Clinical Pharmacology Study Conduct Tutorial
The Pharmacology Tutorial is designed to educate clinical research staff conducting clinical trials that have one or more pharmacology objectives.
It provides material on pharmacology concepts, outcomes, designs, sampling, data and measures, and seeks to improve the overall quality of pharmacology-related study procedures. Whether clinical, laboratory, or data entry, the conduct of each team member during the conduct of a protocol is vital to final outcomes. Understanding the basic principals in pharmacology studies improves the quality of clinical trials research.
The Tutorial consists of eight interactive modules on a variety of pharmacology-related topics, from terminology to specimen handling. The full tutorial takes approximately two to three hours to complete, and can be completed over more than one session. After the Tutorial is completed, you are issued a certificate of completion.
Bioanalytical Method Validation
This course provides the learner with information necessary to comprehend, design, perform, analyze, and evaluate bioanalytical method validation. The validation procedures and regulations are applied to chromatographic methods used to quantitate drugs, metabolites, or other small molecules of interest.
LDMS is a laboratory application use for storing and submitting pharmacology data. Training for learning to use LDMS is provided by Frontier Science.
Information about LDMS training is on the LDMS website.
Are you a DAIDS-affiliated laboratory or site interested in additional learning or training opportunities? Contact us.