Dr. Sharon Hertz is a trained neurologist who is currently...

Dr. Sharon Hertz is a trained neurologist who is currently a supervisory medical officer with the Food and Drug Administration. She works in the Division of Anesthesia, Analgesia, and Addition Products (DAAAP) in the Center for Drug Evaluation and Research. By having background in clinical practice, as well as nearly 15 years with the FDA, she as a unique perspective on public health that includes both individual treatment as well as broad public policies. In her position in DAAAP, Dr. Hertz acts as a deputy director of the division and a direct supervisor for ten physicians and oversees the work of chemists, animal pharmacologists and toxicologists, clinical pharmacologists, physicians, and statisticians. The division as a whole provides†¦show more content†¦Dr. Hertz is often called upon to give presentations within her agency or to outside groups including non-profits and the media. Over the long term, she helps to set policy requirements for drug approvals, safety monito ring and safety programs for analgesic products. During the government shutdown in October, it became clear that being a federal employee is not always easy and it is a position that can be vastly different from being a private employee. Dr. Hertz echoed this sentiment by saying that the current budget sequestration and government shutdown indicate the largest difficulties that federal workers face. In her mind, Dr. Hertz believes that federal employees have recently been used as political pawns that have been used by a heavily divided Congress who is often unable of collaboration. She also believes that this use may lead to long-term implication on the federal workforce. Seeing federal workers and the federal budget used in an unfair manner is not only demoralizing to current workers, but has also seriously affected recruitment and retention efforts for qualified candidates who worry about the long-term viability of a career in the federal government. Dr. Hertz indicated that Congr ess needs to stop violating federal workers in this way if they desire to continue to have a force of intelligent, hard-working federal employees to support the actions of our nation. Like thousands of others, Dr. HertzShow MoreRelatedFda Policies5132 Words   |  21 PagesU.S. Food and Drug Administration (FDA) drug review bears a structural similarity to many decisions made by other regulatory agencies: high uncertainty, low reversibility, avoidance of observable error, and high political stakes that induce lobbying by interested parties. This project explores the policy lessons to be learned from viewing FDA drug review as a politically shaped exercise in information processing. I argue that the incentives facing regulators induce limits on the degree to which drugRead MoreEssay On The FDA1104 Words   |  5 Pagesallowed access to potentially life saving medications, if they have not been approved by the FDA. Now, in theory, this should be a fine system by which the FDA, a fed eral government organization dedicated to medication research and safety, receives research on new experimental drugs and either approves, requires more research, or denies it. This is the case, but with one drastic problem: restrictions and time. The FDA is notoriously known for the numerous amount of years it takes them to approve a medicationRead MoreFDA Essay1067 Words   |  5 PagesThe U.S. Food and Drug Administration (FDA) is the governmental division that protects the public’s health by guaranteeing food, drugs, and medical devices are safe and effective. It assures that dietary supplements and cosmetics are well labeled, regulates tobacco, protects the users from electronic product radiation, among others. Deputy Director of The Division of Industry and Consumer (DICE), Bill Sutton explains how the FDA is set and works. FDA was given the duty of regulating all medicalRead MoreEssay On The FDA763 Words   |  4 PagesThe FDA is and agency that falls into the Department of Health and Human Services under the Executive Branch, probably the most interesting agency in my eyes because of its importance in the nation and how a mistake from them or maybe a wrong move can be lethal. This very important agency can actually be traced back to the 1800s but bills were placed after it earlier agencies to become what it is today after protests and cries of those living in the nation around the early 1900s. (Office of theRead MoreHistory of Fda2718 Words   |  11 PagesHistory of the FDA From a staff of one to over 9,000, the Food and Drug Administration has seen great changes since it was first created in 1862. Stemming from a single chemist in the U.S. Department of agriculture, the FDA now encompasses most food products, both human and animal drugs, cosmetics and animal feed. The FDA received it start under a different name. First called the Division of Chemistry, which played a small part in everyday life, then in July of 1901, the name was again changedRead More FDA Evaluation of Medication Essay1127 Words   |  5 Pages FDA Evaluation of Medication Introduction The main center within the FDA for the evaluation of medication is known as the Center for Drug Evaluation and Research. The center evaluates all drugs before they are sold. It currently evaluates more than 10,000 drugs that are on the market to ensure that highest standards of those drugs. They also monitor media broadcasts to make sure that messages portrayed are truthful to consumers. Lastly, they provide health care professionals as well as consumer’sRead MoreDisposal Of Unused Medications ( Fda ) Essay969 Words   |  4 Pagesto prevent drug diversion and protect our environment the FDA scheduled take –back days and proposed safe and effective strategies of drug disposal. Response/Literature review For many years, limited options and lack of proper education on medication disposal have contributed to increasing rates of environmental pollution and drug abuse. In order to prevent accidental or intentional misuse of the drugs Food and Drug Administration (FDA) recommends that consumers discard their unused medicationRead MoreRegulations Of The Fda On Cosmetics Essay1743 Words   |  7 Pages Limited regulations of The FDA on cosmetics Frequently, consumers like you and I buy items everyday not knowing chemicals or harsh byproducts that they are made with. We trust that cosmetic products we buy everyday will be safe, but there are ingredients in our daily products that could or has caused some health or skin conditions. In 1820, the U.S gathered physicians to create, The FDA and regulations on drugs in the United States. The general purpose of The Food and Drug Act was to have aRead MoreThe And Drug Administration ( Fda )1460 Words   |  6 PagesBackground and Introduction: Clinical trials evaluating the use of Yttrium-90 (Y-90) transarterial radioembolization for hepatic tumors date back to the 1960s. The U.S. Food and Drug Administration (FDA) approved the use of TheraSphere ® (BTG, Ontario, Canada) particles for hepatocellular carcinoma (HCC) via humanitarian device exemption (HDE) in 1999 and SIR-Spheres ® (SIRTex Technology Pty, Lane Cove, Australia) particles for colorectal cancer metastases in 2002. Since then†¦.[talk more about recentRead MoreFda Research Paper2360 Words   |  10 PagesFDA Drug Approval Process Tricia Garbuzovas COM/172 October 5, 2011 Cassandra Baker FDA Drug Approval Process Americans must wait up to 19 years after a discovered treatment before they can participate in benefits of a new medication (Philipson Sun, 2008). The regulatory process drug manufacturers need to endure before releasing potentially life-saving medication is an extremely expensive, time-consuming process. The Center for Drug Evaluation and Research (CDER) is the main department