Risk sharing arrangements for pharmaceuticals: potential considerations and recommendations for European payers.
about
Cost impact of a non-invasive, portable device for patient self-administration of chronic migraine in a UK National Health Service settingPersonalized respiratory medicine: exploring the horizon, addressing the issues. Summary of a BRN-AJRCCM workshop held in Barcelona on June 12, 2014USING CLAIMS DATA FOR EVIDENCE GENERATION IN MANAGED ENTRY AGREEMENTS.Opportunities and challenges in leveraging electronic health record data in oncology.Use of Generics-A Critical Cost Containment Measure for All Healthcare Professionals in Europe?Dabigatran - a continuing exemplar case history demonstrating the need for comprehensive models to optimize the utilization of new drugsComprehensive taxonomy and worldwide trends in pharmaceutical policies in relation to country income status.Market Access Agreements for pharmaceuticals in Europe: diversity of approaches and underlying conceptsThe role of health technology assessment bodies in shaping drug development.Inter-jurisdictional cooperation on pharmaceutical product listing agreements: views from Canadian provincesThe use of risk sharing tools for post adoption surveillance of a non pharmacological technology in routine practice: results after one year.Personalizing health care: feasibility and future implications.Policies to enhance prescribing efficiency in europe: findings and future implications.Patient access schemes in Asia-pacific markets: current experience and future potentialRole of centralized review processes for making reimbursement decisions on new health technologies in Europe.Prospects of risk-sharing agreements for innovative therapies in a context of deficit spending in bulgaria.International variability in the reimbursement of cancer drugs by publically funded drug programsBudgetary impact analysis of buprenorphine-naloxone combination (Suboxone®) in Spain.Discounts and rebates granted to public payers for medicines in European countriesReimbursement of licensed cell and gene therapies across the major European healthcare markets.Dabigatran - a case history demonstrating the need for comprehensive approaches to optimize the use of new drugs.Health economic value of an innovation: delimiting the scope and framework of future market entry agreements.Introduction and Utilization of High Priced HCV Medicines across Europe; Implications for the FutureTargeting improved patient outcomes using innovative product listing agreements: a survey of Canadian and international key opinion leadersPayers' Views of the Changes Arising through the Possible Adoption of Adaptive PathwaysReconciling uncertainty of costs and outcomes with the need for access to orphan medicinal products: a comparative study of managed entry agreements across seven European countries.Routine real-time cost-effectiveness monitoring of a web-based depression intervention: a risk-sharing proposal.Economic evaluation of brentuximab vedotin for persistent Hodgkin lymphoma.Use of product listing agreements by Canadian provincial drug benefit plans.Product listing agreements (PLAs): a new tool for reaching Quebec's pharmaceutical policy objectives?Ongoing measures to enhance the efficiency of prescribing of proton pump inhibitors and statins in The Netherlands: influence and future implications.Market access of cancer drugs in European countries: improving resource allocation.Insulin glargine in a Brazilian state: should the government disinvest? An assessment based on a systematic review.Pricing and reimbursement frameworks in Central Eastern Europe: a decision tool to support choices.The Implementation of Managed Entry Agreements in Central and Eastern Europe: Findings and Implications.Pricing and reimbursement experiences and insights in the European Union and the United States: Lessons learned to approach adaptive payer pathways.How Can Pricing and Reimbursement Policies Improve Affordable Access to Medicines? Lessons Learned from European Countries.Drug Pricing in South Korea.The intriguing future of pharmacoepidemiology.Towards a Transparent, Credible, Evidence-Based Decision-Making Process of New Drug Listing on the Hong Kong Hospital Authority Drug Formulary: Challenges and Suggestions.
