LabHQ Pushes Pharmaceuticals Further
Simplify pharmaceutical lab testing whilst driving efficiencies. Automate workflows, ensure compliance and accelerate drug development.
Meeting Pharmaceutical Industry Demands
Facing strict regulations on product safety, efficacy, and quality is challenging, and maintaining traceability and audit trails for samples and batches while avoiding data integrity issues is complex for highly regulated pharma labs where both turnaround times & quality are critical.
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.
LabHQ Solutions for the Pharmaceutical Industry
LabHQ keeps your lab compliant, efficient, and ahead of the game with features validated for the fast-moving & 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 for 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
Get ISO 17025 certified with validated testing methods and accurate, traceable lab results.
ISO 9001
Maintain ISO 9001 standards for quality management systems ensuring consistent, high-quality outputs.
FAQs
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.
