When it comes to medical device software compliance, verification and validation are closely related, but not equal.
Continue readingThe Bottom Line on Medical Software Validation
What a Device Master Record Is and Why It’s Important
Maintaining a robust DMR will make your manufacturing processes easier and keep you out of hot water with the FDA.
Continue readingUnderstanding Medical Device Validations
Validating medical devices is a critical step that cannot be overlooked in design and manufacturing. The necessity for developing safe healthcare tools.
Continue readingHow Development and Validation Are Changing for the Life Sciences Industry
As COVID-19 continues to spread across the globe, life science companies are doing everything possible to facilitate the manufacture of critical medical supplies and the development of an effective vaccine. Find out how many organizations within the life sciences industry are attempting to expedite every possible aspect of the development and validation processes.
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