Market opportunities lie in enhancing risk-based V&V planning, focusing on DQ, IQ, OQ, and PQs to address cGMP deficiencies and regulatory expectations. By aligning with FDA, ICH, and ISO standards, ...

VP and CISO for Mandiant, helping guide the company's product and solutions strategy and host of the Cyber Security Effectiveness Podcast. Understanding the effectiveness of your company's security ...

In September 2025, HPQ received strong third-party validation of its silicon-based anode materials initiative through the ...

Developing a medical device is a lengthy process. Prior to commercial distribution, FDA requires that the manufacturing process for the product be validated. Process validation is defined as the ...

COLORADO SPRINGS, Colo.--(BUSINESS WIRE)--Eclypses, a leader in end-point data protection, today announced that it received the Federal Information Processing Standard 140-3 (FIPS 140-3) validation ...

Discover how automation is revolutionizing laboratory processes, changes in the regulatory landscape, and how labs can stay ...

Report Provides Key Insight on How and Where ID Validation Is Used Greenway Solutions research also yielded some valuable industry insight on where, how, and when identity validation technology is ...

Process validation is crucial for ensuring the quality of final products and the safety of these processes for manufacturing personnel and consumers in the pharmaceutical, medical device, and ...

Aduro Clean Technologies Inc. achieved third-party validation of its Hydrochemolytic technology (HCT) and its application in circular plastics value chains through a series of pilot-scale ...