PPT-Non-sterile compounding PTCE Practice Questions
Author : ellena-manuel | Published Date : 2018-11-22
Question 1 Which of the following establishes standards of quality strength purity packaging and labeling for compounded medications USPNF FDA ASHP DEA Question
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Non-sterile compounding PTCE Practice Questions: Transcript
Question 1 Which of the following establishes standards of quality strength purity packaging and labeling for compounded medications USPNF FDA ASHP DEA Question 1 Which of the following establishes standards of quality strength purity packaging and labeling for compounded medications. Background on STERILE PREPARATION COMPOUNDING Safety General information Stakeholder Collaboration Goals for the summit Disclosure Proposed USP Chapter <800>. on Hazardous Drugs. Bill Peters. NuAire, Inc.. Safe Compounding Act of 2013. Gives FDA authority for compounding. Over 80 483s and warning letters issued to what will be considered FDA outsourcing facilities. parenterals. , Total Parenteral. Nutrition and Intravenous additives.. Injections . These are the preparations which are given other than oral routes. . Injections are sterile, pyrogen-free preparations intended to be administered . Frederick M. Frankhauser, JD, MBA. Adjunct Assistant Professor. MCPHS University. Objectives. 1. Provide an brief overview in the recent changes in pharmacy compounding regulations. 2. Describe the Drug Quality and Security Act and its impact on pharmacy. USP/NF 797 requires that air sampling for high risk level areas be performed at least:. Daily. Weekly. Monthly. Annually. weekly. How often must work surfaces in the ISO Class 7 and 8 area buffer/clean rooms be cleaned?. CHAPTER . 9. CHAPTER OUTLINE. Compounding Sterile Formulations. Special Considerations. Regulatory Oversight. LVP Solutions. SVP Solutions. Special Solutions. Administration Devices. Laminar Flow Hoods. Stephanie Montoya, CPhT. Coryann. . Senteno. , CPhT. Objectives:. At the completion of this application-based presentation, the Pharmacist participant will be able to: . 1) Accurately calculate the correct amounts of ingredients for a compounded product. . Danielle Fagnan, . pharmacist. ,M. Sc.. . Director. of . professional. services. Ordre des pharmaciens du Québec. NAPRA March 13. ,. 2014. Standards for pharmacy compounded sterile preparations. Jessica Tagerman, . PharmD. , . RPh. Compounding is like cooking!. “What are we making?”. Medication- . “What are we making?”. i.e. “medication preparations”. “What are we making?”. Dosage Forms. What is the name of the . document with approved agents . to be used in an institution or reimbursable by an insurance plan?. a. database. b. policy. c. legend. d. formulary. formulary. When checking in an order from the wholesaler, against which of the following documents should the order be checked?. Question 1. Which of the following medications requires that a patient product insert be provided to the patient?. Atenolol. Erythromycin. Medroxyprogesterone. Naproxen. Question 1. Which of the following medications requires that a patient product insert be provided to the patient?. CompoundingSterile Preparations detailed in Pharmaceutical Compoundingibe practices to provide a reasonable assurance of maintaining patient safety associated with the administration of 34 Committee s Pharmacy . Technician Education. ASHP Section Advisory Group on Advancing Pharmacy Practice with Technicians 2018-2019. Table of Contents . Didactic overview of types of hazardous drugs (HD) and their risks. [READ] PTCB Exam Prep 2022-2023: Updated Study Guide + 540 Test Questions and Detailed Answer Explanations for the Pharmacy Technician Certification Exam 6 Full-Length Practice PTCE Tests
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