PPT-US Regulatory Pathway For Biosimilars

Practical LegalRegulatory Considerations Arising In The Course Of The Pathways Implementation John M Engel Esq Managing Partner Engel amp Novitt l lp The Law Firm That Knows Its Science. Presented by . the Alliance for Safe Bioloigic . Medicines & the Global Colon Cancer Association. . . . . Andrew Spiegel, Esquire. . . andrew.spiegel@globalcca.org. THANK YOU! . Knowledge Connect Slide Resource. This slide deck has been designed to be used as a central resource from which pertinent slides can be extracted as needed . and is not intended for use in its entirety. Introduction/Overview . PLANETRA Extension Study: . ACR50 Response Rate. Etanercept vs SB4 (Etanercept Biosimilar): ACR20 Response Rates. Typical Study Design for Biosimilar Switching Studies in Rheumatology. OMICS Group Biosimilars 2015 Birmingham, UK. 10-11 Aug 2015. Hazel Gorham . GorhamHazel@prahs.com. Topics. What is a Biosimilar and Why?. Demonstrating Similarity . Quality attributes. Non-clinical animal. Animation: What Are Biologics?. Production of Biologics. Sources of Variation in Biologics. Variability Is a Natural and Expected Property of All Biologics. Glycosylation Affects Protein Properties. Most Biologics Have Undergone Manufacturing Changes. interchangeability,extrapolation. and safety. Dr . Valderílio. . Feijó. . Azevedo. , MD, PhD. Universidade. Federal do Paraná. Edumed. Biotech. . Adjunct professor of rheumatology at the Federal University of Paraná, Brazil . . Agenda. Key Regulatory Exclusivities for Biologics. Additional Regulatory Exclusivities. Patent Strategy for Biologics. Comparison Between the 262(k) Pathway and the ANDA Pathway. Comparison Between the 262(k) Pathway and the ANDA Pathway (continued). Kevin Olson, CEO. Industry Standard Research. KevinO@ISRreports.com. October, 2015. Table of contents. ASBM - US Prescribers and Biosimilars Naming. 2. Page. 3 . Methodology. 12. . Drug Recording Practices. Ms. Leah Goodman. Contents. Key Messages. An Overview - Biological Medicines and their Regulatory Framework. PhAMA Position and Recommendation on Biosimilars . An Overview - Biological Medicines and their Regulatory Framework. By. ANSHUL . SHARMA. Graduate Research Scholar. Deptt. Of Biochemical Engg & Biotechnology,. Indian Institute of Technology, Delhi . Biosimilars. Coined by EMA (European Medicine Agency). Bio-betters. Presented at the . Latin American Biologics/Biosimilars Conference. Sao Paulo, Brazil. September 27, 2016. Harry L. Gewanter, MD, FAAP, FACR . Chairman, Alliance for Safe Biologic Medicines (ASBM). Richard . Dolinar. , MD. Endocrinologist, Chairman of the Alliance for Safe Biologic Medicines. Presented at the . Colorado . Biosimilars. . Educational Forum  . December . 6, . 2012. 2. The differences between Chemical Drugs and Biotech Medicines you . Dr.G.Hima. . Bindu. . MD; PG dip. . diabetology. Asst.Professor. Dept. of Pharmacology. Rajiv Gandhi Institute of Medical Sciences. Ongole. QuestionsCircle the Best AnswerWould you rather take an Englishor Social Science class OR a Mathor Scienceclass Circle your first choiceCircle one columnEnglish orSocial ScienceclassEx History geograp