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LabHQ Pushes Pharmaceuticals Further

Simplify pharmaceutical lab testing whilst driving efficiencies. Automate workflows, ensure compliance and accelerate drug development.

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Meeting Pharmaceutical Industry Demands

Facing strict regulations on product safety, efficacy, and quality is challenging. For highly regulated pharma labs, maintaining traceability and audit trails for samples and batches—while avoiding data integrity issues—is complex, especially when both turnaround times and quality are critical. LabHQ is purpose-built to meet these demands, helping labs stay compliant while streamlining workflows and ensuring data integrity.

Features for the Pharma Industry

Features for the Pharma Industry

LabHQ LIMS tackles common pharma lab challenges head-on with features built & validated for the pharmaceutical industry.

Sample tracking

Track samples from submission to approval, store data digitally, eliminate manual errors, and enjoy smoother workflows.

Sample batching

Batch samples to boost efficiency, optimize resources, maximize utilization, and minimize downtime.

Custom fields

Capture unique data points and define custom data fields. Add, modify, or remove as needed to match your lab's evolving needs.

Certificate of analysis

Generate certificates with a click, reduce errors, speed up turnaround, tailor templates, and stay compliant.

We are often inspected by FDA and MHRA to GMP regulations and by UKAS to maintain and continuously develop our schedule of accreditation. LabHQ facilitates our adherence to data integrity regulatory standards such as FDA 21 CFR Part 11 and ISO 17025.

Lynne Hassel
Quality Director, Broughton

LabHQ Solutions for the Pharmaceutical Industry

LabHQ keeps your lab compliant, efficient, and ahead of the game with features validated for the fast-moving and highly regulated pharmaceutical industry.

Data Security and Integrity

Lock in accuracy and security with automated entry, validation, and audit trails.

Quality Assurance

Implement and monitor quality control measures to ensure all processes meet stringent standards.

Automate Compliance

Automate documentation and validation to ensure compliance with FDA, EMA, MHRA, and GMP standards.

Enhanced Sample Management

Track samples accurately through every stage of testing, ensuring consistent and reliable results.

Regulatory Compliance

Easily meet FDA, EMA, MHRA, and GMP standards with features designed for comprehensive documentation and reporting.

Enhanced Traceability

Audit trails enhance traceability, making it easy to track every sample and batch.

Security and compliance in our DNA

Built for quality, compliance, and peace of mind by a team with decades of QC and GxP experience in highly regulated industries.

FDA 21 CFR Part 11

Stay compliant with FDA 21 CFR Part 11 by maintaining secure, trackable electronic records and signatures.

GMP & GLP

Adhere to Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP) to ensure safe products through strong quality control (QC), clear documentation, and consistent, reliable non-clinical lab data.

MHRA

Meet MHRA guidelines and protect patient data with HIPAA compliance for data safety.

HPRA

Stick to Health Products Regulatory Authority (HPRA) standards for quality and safety in lab testing.

ISO 17025

Support ISO 17025 certified with validated testing methods and accurate, traceable lab results.

ISO 9001

Think of it as the blueprint for quality management. ISO 9001 ensures consistent, high-quality outputs and helps maintain trust with customers and stakeholders.

Take LabHQ for a test drive!

Explore our interactive demo & get a feel for LabHQ - in your own time and at your own pace.

Unsure of your LIMS requirements?

Use our quick Requirements Mapper to identify exactly what your lab needs in just a few minutes.

What is a LIMS in pharma?

A LIMS in pharma is a software solution designed to manage data, streamline workflows, and ensure compliance with regulatory standards in pharmaceutical laboratories.

Is LIMS GMP compliant?

Yes, pharmaceutical LIMS can be Good Manufacturing Practice (GMP) compliant. LabHQ makes sure that all processes and data management practices meet GMP standards.

Are there specific considerations in selecting a pharmaceutical LIMS?

Yes, key considerations include compliance with regulatory standards, data integrity, user management, and the ability to integrate with existing lab systems. LabHQ has made sure we meet all of these criteria, so you don’t have to worry. 

Latest from LabHQ

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How to Choose the Right LIMS for Your Lab

Choosing the right Laboratory Information Management System (LIMS) can feel overwhelming, but it doesn't have to be. This article is designed to empower lab managers and owners by offering practical tips for evaluating LIMS solutions. You'll discover how to prioritize factors like ease of use, scalability, compliance, and cost while addressing common fears such as configuration pitfalls or long-term scalability. By the end, you'll see why a LIMS tailored to your needs, like LabHQ, is essential for driving efficiency, ensuring compliance, and preparing your lab for growth.

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Industries progressing with LabHQ

From pharmaceuticals to textiles, LabHQ simplifies sample management and levels up lab performance across industries.