EDUCATIONAL LITERATURE

RESOURCES Educational Literature

Understanding-the-process

LIMS Project Planning Series Part One: Understanding the Process

Planning is a fundamental step for any LIMS project. Process mapping, as a key part of planning, allows you to understand your current practice and helps you identify opportunities for improvement. Download Part One of this Series for a guide on how to understand your process.

Download now

LIMS PROJECT PLANNING SERIES PART TWO: IDENTIFYING USER REQUIREMENTS

Have you heard the old saying "Fail to plan and plan to fail"? Effectively gathering User Requirements allows you to implement a LIMS that best suits your laboratory's needs. Download Part Two of this Series now.

Download now
book2

Essentials Toolkit: Calculating LabHQ LIMS Return on Investment

Compelling ROI figures will certainly support your justification for LIMS. Download our Essentials Toolkit below for an easy step by step instruction on how to calculate LabHQ LIMS return on investment.

Download now
how-to-choose-bookthumbnail

How to Choose Your Next Laboratory Improvement Project

Need to meet a business objective? Laboratory improvement projects are a great way to nurture collaboration and improve ways of working. Download our complimentary white paper to get started on your next improvement project today.

Download now

How LabHQ LIMS Addresses the Requirements of the FDA 21 CFR Part 11

Looking for a LIMS system that you can be sure meets the FDA 21 CFR part 11 requirements? See how this is achieved with LabHQ LIMS.

Download now

21 CFR Part 11 Electronic Records & Signatures Checklist

When it comes to remaining compliant with the FDA's 21 CFR part 11, use our easy-to-use checklist to help you get started on creating a LIMS User Requirements Document.

View now

SlideShare: Data Integrity - The End of 2017 Deadline

Data Integrity - Learn what the MHRA say you need to do before the end of 2017 to ensure regulatory compliance.

View now

Root Cause Analysis (RCA) Pocket Guide

Busy QC Laboratories are often under pressure to investigate the root cause of a problem and identify solutions to prevent recurrence. To do this they must rely on accurate data and sound methodology. Find out how this simple 5 step approach to RCA can help you.

Download now

The 5S Pocket Guide

Reduce waste and optimize productivity. This lean method encourages workers to improve their working conditions and helps them to learn to reduce waste, unplanned downtime, and in-process inventory. Find out how the 5S pillars can help your laboratory.

Download now

Want to know how LIMS generates a return on investment?

LIMS helps regulated industries such as pharmaceuticals in many ways. From regulatory compliance to product test data analysis and efficiency gains. Download our white paper to learn more about the benefits of using a LIMS.

Download now

ALCOA Pocket Guide

Data Integrity is fundamental good practice for all QC Laboratories. "ALCOA" principles remain a guiding tool for quality compliance. Find out what each of the acronyms in "ALCOA" mean.

Download now

GxP Compliant Project Checklist

Determining the set of deliverables to produce for a given system is one of the key elements of planning. It is important to select the right subset of Computer Systems Validation Process (CSVP) deliverables. Download our complimentary checklist to help you plan a GxP LIMS project today.

Download now

Creating a Culture of Quality for Data Integrity in a Business

Data integrity is fundamental to a pharmaceutical quality system, ensuring that medicines are safe and effective. To satisfy the changes to MHRA regulatory requirements, companies must continuously improve to create a Culture of Quality. Download our white paper on how to implement a Culture of Quality.

Download now

Best Practices: Meeting Client Expectations - Infographic

Most businesses seek to nurture their relationships with clients, but successful businesses enchant their customers. Download our complimentary infographic on "The 7 Principles to Meet Client Expectations" and stay on task today

Download now

21 CFR Part 11 Electronic Records & Signatures Checklist

When it comes to remaining compliant with the FDA's 21 CFR part 11, use our easy-to-use checklist to help you get started on creating a LIMS User Requirements Document.

View now

SlideShare: Data Integrity - The End of 2017 Deadline

Data Integrity - Learn what the MHRA say you need to do before the end of 2017 to ensure regulatory compliance.

View now

Want to know how LIMS generates a return on investment?

LIMS helps regulated industries such as pharmaceuticals in many ways. From regulatory compliance to product test data analysis and efficiency gains. Download our white paper to learn more about the benefits of using a LIMS.

Download now

ALCOA Pocket Guide

Data Integrity is fundamental good practice for all QC Laboratories. "ALCOA" principles remain a guiding tool for quality compliance. Find out what each of the acronyms in "ALCOA" mean

Download now

GxP Compliant Project Checklist

Determining the set of deliverables to produce for a given system is one of the key elements of planning. It is important to select the right subset of Computer Systems Validation Process (CSVP) deliverables. Download our complimentary checklist to help you plan a GxP LIMS project today.

Download now

Creating a Culture of Quality for Data Integrity in a Business

Data integrity is fundamental to a pharmaceutical quality system, ensuring that medicines are safe and effective. To satisfy the changes to MHRA regulatory requirements, companies must continuously improve to create a Culture of Quality. Download our white paper on how to implement a Culture of Quality.

