharmaceutical Industry Regulatory Compliance Compliance FDA 52

Dot Compliance

OCTOBER 11, 2024

It helps ensure product quality, patient safety, regulatory compliance and more. Regulatory Compliance Adherence to regulatory requirements, such as those outlined by the FDA’s 21 CFR Part 820, is mandatory for pharmaceutical manufacturers. What’s the Big Deal about CAPA?

Pharmaceutical Industry 52

Pharmaceutical Industry Regulatory Compliance Compliance FDA 52

Dot Compliance

FEBRUARY 23, 2024

The Evolution of Quality Processes Years ago, quality management professionals relied on using manual, paper-based systems for managing their quality processes. Their tasks included documenting quality processes, obtaining signatures from authorized individuals, and storing documents for regulatory compliance.

FDA 52

FDA Regulatory Compliance Compliance 52