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Live Webinars Page
|Informed Consent||Tue, 09/10/2019 - 10:00am||
Clinical research studies conducted in the US are regulated by the Food and Drug Administration (FDA) and by the Federal Food, Drug, and Cosmetic Act, as amended (secs. 201-902, 52 Stat. 1040 et seq. as amended (21 U.S.C. 321-392)). Throughout the research process, there are legal and ethical implications that researchers and doctors, clinical trial sponsors, and drug development companies must be aware of to successfully bring drugs and medical devices to the consumer market.
|Medical Malpractice Litigation - The Paralegal's Role||Wed, 09/25/2019 - 11:00am||
Medical malpractice litigation combines all the demands of complex litigation with a wide range of challenging medical issues. This webinar will provide an overview of medical malpractice litigation from pre-suit through trial, while focusing on the paralegal’s role as part of the medical malpractice team. Attendees will learn strategies for paralegals at each stage of a medical malpractice case, including medical literature research; records collection and analysis; expert research and retention; trial preparation; and trial support.