P2860
Q26779553-18E53DF7-B436-4FC4-A476-A5BAFEA260B0Q27027259-24E82ECC-832C-4E2E-B5E9-EF74E1574D02Q31058117-08A031E1-2F39-4E28-AE15-A6DBB1FC14BDQ31081502-8453152C-B513-4B11-824A-1AC175D8FAB0Q33664087-7A7BBE0E-EA41-430E-933F-2E3F1122B594Q33730353-58172859-4FE2-4D29-949C-0B22419DC63DQ33730376-A4119DF7-324D-4701-9AAC-DFC76D0C00DBQ34044177-415A2FA0-3692-4270-BA0D-45EE5A9FC8E0Q34524056-E5062E57-33C2-4962-A24B-1D6BC354DEBAQ34567661-3A398E13-2D93-42A0-B6B1-2967D5215CBBQ34729037-5D985FCC-FDEB-4889-8D6A-FFF7CF1369C1Q34938911-A667F1A6-FF70-47B2-8841-F0A391C1BEA0Q35155250-342B348C-4F35-480C-A543-50F281B81AF2Q35176587-3A33976B-5410-4BE6-BAC0-DA794E8E7195Q35454428-E6C50A93-BCC4-4065-ADDC-B71203C7516AQ35522232-EB4BCB40-545E-4B3C-B37B-5197B2203FB7Q36000247-483E2866-39A3-4676-980F-9F16B701B44AQ36110773-8FADA866-A911-4965-89FC-DC312B9E4633Q36317043-A8D23FE1-B0E7-42EC-AC81-354FAFA464CBQ36714663-A9FD9910-4859-4083-B8DD-2AE9857D957CQ36841028-4568BD70-A046-4739-A78D-014AF8B9726DQ36897824-E0C2F482-DF52-40C6-B8CD-12920F24E039Q37135584-B7D054D5-DCC5-4B76-9E59-B299C01CD4C9Q37225782-F2601420-0ED8-4B3F-846A-7235883D6A25Q37290101-D80CF458-2E95-4E70-A2F1-721B2250D7E9Q37441285-0D604C2E-EEBE-4FB6-AAFD-FA195A24CEF5Q37653487-E73D06B2-4122-4059-9BDD-AEAEF9FFEF4DQ37672032-7D0580E0-FBDA-4D45-9595-F8F3FACF7204Q37723077-A0C4D8E4-B30D-44C5-96A0-93F2AE1608BDQ37723123-85A2E474-D6EA-4619-8DF8-DB2CCCF15605Q38162866-BDEE9B1E-A9F6-454B-A3A9-CA63741B3E37Q38163486-CB45F2B9-2D92-4FA4-8808-1624EA59CFD8Q38175354-FBE1DB79-D56C-4A0F-8271-BB51A582F6A5Q38223213-5CE6B9A5-20E0-43F6-9BE3-4DE0DC0E81B9Q38610858-343CA052-A53D-4ABE-A562-A50D230186C6Q38954063-155E0422-5460-4432-95C8-F5470CE751A0Q39072439-AFFEDD55-D104-4E62-A401-D491EA0AFD4AQ39110814-5E99482D-AF6E-44FA-9989-62D1692977CBQ39422831-BDA47AB9-940D-4E43-B152-616A83BBC3D5Q39432116-220169EC-2E91-4B6B-B0B1-2D3A1AE84E65
P2860
Risk sharing arrangements for pharmaceuticals: potential considerations and recommendations for European payers.
description
2010 nî lūn-bûn
@nan
2010 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Risk sharing arrangements for ...... endations for European payers.
@ast
Risk sharing arrangements for ...... endations for European payers.
@en
type
label
Risk sharing arrangements for ...... endations for European payers.
@ast
Risk sharing arrangements for ...... endations for European payers.
@en
prefLabel
Risk sharing arrangements for ...... endations for European payers.
@ast
Risk sharing arrangements for ...... endations for European payers.
@en
P2093
P2860
P356
P1476
Risk sharing arrangements for ...... endations for European payers.
@en
P2093
Alan Haycox
Bogusława Osińska
Brian Godman
Catherine Sermet
Corrine Zara
Gabriella Ofierska-Sujkowska
Harald Herholz
Jakub Adamski
Kamila Wendykowska
Kristina Garuolienè
P2860
P2888
P356
10.1186/1472-6963-10-153
P577
2010-06-07T00:00:00Z
P5875
P6179
1049104756