EDUCATIONAL LITERATURE

RESOURCES / Educational Literature

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

LabHQ LIMS Leaflet

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

View 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

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 the LabHQ LIMS Stability Study Management module can control protocols, schedule time-points ensuring you never miss one and facilitate easy reporting and trending.

Download now

Equipment Maintenance

Are you struggling to keep your equipment fit for purpose?

Download this leaflet to learn how the LabHQ LIMS 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.

Download now

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 the LabHQ LIMS Stock Management module.

Download now

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.

Download now

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

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

A Sample Lifecycle in 7 Easy Steps

LabHQ LIMS Preview.

Get a glimpse on how easy it is to use LabHQ LIMS!

View now

GxP Compliant Project Checklist

Ensure your next GxP compliant project runs smoothly.

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. The omission of a required deliverable could jeopardise quality. Producing an unrequired deliverable creates undue work and slows the project down. Download our complimentary checklist to start preventing errors today.

Download now

Creating a Culture of Quality for Data Integrity in a Business - White Paper

As of 2015, the MHRA has imposed stricter policies on the pharmaceutical industry to be more proactive in its efforts at data integrity.

Data integrity is a fundamental component in a quality pharmaceutical system, ensuring that medicines are safe and effective. To satisfy the changes to MHRA regulatory requirements, pharmaceutical companies must continuously improve to create a Culture of Quality. Don't delay - download our complimentary white paper on how to implement a Culture of Quality for Data Integrity in a Business.

Download now

Best Practices: Meeting Client Expectations - Infographic

Don't lose sight of your primary goals.

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

Ensure your next GxP compliant project runs smoothly.

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. The omission of a required deliverable could jeopardise quality. Producing an unrequired deliverable creates undue work and slows the project down. Download our complimentary checklist to start preventing errors today.

Download now

Creating a Culture of Quality for Data Integrity in a Business - White Paper

As of 2015, the MHRA has imposed stricter policies on the pharmaceutical industry to be more proactive in its efforts at data integrity.

Data integrity is a fundamental component in a quality pharmaceutical system, ensuring that medicines are safe and effective. To satisfy the changes to MHRA regulatory requirements, pharmaceutical companies must continuously improve to create a Culture of Quality. Don't delay - download our complimentary white paper on how to implement a Culture of Quality for Data Integrity in a Business.

Download now

Best Practices: Meeting Client Expectations - Infographic

Don't lose sight of your primary goals.

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

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

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

Ensure your next GxP compliant project runs smoothly.

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. The omission of a required deliverable could jeopardise quality. Producing an unrequired deliverable creates undue work and slows the project down. Download our complimentary checklist to start preventing errors today.

Download now

Creating a Culture of Quality for Data Integrity in a Business - White Paper

As of 2015, the MHRA has imposed stricter policies on the pharmaceutical industry to be more proactive in its efforts at data integrity.

Data integrity is a fundamental component in a quality pharmaceutical system, ensuring that medicines are safe and effective. To satisfy the changes to MHRA regulatory requirements, pharmaceutical companies must continuously improve to create a Culture of Quality. Don't delay - download our complimentary white paper on how to implement a Culture of Quality for Data Integrity in a Business.

Download now

Best Practices: Meeting Client Expectations - Infographic

Don't lose sight of your primary goals.

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.

Download now

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.

Download now

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.

Download now

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.

Download now

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.

View now

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!

View now
 

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!

View now