Many laboratories introduce LIMS to help with sample data management and reporting. Some labs will have used the same system for 12 years without upgrades, and other labs will
Theresa Webster
Recent Posts
4 Signs Your Lab Has Outgrown Your LIMS
by Theresa Webster posted in LIMS, Data Management, Data Integrity, Process Improvement, process mapping, QC Laboratory Data Management, QualityThe Best LIMS Features for Quality
by Theresa Webster posted in LIMS, Data Management, Data Integrity, QC Laboratory Data Management, QualityThe purpose of quality is to ensure standards are maintained so that products, services and processes are effective and fit for purpose. Laboratories must maintain high quality standards to provide confidence in
What the Regulators are Looking for in a LIMS Validation Plan
by Theresa Webster posted in LIMS, Data Integrity, Project Management, Process ImprovementValidating LIMS is a fundamental requirement for GMP compliance. Where LIMS is used to store and process GMP data, it is imperative that
Why Most Laboratories are Switching to Cloud Computing
by Theresa Webster posted in LIMS, Project Management, Process Improvement, Return on Investment,
The concept of cloud computing has actually been around since the 1960s, and it wasn’t until 2006 that it started to gain traction in industry. In contrast to the cloud,
I Want LIMS But Don't Have Time to Deploy It
by Theresa Webster posted in LIMS, Project Management, Process Improvement, Return on Investment,
Laboratories are fast-paced environments where accuracy and turnaround time is critical, especially for Quality Control labs. Delivering results and meeting customer expectations is paramount, and where
Computerised Systems: A Summary of 2016 MHRA Inspections
by Theresa Webster posted in Data Integrity, audits, MHRA, GMP requirementsThe Medicines and Healthcare products Regulatory Agency (MHRA) has a responsibility to protect public health by ensuring that medicines and medical devices meet applicable standards of safety, quality and efficacy. Each year, they conduct
Is My Audit Trail Regulatory Compliant?
by Theresa Webster posted in LIMS, Data Integrity, audits, FDA, MHRA, GMP requirementsOperating a laboratory within regulatory requirements can be a challenge. The wording of regulations is typically cryptic, and there’s always room for different interpretations. Audit trails are an important factor for compliance because
The Best LIMS Features for Improving Laboratory Productivity
by Theresa Webster posted in LIMS, Project Management, Process Improvement, process mappingFrom our experience of deploying LIMS systems within multiple facilities, we have compiled this list of the best LIMS features that have given
How to Choose the Right LIMS for Your Lab
by Theresa Webster posted in LIMS, Data Management, Project Management, Process ImprovementWith so many systems to choose from, how do you select the right LIMS for your lab? Below are some helpful words of advice to get you started on your journey of finding a LIMS.
How to Avoid Customer Complaints: Where LIMS Can Help
by Theresa Webster posted in LIMS, Data Management, Client Expectations, Project Management, Process Improvement, customer satisfactionDelivering on customer expectations is a shared and common goal for laboratories. Whether they are internal or external to your organisation, delighting customers is the ultimate reward for your work. Even when you have documented, implemented and trained procedures,