PPT-1 AAVPT Veterinary Drug Regulatory Cycle (A to Z)

Author : briana-ranney | Published Date : 2018-09-16

3 March 2011 Mike Murphy DVM JD PhD Veterinary Medical Officer Division of Surveillance Advertising Issues Effectiveness Claims 2 AAVPT Veterinary Drug Regulatory

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1 AAVPT Veterinary Drug Regulatory Cycle (A to Z): Transcript


3 March 2011 Mike Murphy DVM JD PhD Veterinary Medical Officer Division of Surveillance Advertising Issues Effectiveness Claims 2 AAVPT Veterinary Drug Regulatory Cycle A to Z 3 March 2011 . Pain Management – Cats and Dogs. Cory Theberge, PhD UNE College of Pharmacy. MPA Spring Conference CE 2015. Learning Objectives. Identify the physiological characteristics of cats and dogs that affect pain medication absorption, metabolism, and excretion. 3 March 2011 . Mike Murphy DVM, JD, PhD. Veterinary Medical Officer. Division of Surveillance. Advertising Issues, . Effectiveness Claims. 2. AAVPT Veterinary Drug Regulatory Cycle (A to Z). 3 March 2011 . the Pharmaceutical Sector - Current Scenario and Main . Challenges. . Dr. B R JAGASHETTY. . B.Sc. ; . M.Pharm. ; LLB; . Ph.D. Drugs Controller, Karnataka State. 04.10.2013 . Oehlsen. International Policy Analyst. International Programs Team - Office of the Director. Center for Veterinary Medicine. Food and Drug Administration. Lifecycle-Based Approach to Regulating Product Quality an International Perspective. Director . International Programs. Center for Veterinary Medicine. U.S. Food and Drug Administration. Governance of Veterinary Medicinal Products: Need to Leverage Resources. . Authorization of veterinary medicines around the world almost universally requires some sort of premarket clearance or licensing and is based in legislation and regulation. Dr.. P. . Fandamu. Chief Veterinary Research Officer. Presentation outline. Background. Objective of the programme. Materials and Method. Preliminary results. Conclusion. Background. An important aspect food safety (animal derived food) is the control of residues. Presented By: Stephanie . Montoya,. MBA, BS, . CPhT. . . Objectives. Review veterinary pharmacology. List compounding Guidelines (USP 795). Choose appropriate equipment and supplies required to compound veterinary preparations. U.S. . Department of Agriculture. Animal and Plant Health Inspection Service. Veterinary Services. November 2013. Veterinary Services. VS Reorganization Drivers. Continual evolution of the animal agriculture industries. International Programs Team - Office of the Director. Center for Veterinary Medicine. Food and Drug Administration. Lifecycle-Based Approach to Regulating Product Quality an International Perspective. Proactive Approach to Drug Residue Prevention. © 2012 Wisconsin Veterinary Medical Association, Inc. Reproduction prohibited without license from WVMA. Wisconsin Veterinary Medical Association. 1994 - AMDUCA Taskforce. Marlene E. Haffner, MD, MPH. CEO, Haffner Associates, LLC. Orphan Drugs Summit 2012. Thursday, 27. th. September 2012. Current . Pharma. Trends. Slow . pharma. industry growth. Patent expiration. Cory Theberge, . phd. . une. college of Pharmacy. MPA 150. th. Annual Meeting Sunday October 15, 2017. Copyright protected and owned by Cory Theberge. Unauthorized use, access, or reproduction is prohibited. . Investigational New Drug Application (IND); Summary of regulations and guidelines . Introduction of . cGMP's. /principles of validation . Introduction to QA/QC principles . Good Laboratory Practice (GLP) compliance . Director . International Programs. Center for Veterinary Medicine. U.S. Food and Drug Administration. Governance of Veterinary Medicinal Products: Need to Leverage Resources. . Authorization of veterinary medicines around the world almost universally requires some sort of premarket clearance or licensing and is based in legislation and regulation.

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