Felippe Domingos

Felippe Domingos

Felippe Domingos is a chemical engineer and Co-Founder of Actiz, a company that offers the most advanced LIMS in Latin America to optimize laboratory management with a focus on efficiency and cost reduction. With more than 200 projects in sectors such as pharmaceuticals, food, and petrochemicals, Felippe has built extensive experience in implementing LIMS systems.In 2020, after a request from an oil industry company in Colombia, he founded Actiz — a modern and accessible solution specially developed to address the challenges faced by laboratories in Latin America. Today, Actiz is present in four countries, serving segments such as food, biotechnology, and environmental analysis.Felippe shares his insights on laboratory automation and digitalization on LinkedIn. Connect with him to learn more about the future of laboratories with LIMS.

Laboratory Quality Management Software: How to Compare Your Options in 2026

Software de gestão da qualidade para laboratório: profissional analisando amostras

Choosing a laboratory quality management software involves comparing four types of solutions: spreadsheets, in-house built systems, ERP quality modules, and dedicated LIMS platforms. Each category addresses different needs in terms of traceability, regulatory compliance, and scale — there's no one-size-fits-all answer, but there is a right solution for your lab's current stage.

Poor Reagent and Expiration Date Management

Profissional com luvas de proteção manuseando frascos e tampas de reagente em linha de envase.

Inadequate reagent and expiration date management undermines the reliability of laboratory results, increases the risk of nonconformities, and hampers traceability. Learn how to structure an efficient process and how a Laboratory Information Management System (LIMS) strengthens control over reagent stock, expiration dates, and usage.

Manual and Inconsistent Laboratory Records

Analista de laboratório anotando dados manualmente em prancheta, registros laboratoriais manuais.

Manual and inconsistent laboratory records pose a critical risk to data integrity, undermining traceability, compliance, and analytical reliability. Standardizing documentation, combined with a Laboratory Information Management System (LIMS), reduces transcription errors, strengthens audits, and ensures greater control over laboratory information.

Inadequate Investigation of Out-of-Specification (OOS) Results

Analista com EPI completo investigando amostra com lupa, investigação de OOS.

Out-of-specification (OOS) results require structured, traceable, root-cause-driven investigations. Failures in this process compromise data integrity, increase regulatory risk, and can lead laboratories to incorrect technical decisions. Supported by a Laboratory Information Management System (LIMS), laboratories can strengthen traceability, standardize investigations, and ensure greater analytical reliability.