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Medical Devices, Pharmaceuticals

EU Directives and Inspection Readiness

About the Course

The EU has strict requirements for the manufacture and supply of medicinal products, which are defined in EU directives and Good Manufacturing Practices (GMP) guides. To confirm that these requirements are being complied with, manufacturers and suppliers are regularly inspected. If significant deficiencies are identified during inspections, the company may face sanctions and could even be barred from supplying products. Upon completion of this eLearning course, you will be able to identify the regulatory background regarding EU inspections, the expectations of inspectors, and how to prepare for inspections.