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.
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.
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.
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.
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.
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
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.
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.
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.
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.
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.
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.
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.
Looking to gain accreditation to ISO 17025? LIMS can often facilitate compliance to this standard, and here, you can download our free reference guide on how our flagship product, LabHQ LIMS, helps laboratories comply with specific areas of the standard.
Many laboratories who consider implementing LIMS usually think about the benefits to the lab. This is usually improved turnaround times, improved compliance and increased efficiencies. Download our whitepaper to read how users outside the lab can also benefit from LabHQ LIMS.
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.
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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