Highlights
- What a quality manager does, the main responsibilities of the role, common day-to-day challenges, and how a LIMS makes it easier to ensure compliance and traceability.

Learn how ISO 17025 ensures quality, technical competence, and credibility, and how a LIMS helps laboratories maintain regulatory compliance.

On July 3, 2023, the Brazilian Association of Technical Standards (ABNT) published the long-awaited update to Standard NBR 14725, replacing the former FISPQ (Chemical Product Safety Information Sheet) with the FDS (Safety Data Sheet).

Equipment qualification is a critical process to ensure that equipment used in industrial and laboratory processes meets specified requirements.

Understand the difference between qualification and validation in the pharmaceutical industry and learn how LIMS supports compliance and safety.

Discover how Good Manufacturing Practices (GMP) and a LIMS work together to ensure quality, safety, and regulatory compliance in the pharmaceutical industry.

Learn everything your quality control laboratory needs to consider when comparing LIMS solutions and what it takes to choose the right one.

Understand the principles of Good Laboratory Practice (GLP) and how a LIMS for quality control laboratories can help reinforce them.

Learn everything about batch control and how a LIMS can help you keep it organized within your laboratory.

Understand the role barcodes can play in meeting traceability requirements within your laboratory.

Learn the key differences between a LIMS system and a LIS system, and find out which one is the right fit for your organization.

Understand what computer system validation is, which systems you need to validate, and how to apply this process in your company.

Learn everything about LIMS systems in this article, including what it is, how it works, the difference between LIMS and LIS, and why your laboratory needs one.