How LIMS Simplifies Audits and Accreditations
Discover how a LIMS simplifies audits and accreditations, ensures data traceability, standardizes processes, and strengthens compliance.
Standards and Practices
Risk Management in Laboratories: How LIMS Strengthens Compliance and Reliability
Understand why risk management is essential and how a LIMS can turn risk into efficiency and compliance for your laboratory. Find out more.
Smart Non-Conformity Management: From Theory to Practice with Technology
Optimize non-conformity and corrective action management in your laboratory with the support of a LIMS system. Learn more on the Actiz blog!
RDC 48/13 and LIMS: What Are Good Manufacturing Practices for Cosmetics and Personal Care Products
RDC 48/13 sets out Good Manufacturing Practices for cosmetics in Brazil. Learn how a LIMS helps your company ensure regulatory compliance and operational excellence.
Good Laboratory Practice (GLP): What It Is and Why It Is Essential
Understand what Good Laboratory Practice (GLP) is, why it matters, and how a LIMS helps ensure quality, traceability, and compliance.
Rising Recalls in the Food and Beverage Industry: How to Minimize Risk with Sound Management Practices
Discover the key precursors driving the rise in food and beverage recalls and how a LIMS can help mitigate them.
RDC 318/2019: How to Conduct Stability Studies for Pharmaceutical Ingredients and Medicines with a LIMS
Learn about RDC 318/2019 and discover how a LIMS can ensure compliance, safety, and efficiency in stability studies for pharmaceutical ingredients.
RDC 47/13 and LIMS: How to Apply Good Manufacturing Practices for Sanitizing Products
Understand RDC 47/13 and how to apply Good Manufacturing Practices for sanitizing products using technology, training, and an efficient LIMS system.
External Audit: How a LIMS Can Help With Preparation and Compliance
Discover how to prepare your laboratory for audits with greater confidence using a LIMS. Learn more on the Actiz blog!
How to Comply with ANVISA’s RDC 658/22: Good Manufacturing Practices, LIMS, and the Path to Compliance
Discover how ANVISA's RDC 658/22 impacts the pharmaceutical industry and how a LIMS can ensure compliance and efficiency.
How to Map Laboratory Risks with a LIMS and Turn Challenges into Opportunities?
Discover how to implement risk management in laboratories and see how a LIMS can drive operational excellence. Find out now!
The Importance of LIMS for ISO 17025 Compliance
In laboratory environments, fast decision-making is often required and must be based on reliable data — analytical results, quality assurance information, environmental pollutant measurements, and product specification checks. Achieving that reliability at scale depends on consistent, traceable processes across every stage of lab operations, which is exactly where a LIMS becomes essential for ISO/IEC 17025 compliance.