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.
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 nowA risk-based approach to LIMS project management is most commonly used. By assessing the criticality of each area, the project can be tailored to provide more focus on high-risk functionality. Download Part Three of this Series here.
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.
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.
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.
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.
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.
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.
A risk-based approach to LIMS project management is most commonly used. By assessing the criticality of each area, the project can be tailored to provide more focus on high-risk functionality. Download Part Three of this Series here.
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.
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.
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 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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