December 4, 2019 - LIMS Master Data Best Practices Part 2: Extrapolation of Master Data from Your Current Records
As we mentioned in part 1 of our LIMS Master Data Best Practices series, master data is the core information that needs to be in place in the system in order for a LIMS to function as intended. It’s essential for all parts of the organization to agree on both the meaning and usage of master data. As such, effective master data configuration is critical to the success of any LIMS implementation and migration, not to mention your organization as a whole. Developers configuring master data in a new LIMS will need to determine what master data fields are needed and where to put them in the system. In order to do this, relevant business process workflows and data points must be identified and properly mapped in the system. In this part 2 blog of our Master Data Best Practices series, we will detail best practices for identifying and mapping your LIMS master data, along with an effective methodology to ensure your mapping exercise maximizes business value for your organization.[Read More]
December 4, 2019 - How can I tell if it’s worth investing in a LIMS?
Given that many organizations and their laboratories are looking to improve efficiency and reduce costs, it may seem self-evident that introducing a Laboratory Information Management System (LIMS) should help in achieving that aim. However, tangible evidence in the form of a projected Return on Investment (ROI) and business plan is frequently required. In addition, these can provide a basis against which success of the project can be measured. Autoscribe Informatics have just published an updated version of their popular white paper ‘Justifying the Purchase of a LIMS’. This is designed to help any organization develop a detailed, evidence based justification for investing in a LIMS. This updated version not only discusses the key factors to be considered in an ROI assessment, but also provides models and examples for how ROI may be calculated.[Read More]
December 4, 2019 - Why STEM Education is Important to the Future of Lab Informatics
The topic of this blog was occasioned by a recent calendar observation. November 8 is recognized in the United States as National STEM Day (or National STEAM Day). STEM is the acronym for science, technology, engineering, and math; STEAM is its extension when you include the arts. Educators around the country use the occasion to expose their students to STEM activities and to talk about potential career paths. The Society for Information Management provides information about a number of STEM-related activities specific to information technology.[Read More]
November 13, 2019 - Reducing the Cost of Computer Systems Validation Efforts Through Risk Assessment
Computerized systems have been widely adopted by the pharmaceutical industry and are frequently used for instrument control and data evaluation, documentation, transmission and archiving in laboratories. The FDA requires that all computer systems in regulated environments be validated in a documented process known as computer system validation (CSV). CSV serves to verify that a computerized system does exactly what it is designed to do in a consistent and reproducible manner. For regulatory compliance purposes, CSV confirms the accuracy and integrity of data created, modified, archived, retrieved and transmitted by a computer system in order to ensure product safety and effectiveness. Computer system validation is required when configuring a new system or making a change in a validated system (upgrades, patches, extensions, etc.). Depending on the complexity and functionality of computer systems, CSV can be a significant undertaking. Pharmaceutical companies have even been known to delay upgrading applications to avoid the validation effort required. In this blog, we will provide some tips on performing a risk-based CSV in order to dramatically lower the costs of validation efforts.[Read More]
November 13, 2019 - The Essential Capabilities of a 21st Century CHRO
Change is clearly a dominant theme in the 21st century. With modern trends like the digital revolution, globalization, talent shortages, greater workforce mobility, and a multigenerational workforce, long-established business models are facing disruption on many different fronts, and companies seeking to maintain competitive advantage must be more agile and flexible than ever before. One of the keys to business success in today’s volatile economic environment is attracting and retaining the best talent. As such, industry leading organizations are recognizing the importance of the role of HR leaders to their continued success. Once known for simply managing traditional personnel and administrative tasks, roles for Chief Human Resources Officers (CHROs) are evolving beyond siloed people initiatives.[Read More]
November 7, 2019 - Utilizing the BIOVIA ELN with Pipeline Pilot to Enhance R&D
The BIOVIA ELN is a crucial technology that works with Pipeline Pilot in a seamless fashion. Modern laboratory technologies such as Electronic Laboratory Notebooks (ELNs) and LIMS have made enormous amounts of data available to scientists in life science laboratories. Scientists that are recording, managing and archiving research data in paper notebooks and performing tasks manually simply cannot keep up with this deluge of data. These paper-based methods lead to scenarios where much collected data is siloed and never analyzed, while many experiments end up being needlessly repeated.[Read More]
October 30, 2019 - LIMS Master Data Best Practices Part 1: Defining the Terms
Globalization and outsourcing trends, along with technological advancements that have dramatically increased the volume, complexity and variety of data, have created significant data management challenges for modern scientific laboratories. Most laboratories have responded to these challenges by implementing a Laboratory Information Management System (LIMS) that automates business processes and data capture associated with laboratory workflows. With these systems comes vast amounts of data. Ensuring you are managing your LIMS Master Data properly begins with understanding the key terms LIMS implementations usually demand a substantial investment of time, money and resources, typically costing hundreds of thousands to millions of dollars and requiring hundreds of person days to accomplish. Failure of a LIMS project can be a huge waste of time and resources, and a financial disaster for the organization involved. As such, it is critical to get a LIMS implementation right the first time in order to preserve your return on investment. One important facet of any successful LIMS implementation and/or migration is the design and configuration of master data. In our experience, many companies involved in LIMS implementations tend to focus on software testing and configuration and put off dealing with master data until the end of the project. This is a huge mistake. Master data design and configuration is typically a much bigger job than anticipated and has multimillion-dollar impacts down the road on things like operational efficiency, time to market and LIMS return on investment (ROI).[Read More]
October 30, 2019 - Cultivating a Strong Corporate Culture to Attract and Retain Talent
The booming economy and record low unemployment in the United States has many companies struggling to attract needed talent amid tight labor pools. In addition to this talent shortage, the digital age has engendered greater workforce mobility. Using websites like Glassdoor, LinkedIn, Facebook, and others, employees can now easily become aware of other opportunities and find a job that better aligns with their values, goals and interests. A new survey from CareerBuilder revealed that, while 50% of workers feel like they have a long-term career at their current company, the other half feel like they just have jobs. A surprising 32% of survey respondents plan to change their jobs this year. A recent Labor Department report confirmed that these employees are in fact following through on their intentions – the number of employees voluntarily leaving their jobs is at the highest rate it’s been since 2001. To keep pace with technological advances and remain competitive, companies require an experienced workforce with institutional knowledge to maximize productivity and operational efficiency. Given these trends, employee engagement and retention have emerged as top issues for business leaders.[Read More]
October 30, 2019 - Live Webinar: Preparing for an ISO 17025 Audit: What to expect from a LIMS?
