Biopharmaceutical research and development is knowledge and skill intensive and, further, global regulations require that sponsors employ individuals qualified by education, training, and experience. Each organization should consider which courses can be offered effectively with internal resources at a minimum opportunity cost and, conversely, which courses should be offered with external resources. Albemarle Scientific
Consulting members teach in our focus areas of GXP Compliance including 21 CFR Part 11, Patient-reported Outcomes (PRO endpoints), Statistical Topics in Clinical Research for Non-Statisticians, and Virtual Drug Development. A common outline for course development begins with a review of the general topic and an assessment of existing teaching resources. With agreement by the client organization, the syllabus, length, and difficulty level are set. Next, course development advances to a client acceptance stage followed by delivery to the target learners. To request a proposal for training customized to a particular literature
or a specific challenge faced by your organization, navigate to the
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