PDF-Biotherapeutic Medicines
Author : gabriella | Published Date : 2022-08-16
What is so special about how they are made How to di31erentiate them A medicine which has been licensed by the national regulatory authorities on the basis of a
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Biotherapeutic Medicines: Transcript
What is so special about how they are made How to di31erentiate them A medicine which has been licensed by the national regulatory authorities on the basis of a full registration dossier ie th. Programme. General overview and . update. Dr Milan . Smid. WHO Prequalification of Medicines Programme. Amman, June 2013. UN Prequalification . Programme. . for Priority Essential Medicines. Action plan of UN from 2001 for expanding access to selected priority medicines . Cochin University of Science & Technology . Sakthivel. . Selvaraj. Public Health Foundation of India . New . Delhi . (shakti@phfi.org). Access to Medicines in India . Key Barriers to . Access to Medicines . –. lessons from HIV. EPIP, 5 September 2017, Bordeaux. . Ellen ‘t Hoen, LLM. University Medical Centre Groningen, Global Health Unit. @. ellenthoen. www.medicineslawandpolicy.org. Brief history. Programme. General overview and . update. Dr Milan . Smid. WHO Prequalification of Medicines Programme. Amman, June 2013. UN Prequalification . Programme. . for Priority Essential Medicines. Action plan of UN from 2001 for expanding access to selected priority medicines . 201. 7 . China/EU Pharmaceutical Industry Forum. May. 17, 2017 . Shanghai, . China. . By . Mart Levo. REKS Estonia. Mart.Levo. @. reks.ee. Safety Features – Impact on Stakeholders. EMVO, EMVS and NMVOs. Dr Ivana Knezevic TSN/EMP/HIS. WHO, Geneva, 5. th. November 2014. . EMP Technical Briefing Seminar. Outline. . Norms and standards for biologicals in the context of WHO. Strategic . drivers and issues. Presented by . Deirdre Dimancesco. Department of Essential Medicines and . H. ealth Products, WHO. at the . Technical Briefing Seminar. 15 April, 2013 . MeTA. aim. MeTA aims at improving access to quality medicines by increasing transparency of the pharmaceutical sector through collection of reliable data, valid analysis, and then disclosure for advocacy and policy dialogue among stakeholders.. ECBS: Vaccines and Biotherapeutic products Dr Ivana Knezevic TSN/EMP/HIS WHO, Geneva, 5 th November 2014 EMP Technical Briefing Seminar Outline Norms and standards for biologicals in the context of WHO kD 0A4S2UA 34A43TIKA CONSUMPTION2016x0080i tAT AH9bTowASTATE AGENCY OF MEDICINES2017Autors/ Authorx0080u valsts aentraSagatavoja/ Prepared by ASeilisA x0080aeEDailteIdevjs/ Publisherx0080u valsts aent Once . the protection of the product . expires for . example, patents or regulatory protection such as data . exclusivity, . the company no longer has exclusive rights to sell the medicine. . Other . Medicines Manufacturing in the UK 2017. Welcome by Andy Evans. Chair, MMIP. Site Lead, AZ Macclesfield. Morning Agenda. 10:00. Introduction. Steve. Thompson ABPI. Steve Bates BIA. Sue Dunkerton KTN. 2018. Objectives. Prescribing & Zero tolerance. National Alerts . Medicines Reconciliation. Policies. Pharmacy Services . . . “The General Medical Council (GMC) states that . all. doctors must keep . Basic enquiry answering. September . 2016. Session aims. Increase awareness of the Medicines Information (MI) services. UK. Wales. Increase awareness of the questions to ask an enquirer. Have practical experience using some resources which will be... Dr. Richard Torbett. Chief Economist, EFPIA. China/ EU Pharmaceutical Industry Forum. Shanghai, . 16 May 2015. Policy debate on health in recent years has been dominated by cost containment. Health & Growth.
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