Course Description

Pharmaceutical law and administration is a key foundation knowledge requirement for all Qualified Persons (QPs). This is clearly spelled out in the relevant article of European Directives 2001/82/EC and 2001/83/EC and in the current Qualified Person Study Guide. The QP must ensure that the relevant laws are being complied with. Thus, a thorough understanding of the laws and legal processes, within Europe and beyond, is essential. This is equally true for other pharmaceutical technical managers. This extremely popular QP training module is designed to ensure that, in an increasingly changing world, you have a deep and detailed understanding of… Why we have medicines laws and what they seek to achieve - The laws and legislative processes within the EU which impact on medicinal products, and hence the role of the QP - The UK medicines legislative framework - US and other international pharmaceutical legislation - Other relevant laws

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