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In this section: For Health Professionals

Learning Activities

CDERLearn in the Center for Drug Evaluation and Research (CDER) offers a variety of learning opportunities for healthcare professionals, industry, consumers, and academia. The goal is to create a body of educational and information modules about human drug regulation and activities. CDERLearn is a way to share FDA expertise in specific subject areas to further instruct the public about the many ways CDER protects and promotes public health. CDERLearn

Sub-Topic Paragraphs

Examining Medical Product Development in the Wake of the Ebola Epidemic -

Examining Ways to Combat Antibiotic Resistance and Foster New Drug Development - 06/14/2017

Researching the Potential Medical Benefits and Risks of Marijuana - 07/12/2016

Reviewing the Rising Price of EpiPens - 09/21/2016

Exploring a Right to Try for Terminally Ill Patients - 09/22/2016

Prioritizing Public Health: The FDA’s Role in the Generic Drug Marketplace - 09/26/2016

Waste and Duplication in the USDA Catfish Inspection Program - 12/07/2016

Prescription Drug User Fee Act Reauthorization (PDUFA VI), Medical Device User Fee Act Reauthorization (MDUFA IV), Generic Drug User Fee Act Reauthorization (GDUFA II), and Biosimilar User Fee Act Reauthorization (BsUFA II) - 03/21/2017

Mar 07

Medtronic Neurosurgery Recalls Duet External Drainage and Monitoring System Catheter Tubing due to a Potential for the Catheter Disconnection from the Patient Line Stopcock Connectors

Medical Devices

Mar 07

Do Not Use Certain Cardinal Health Monoject Luer-Lock and Enteral Syringes – FDA Safety Communication

Mar 07

Cardinal Health Recalls Sterile Monoject Luer-Lock and Enteral Syringes Due to a Change in Manufacturing

Medical Devices

More MedWatch Safety Alerts

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