Efficiently ensuring software quality is a critical step in a life science organization’s journey to stay competitive. Test automation is a strong enabler in achieving this goal, as it can improve testing efficiency and coverage, assure software quality, and reduce costs.
Test automation is a key element of the concept digital transformation. Its implementation is often a part of an organization’s strategies to increase the digitization of processes and systems. In fact, this is considered a core principle in Computer Software Assurance for Production and Quality System Software, the FDA’s draft guidance intended to drive a risk-based approach to validating computerized systems that are part of the production of medical devices or an organization’s quality system.
Before test automation was introduced in life sciences, nearly all testing was performed manually – which often meant extended project timelines, an inability to extensively test all relevant scenarios, inconsistent results (especially with data verification) and higher costs. Since the early 2000s, test automation has been a central part of how organizations perform test-execution activities. Below, we cover the top reasons for adopting test automation within your organization.
Test automation is more than just a tool – it’s an investment that transforms an organization’s testing framework. It empowers organizations to meet the demands of modern software development and implementation with quality assurance seamlessly integrated throughout the entire process.
Adopting test automation is an essential step in the digital transformation journey for leaders in life sciences. Please reach out to our IT quality & compliance team to discuss your unique digital path and learn more about our best practice-based insights.
For over a decade, Suneetha Bellamkonda has delivered global solutions for Enterprise Quality Management Systems, designing TrackWise and industry best practices in the U.S., Europe, and Asia-Pacific. As a validation manager, Suneetha offers validation services of TrackWise and TrackWise Digital systems from multiple enterprises and global customers. She is instrumental in validating global systems for Fortune 500 organizations in both pharmaceutical and life sciences companies.
With nearly a decade of experience validating global, regulated systems, Mike Hulbert is the client engagement manager in Sikich’s IT Quality & Compliance practice. A former CSV consultant, he aligns client needs with ITQ&C services to implement risk-based solutions. Mike has consulted for multiple Fortune 500 life sciences companies and is passionate about client success.
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