How we help with Software Optimization
As the life science product development ecosystem continues to evolve at a rapid pace, the key to achieving success is aligning a company’s vision with strategic technology implementation. Halloran’s software optimization and implementation services are designed to meet our client’s needs, whether it’s providing a tailored technology roadmap, vision futureproofing, enabling better data-driven decisions, or anything in between.
The technology ecosystem in clinical development is expanding exponentially, and with this development, there is more operational complexity. In response, regulatory agencies have outlined many regulations and guidelines for the use of electronic systems and signatures, and life science companies must establish quality baselines for how software is developed and maintained. Halloran consultants leverage their expertise to help companies define business processes related to software development and system administration to ensure companies select and implement software in a controlled and compliant manner.
Halloran’s CORE East, a three-day intensive retreat for clinical operations executives and life science leaders, is the epicenter of a movement aiming to disrupt the traditional landscape of clinical research. The best and brightest came together and sought to revolutionize the drug development process and its impact on healthcare. A few sessions emphasized embracing the […]
The use of Veeva systems, a suite of clinical trial solutions, continues to grow. Veeva’s products offer robust functionality, a clean user interface, and excellent reporting capabilities, making their products an industry favorite for small and large life science companies. However, companies must be prepared for all the changes that come with implementing a new […]
The European (EU) Medical Device Regulation (MDR), adopted in 2017, was a sizeable update to medical device regulations. The EU MDR is a new set of regulations governing the production and distribution of medical devices in Europe, and more specifically, designed to modernize the EU regulatory system to better address the current needs of the […]