LIMS
LIMS

Laboratory Management System (LIMS)

Digitize your laboratory workflow and optimize the management of samples, tests and results with a secure, validated solution that is fully integrated into the quality system.

What is LIMS?

Laboratory Management System

Verifarma LIMS is a solution designed to automate, control and document all pharmaceutical laboratory activities, ensuring data integrity and compliance with international regulations. The system allows us to manage the complete cycle of samples —from their entry to the issuance of results—optimizing laboratory processes, reducing manual errors and improving response times.

Routine Analysis

Manage quality control by defining protocols and tests, assigning analysts, and issuing automated certificates of analysis (COA).

Stability

Manage stability studies, defining strategies and storage conditions, monitoring results and generating evolution reports.

Sample Management

Control the entire life cycle of samples through coding, traceability, location and automatic report generation, with direct integration with routine, calculation and stability modules.

Calculations

Automate the verification and approval of analytical calculations, automatically generating reports and validating results to ensure data integrity.

Get to know LIMS in operation
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Our AI solution

When quality becomes intelligent

Vera joins our product to transform quality data into actionable information, improving efficiency and operational control.

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Why choose Verifarma?

With more than 16 years of experience, we support life science in complying with traceability regulations in Latin America, Europe and other markets.

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Increased control and security

Electronic signature and Audit Trail. Cloud solution with a focus on data integrity. Full traceability of information. Notification and alert system.

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Specialization in the industry

21 CFR Part 11 compliance. Validable solution under GAMP 5 — Category 4. Platform ready to adapt to regulatory changes. Specific design for the pharmaceutical industry.

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Time and cost savings

Paperless operation. Agile access to information. Greater speed and efficiency in operational processes.

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Accessible, comprehensive and collaborative

24/7 technical support. Cross-cutting platform that connects multiple areas of the organization. Remote access from any location. Intuitive and easy to use interface.

Pharmaceutical industry trust

Change the drop for: More than 2000 companies trust Verifarma to ensure patient safety.

ISO 9001/ISO 27001
Quality and safety management.
GAMP 5
Validatable software
GS1 logo with stylized white curved lines on a blue circle background.
GS1
Meeting standards since 2008
FDA Certified Compliance seal.
FDA 21 CFR Part 11
FDA compliance and digital signatures
Blue circular badge with text EU COMPLIANT and Annex 11.
EU ANNEX 11
Compliance with EU guidelines
Reliable, validated technology for regulated and demanding environments.

Reviews from our customers

“Meiji decided to trust Verifarma to modernize the processes that existed on paper, improve data integrity and facilitate digital and remote work.”

Marta Palencia
Quality Assurance, Tedec Meiji

“I am extremely satisfied with Verifarma's document management system. With their help, I can access all my critical documents efficiently and securely from anywhere. I appreciate that they have adapted to my quality system.”

Agustin Kanashiro
Co-Chief Technical Officer, Ferring Pharmaceuticals

“We have implemented Verfarma Integrated Solutions to improve the efficiency, security and accessibility of our files, optimizing search, storage and collaboration processes, thus ensuring more effective and organized document management”

Sebastian Cembal
Responsible Pharmacist Deputy, Varifarma
The opinion of our customers supports us
Success stories tested.
Real experiences of our customers.
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Learn how our solutions can adapt to your processes and regulatory requirements. Our team will accompany you for a personalized demonstration.

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