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We have organised the Zenosis library into learning pathways based on job roles within Regulatory Affairs and Clinical departments. This screen (left) illustrates how Zenosis course modules link together to address specific needs of learners, including those new to the Pharmaceutical and Biotechnology industry. Click the image for a larger interactive view (opens in new window).

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An Introduction to Good Manufacturing Practice (GMP) for Drug Products

£ 100.00

GMP is that part of Quality Assurance which ensures that pharmaceutical products are consistently manufactured to the quality standards appropriate to their intended use and as required by a marketing authorisation or product specification. Manufacturers' compliance with GMP legislation is a requirement of approval of regulatory submissions.

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An Introduction to Drug Safety and Pharmacovigilance

£ 100.00

Drug safety monitoring and risk management are vitally important for medicinal product developers, licence holders and clinical investigators. . .

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Pharmacokinetics and Pharmacodynamics in Drug Registration

£ 100.00

Pharmacokinetic and pharmacodynamic (PK/PD) studies play a vital role in drug development. Regulatory authorities are placing greater emphasis on the role of PK/PD in drug registration. This module enables the learner to understand the role of PK/PD data in establishing the safety profile of a new or generic product.

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An Introduction to Good Manufacturing Practice (GMP) for Drug Products

An Introduction to Drug Safety and Pharmacovigilance

Pharmacokinetics and Pharmacodynamics in Drug Registration