GlobalCompliancePanel

This presentation will go over the steps required for your recruiting process to be successful.

This presentation will provide an overview of the rules and assumptions behind the calibration of analytical instruments.

Food, Drug, and Cosmetic Act history basics will be covered as will implementing FDA regulations relevant to the Food, Dietary Supplement and OTC Drug industries that have followed.

Prior to introduction of a new device, or even a modified design for an existing device, a systematic process must be followed.

This course provides regulatory/quality professionals, manufacturing engineers, and process development engineers with the knowledge and skills needed to comply with the process validation requirements of the FDA's Quality System Regulation,

Virtually all field inspections performed by FDA inspectors are done according to the QSIT.

Supplier qualification and assessment is required in both the QSR regulations and ISO standards.

This interactive webinar begins with an overview of the FDA Inspection process.

This interactive webinar will review the regulatory requirements for an OOS Investigation.

This Interactive webinar will begin with an overview of the GMP/GLP requirements for an Equipment system.