Verista Sets New Standard for Commissioning, Qualification, and Validation Services in Medical Device Manufacturing

Verista, a leading provider of automation, compliance, and quality solutions for the medical device industry, is redefining service excellence for medical device manufacturers by providing comprehensive expertise in commissioning, qualification, and validation that ensures both speed and uncompromising quality. With digital validation strategies and risk-based, phase-appropriate methodologies, Verista helps manufacturers bring innovative devices to market up to 40 percent faster.

As the medical device industry faces increasing regulatory scrutiny and accelerated market expectations, Verista empowers clients to meet these challenges with end-to-end support throughout the full product lifecycle. The company’s specialization extends from product and equipment design to process automation, rigorous hardware and software testing, and robust validation protocols. This service-focused approach ensures every device, whether it’s a glucose monitor, heart rate sensor, or complex combination product, is thoroughly prepared to meet stringent regulatory requirements, mitigating risk and streamlining approval timelines.

Verista’s medical device services are distinguished by teams of highly experienced engineers and scientific experts who collaborate closely with clients to ensure testing and validation are both complete and timely. The firm’s proprietary expertise ensures that client projects benefit from real-time project visibility, compliance with the latest regulations, and the flexibility to quickly adapt to new challenges. Additionally, Verista’s digital validation platforms and leading partnerships deliver secure, fully documented workflows, offering clients unmatched confidence and regulatory peace of mind.

By partnering with Verista, medical device companies gain the security of knowing that every facet of device development, testing, and launch is guided by best-in-class engineering, proven digital tools, and an unwavering focus on quality. This comprehensive, service-led model guarantees that medical innovations not only reach market efficiently, but also uphold the highest standards for patient safety and product reliability.

About Verista 

Verista is a leading provider of quality and compliance solutions for the pharmaceutical, biotechnology, gene therapy, and medical device industries. Headquartered in Fishers, Indiana,  Verista specializes in services such as computer systems validation, commissioning and qualification (CQV), manufacturing and packaging automation, machine vision, and regulatory compliance. Leveraging innovative technologies and over 500 industry experts, Verista helps clients ensure data integrity, meet stringent regulatory requirements, optimize operations, and accelerate time-to-market for life-saving products. With a focus on digital transformation and operational excellence across the product lifecycle, Verista provides consistent, safe, and high-quality results every time.