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Safety and pharmacovigilance are key activities for ensuring that the right products get to patients at the right time with the right balance of benefits and risks. Optimizing benefit-risk is an important matter not just for regulators, but for all stakeholders, and planning for pharmacovigilance activities and appropriate evidence gathering must be done throughout the medicine life cycle. DIA Learning provides safety and pharmacovigilance professionals with the knowledge needed, from regulations and requirements, to premarket and postmarket monitoring, to stay afloat in the ever-changing world of health care.
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Developed with DIA expertise to meet the unique needs of its stakeholders and members, the Drug Safety eLearning Program provides the knowledge you need, from regulations and requirements through premarket review and postmarket monitoring.
DIA’s Safety and Pharmacovigilance Certificate Program is a comprehensive program based on the DIA Safety and Pharmacovigilance Competency Framework developed with experts working in the field. These competencies outline the functional knowledge and skills needed to work in safety and pharmacovigilance and comply with US and EU regulations. The Certificate Program is designed for individuals new to the field with one to three years of experience, or for those looking to broaden their expertise in this area.