October 30, 2019 - Matrix Gemini LIMS Improves Water Testing Laboratory Efficiency
October 23, 2019 - How the UK Biobank is Revolutionizing Precision Medicine
In the last decade, there has been a paradigm shift in the development of gene sequencing diagnostics. This revolution has occurred mainly due to the development of ultra-high throughput next-generation sequencing (NGS) technology that allows a human genome to be sequenced in just a few days. Combined with clinical data, readily accessible genomic data is also accelerating the development of personalized, targeted treatments in a medical model known as Precision Medicine. The UK Biobank Project is on the forefront of this initiative. In order to develop the genetic diagnostics and personalized treatments characteristic of Precision Medicine, scientists must sift through and effectively analyze immense data sets. This necessity has led to the rapid growth of a new engineering field known as bioinformatics – an interdisciplinary field of scientific research that utilizes biology, computer science, data engineering, mathematics and statistics to increase our understanding of biological processes. Bioinformatics has played a major supportive role in the emergence and continued development of precision medicine. Bioinformatics scientists need access to the health and genetics data of large cohorts so that the influence of genetics on disease states can be sussed out and incorporated into tailored treatments. In order to facilitate access to the large amounts of biological and health data that bioinformatics scientists need, many nations have launched biobank projects, including the United States, United Kingdom, China, Austria, Qatar, Estonia, Japan, Canada and Finland. The United Kingdom’s Biobank (UKB) project recently released a vast collection of genetic data to health researchers around the world, offering an unparalleled resource to enhance our understanding of human biology and aid in the advancement of precision medicine. In this blog, we will discuss the types of data made available by the UK Biobank project, along with the details on how scientists can access this important data.[Read More]
October 16, 2019 - Back from the Europe Biobank Week 2019
October 16, 2019 - Target Analysis S.A. is the new QLIMS distributor in Greece
We are pleased to announce that renowned solution provider of the scientific sector, Target Analysis, will be adding QLIMS to their product portfolio and be our new sales distributor in Greece.
Adding QLIMS to their portfolio fits in with their vision to provide quality services that will highlight Target Analysis SA as a Total Solution Provider for the supply and after sales support of scientific equipment and software.
Their product range includes: pre-owned systems, analytical instruments, consumables & spare parts, laboratory equipment, software, solvents & chemicals, by a wide network of internationally recognized manufacturers.
In conjunction with ELBIS's establishment of the QLIMS support centre in Thessaloniki, this partnership now puts Greek laboratories in the unique position of having local access to:
- a highly trained sales team - Target Analysis
- a quality LIMS solution available in Greek - QLIMS
- local support and technical service – ELBIS
October 16, 2019 - Strategies for Surviving an FDA Audit
As part of its mission to ensure public safety, the FDA inspects manufacturers or processors of FDA-regulated products to verify that they comply with relevant regulations. The FDA also inspects facilities that conduct clinical trials with humans and laboratories that conduct studies with animals or microorganisms when these studies are used to apply for FDA approval of a medical product. A typical inspection will last for 2-3 days. In the United States, the FDA is not required to provide advance notice of an inspection. In facilities where violations were noted during a previous inspection, the FDA will likely provide no advance notice. If your last inspection was without violation or if this is a pre-approval visit, however, you will likely be given notice of an impending inspection. There are few events that engender as much anxiety for company stakeholders as an FDA audit. Are you prepared for when the FDA shows up at your front door? Do your employees know how to interact with FDA inspectors when they are on site? Do you have Standard Operating Procedures (SOPs) in place for handling an FDA audit? Surviving an FDA audit can be significantly less daunting if you know what to expect and have a strategy in place to ensure the best possible outcome. In this blog, we will provide best practice guidelines to help you prepare for an FDA inspection, as well as understand how to best interact with the inspector – both while they are on site and post-inspection.[Read More]
October 9, 2019 - New QLIMS European Support Centre
OnQ Software and ELBIS are proud to announce the opening of the new QLIMS European support centre and LIMS centre of excellence. The centre will be based in Thessaloniki, Greece at the offices of leading Greek electrical engineering and IoT development company, ELBIS. We are happy to leverage ELBIS skills and reputation for providing excellent customer support to ensure QLIMS customers have the best experience possible. The centre of excellence will allow for:- Provision of support and technical services to European QLIMS customers
- Showcase of next generation technologies and integrations relating to LIMS


