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Viewing ALL listings in Verification
Stratos Product Development LLC
Product Development Experts – Medical Devices and Consumer Electronics Since 1987, Stratos has been the trusted resource for science and technology innovators. Our team has decades of experience spanning drug delivery systems, minimally-invasive surgical devices, patient monitor...
HS Design Inc.
...Manufacturing Transfer. A superior network of QMS relevant partners offers a turn-key experience from design though full production, including design verification and validation, molding, packaging, and contract manufacturing. User-Centered Process and Core Capabiltiies For...
Promenade Software, Inc.
...or you can choose the provider of your choice. Our RESTful API simplifies access from PC, device, or mobile. Testing Services Verification and Validation are key aspects of any medical device development and Promenade Software can assist. We help clients re...
Intertech Engineering Assoc., Inc.
Intertech Engineering Associates Inc. specializes in disciplines centered on medical device software. The company supports its clients through all phases of product development. Disciplines include software development and validation (including 820.70 and Part 11 validations), requ...
Symbology, established in 1980, is a specialty manufacturer of sequentially numbered barcode labels for industry-specific use including medical device and laboratory categories. An ISO 9001:2008 certified company; they also offer a complete line of inspection / verification equipme...
Since 1994 In-Phase Technologies has been supplying our customers with Automatic Test Solutions for their manufacturing facilities. Our test systems measure, Digital, Analog, RF and Microwave components. We have the experience working with FDA, UL and CE requirements.
Sterling Medical Devices
Sterling Medical Devices is an ISO 13485-registered medical device organization offering software/hardware development and validation services. The firm has worked on more than 150 medical systems, including Class I, II, and III devices that resulted in successful FDA 510(k)s, PMAs, and CE submissions.
...time on troubleshooting or waiting for resolution from the broader open source community. SUSE also has experience helping partners reduce their verification cycle time, thus allowing new products to come to market more quickly. Some subscription agreements even include a dedicate...