Explore AI governance in MedTech. Learn about regulatory risks, compliance & strategy in our expert-led webinar. Stay ahead in health tech innovation.

Explore how digital transformation is revolutionizing the life sciences industry. Learn how Compliance Group Inc ensures innovation while maintaining regulatory compliance.

Explore how a risk-based validation approach enhances regulatory compliance and reduces costs. See how the combination of CG and Valgenesis delivers smarter and efficient outcomes.

Get insights into the key differences between CSA and regular risk assessment for CSV & why CSA leads to streamlined, risk-based validation.

Organizations in today’s fast-paced, complex business environment turn to strategic consulting to gain a competitive edge, navigate transformation, and drive sustainable growth. While consultants ...

Discover how digitalizing design quality enhances product development. Explore key strategies for effective implementation and adoption of digital tools.

Ensure your FDA inspection readiness with expert guidance! Learn how to navigate audits, maintain compliance, and implement effective CAPA strategies.

Explore the importance of design quality in the MedTech industry and how it drives innovation, compliance, and product success ...

Explore a quality manager's journey through implementing and validating Veeva. Discover practical tips and strategies to overcome common challenges for success.

SOX IT controls in life sciences are vital for ensuring data integrity, patient confidentiality, and regulatory adherence.

ISO 13485:2016 is an international standard for medical device manufacturers and providers of quality management systems. ISO 13485:2016 is not a law or regulation and is voluntary, while FDA 21 CFR ...

Laboratory University contains 3 amazing events at one location! Each event contains a packed agenda with multiple sub-tracks of current regulations, industry trends and key areas of interest. Create ...