- Your Challenges
- News & Events
- Knowledge Center
- About Us
We are a total solutions partner for your entire sample and product lifecycle. No matter your size or industry, our Professional Services team will work with you to design and configure the STARLIMS solution to fit your organization’s unique needs. From implementation to training, you’ll work with industry experts throughout who will help streamline your lab operations for operational excellence.
More than 300 Abbott Informatics professionals around the world are dedicated to supporting our customers quickly and effectively. View all of our local office locations.
Designed by subject matter experts, our solution was built for your lab’s unique environment. When you're ready to scale lab operations, STARLIMS will scale too. Intuitive configuration tools enable you to customize lab workflows and fine-tune your solution as your organization grows.
Our team members have an average of 30+ years of prior experience and operational expertise in various domains, helping your lab meet distinct, industry-specific standards and software regulations.
We adhere to the following standards and memberships: GAMP5, ISO 9001, PMBOK 2000, HL7, ITIL v3, American Society for Clinical Pathology, Project Management Institute, ASTM International, American Society for Quality, and the International Society for Pharmaceutical Engineering.
Our thorough and proven methodology helps ensure that your STARLIMS software solution implementation happens on time and on budget—with no surprises. Throughout the process, our Professional Services teams will act as a true extension of your lab to ensure a smooth implementation and long-term success with the STARLIMS solution.
We get to know your business from the inside out. First, we’ll learn about your goals and business needs. A review of your lab workflow and instrument integrations will help us identify areas of improvement. And finally, alongside your IT infrastructure team and other lab stakeholders, we’ll work together to define software requirements and plan for a successful data migration.
Using the project plan as a roadmap, our software engineers configure and implement the STARLIMS solution, collaborating closely with your team throughout the process. Our development goes through comprehensive quality assurance testing to ensure that your solution meets the highest standards. Transparency and effective communication is key during this time, so we’ll constantly share the project’s progress, preview features, and make adjustments as needed. Hands-on training will ensure that your team fully understands how to operate and maintain the system for future enhancements.
Once the solution is installed and tested, we will assist you through validation processes for industry standards or regulatory bodies before deployment. We will be on-site at your facility during deployment to ensure that the rollout of your solution happens smoothly and efficiently.
After your solution has deployed, we’ll still be here to help answer your day-to-day questions, provide ongoing technical support, and plan for your future needs. We offer multiple in-person training sessions in four of our global offices, in addition to online training. Our comprehensive training offerings will ensure that your team is armed with the skills needed to get the most out of your LIMS solution.
Sign up to receive the latest informatics resources, including webinars, case studies, and more.
Links which take you out of Abbott worldwide websites are not under the control of Abbott, and Abbott is not responsible for the contents of any such site or any further links from such site. Abbott is providing these links to you only as a convenience, and the inclusion of any link does not imply endorsement of the linked site by Abbott. The website that you have requested also may not be optimised for your screen size.
Please be aware that the website you have requested is intended for the residents of a particular country or countries, as noted on that site. As a result, the site may contain information on pharmaceuticals, medical devices and other products or uses of those products that are not approved in other countries or regions.