Yes.  Whether you are looking for a single-user stand-alone LIMS, or a complete business solution for your corporate enterprise, LabHQ is completely scalable to fit within your business requirements and flexible enough to grow with your laboratory.

The security features of LabHQ incorporate functionality such as user permissions, minimum password strength and forced password changes.  In addition to the standard user name and password, our customers also have the option to use a one time password (OTP) token similar to those used by internet banks to add an extra layer of security. To ensure that your requirements are met the security functions are easily customisable by the system administrator.
All LabHQ data transferred via the web is protected with the highest level of SSL Encryption available so you are guaranteed complete security of your information.

If you require your LIMS to be integrated to your MRP or ERP system please contact us.  Our project teams would be delighted to discuss these options with you.

Yes. Our clients benefit from both a locally installed LIMS application to execute the key laboratory functions combined with the added advantage of laboratory data being fully accessible via the web.  Data is securely accessible wherever there is an internet connection anywhere in the world.

LabHQ has been specifically designed to be compliant with GxP regulations so can be used in highly regulated environments such as pharmaceutical and other life science industries.
LabHQ can also operate in a paperless environment, if required, and therefore its design features will help users achieve compliance with electronic records and electronic signature regulations e.g. CFR 21 Part 11.

No, not if you don’t choose to. We offer a range of optional support packages including full support with system administration and computer system validation.
The software can be purchased as a core package for those companies who would prefer to set-up LabHQ using in-house staff, inclusive of our full, free telephone support and training, or can choose for us to project manage the whole process for you.  We can set-up all test methods, suites, products, workbooks, reporting templates and specifications based on your requirements allowing you to concentrate on your core business activities.
In addition, we will offer a full computer software validation package taking away any hassle involved in validating the LabHQ LIMS.  We will offer a full validation pack of SOPs that can be implemented into any quality management system with ease, fully validate the software including all calculations and custom reports and offer continuous computer validation support including the validation of all future updates, new methods and products.

LabHQ has been designed so that it can be implemented into laboratory functions with minimal disruption. We have kept our system as simple as possible to minimise implementation time involved in the set-up and training of laboratory users thus reducing the burden on your internal IT and technical staff.  We aim to have you up and running within 48 hours.

In today’s competitive market evolving enterprises like laboratories are under continual increasing pressure to provide faster turnaround and superior deliverables for their clients. Implementation of a suitable LIMS will not only increase productivity and efficiency of your laboratory but also increases the accuracy of data produced.

• A LIMS simplifies key process such as sample registration, results calculation, approval and reporting
• Implementation of a suitable LIMS can help maintain compliance with complex GxP regulations.
• A LIMS reduces calculation and transcription errors
• A LIMS allows effective tracking of sample status
• Provides data reports (e.g. productivity and process capability) on demand

A Laboratory Information Management System (LIMS) is computer software that allows users to manage the flow of data through the laboratory from sample receipt to result presentation. With a suitable LIMS in place the user can more effectively trace and track all samples that are received, the tests performed on these samples, methods used and results generated.