Devices Compliance Conferences
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This 90-minute presentation will cover the FDA Quality System Requirements for software used in medical devices. The presenter will review FDA guidelines on software verification and validation and discuss methods to verify and validate even complex software.
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This webinar will cover creating of a value-added internal auditing program for compliance to FDA and ISO 13485 internal auditing requirements. It will include how to setup and manage the auditing system, as well as how to conduct an internal audit,and document the results and any non conformities.
By : Redstone Consultants