Download now

Best Practices: Meeting Client Expectations - Infographic

Most businesses seek to nurture their relationships with clients, but successful businesses enchant their customers. Download our complimentary infographic on "The 7 Principles to Meet Client Expectations" and stay on task today.

Download now
book2

Essentials Toolkit: Calculating LabHQ LIMS Return on Investment

Compelling ROI figures will certainly support your justification for LIMS. Download our Essentials Toolkit below for an easy step by step instruction on how to calculate LabHQ LIMS return on investment.

Download now

Want to know how LIMS generates a return on investment?

LIMS helps regulated industries such as pharmaceuticals in many ways. From regulatory compliance to product test data analysis and efficiency gains. Download our white paper to learn more about the benefits of using a LIMS.

Download now
Understanding-the-process

LIMS Project Planning Series Part One: Understanding the Process

Planning is a fundamental step for any LIMS project. Process mapping, as a key part of planning, allows you to understand your current practice and helps you identify opportunities for improvement. Download Part One of this Series for a guide on how to understand your process.

Download now
how-to-choose-bookthumbnail

How to Choose Your Next Laboratory Improvement Project

Need to meet a business objective? Laboratory improvement projects are a great way to nurture collaboration and improve ways of working.  Download our complimentary white paper to get started on your next improvement project today.

Download now
02-1

21 CFR Part 11 Electronic Records & Signatures Checklist

When it comes to remaining compliant with the FDA's 21 CFR part 11, use our easy-to-use checklist to help you get started on creating a LIMS User Requirements Document.

View now

Want to know how LIMS generates a return on investment?

LIMS helps regulated industries such as pharmaceuticals in many ways. From regulatory compliance to product test data analysis and efficiency gains. Download our white paper to learn more about the benefits of using a LIMS.

Download now

GxP Compliant Project Checklist

Determining the set of deliverables to produce for a given system is one of the key elements of planning. It is important to select the right subset of Computer Systems Validation Process (CSVP) deliverables. Download our complimentary checklist to help you plan a GxP LIMS project today.

Download now

Creating a Culture of Quality for Data Integrity in a Business

Data integrity is fundamental to a pharmaceutical quality system, ensuring that medicines are safe and effective. To satisfy the changes to MHRA regulatory requirements, companies must continuously improve to create a Culture of Quality. Download our white paper on how to implement a Culture of Quality.

Download now

Best Practices: Meeting Client Expectations - Infographic

Most businesses seek to nurture their relationships with clients, but successful businesses enchant their customers. Download our complimentary infographic on "The 7 Principles to Meet Client Expectations" and stay on task today.

Download now

Root Cause Analysis (RCA) Pocket Guide

Busy QC Laboratories are often under pressure to investigate the root cause of a problem and identify solutions to prevent recurrence. To do this they must rely on accurate data and sound methodology. Find out how this simple 5 step approach to RCA can help you.

Download now

The 5S Pocket Guide

Reduce waste and optimize productivity. This lean method encourages workers to improve their working conditions and helps them to learn to reduce waste, unplanned downtime, and in-process inventory. Find out how the 5S pillars can help your laboratory.

Download now

ALCOA Pocket Guide

Data Integrity is fundamental good practice for all QC Laboratories. "ALCOA" principles remain a guiding tool for quality compliance. Find out what each of the acronyms in "ALCOA" mean.

Download now

How LabHQ LIMS Addresses the Requirements of the FDA 21 CFR Part 11

Looking for a LIMS system that you can be sure meets the FDA 21 CFR part 11 requirements? See how this is achieved with LabHQ LIMS.

Download now

SlideShare: Data Integrity - The End of 2017 Deadline

Data Integrity - Learn what the MHRA say you need to do before the end of 2017 to ensure regulatory compliance.

View now

Stability Study Management

Effective stability study management is vital to ensure ongoing product integrity and safety.

Download this leaflet to learn more about the how our Stability Study Management module can control protocols, schedule time-points ensuring you never miss one and facilitate easy reporting and trending.

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Equipment Maintenance

Are you struggling to keep your equipment fit for purpose?

Download this leaflet to learn how our Equipment Maintenance Management module can help schedule QC equipment maintenance, capture service history and record equipment items used in a test to facilitate regulatory compliance.

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Stock Management

Interested in managing and testing your QC stock inventory, and recording stock used in a test to facilitate regulatory compliance?

Download this leaflet to learn more about our Stock Management module.

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Environmental Monitoring

Environmental Monitoring is crucial to ensure that products, facilities and water meet safety and efficacy standards for public health. Download this leaflet to learn about Broughton Software Environmental Monitoring software.

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LabHQ Hosted Services FAQ

Read our most frequently asked questions and get the answers you're looking for when it comes to keeping your data safe and confidential.

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A Sample Lifecycle in 7 Easy Steps

LabHQ LIMS Preview.

Get a glimpse on how easy it is to use our laboratory information management system!

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LabHQ LIMS Leaflet

LabHQ is a software system used to store, process, report and analyse QC test data. Learn about how our laboratory information management system can help your lab today!

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