All Posts

Effective January 1, 2026, California SB 513 expanded employer obligations for training records. If employers maintain training documentation, those records must now include specific details—such as training date, duration, competencies covered, and certifications—and be retained for at least three years after employee separation. These records are now treated as personnel records and must be produced upon request.

ISO 13485 is the global quality management standard for medical devices. This guide explains the core requirements—QMS documentation, risk management, internal audits, and corrective actions—and offers practical steps to assess gaps, build audit readiness, and achieve certification with confidence.

An ISO 9001 certification can help you establish a robust and reliable quality management system for your business. This empowers you to be able to consistently provide products and services that meet customer and applicable legal and regulatory requirements. By putting a system in place, you are able to facilitate opportunities to enhance customer satisfaction and continually improve the customer experience.