The Organizing Committee is delighted to invite you to attend the 7th European Biosimilars Congress one of its remarkable Pharmaceutical conferences, to be held during May 15-17, 2017 in Munich, Germany. European Biosimilars Congress 2017 brings together scientists, researchers and CROs from around the world. With the approval of second biosimilar by the USFDA-Inflectra the biosimilars market is owned to experience a exponential growth over the coming few years. Many biologics products are making their entry in the pharma market and experiencing a notable rise in their usage over the conventional medications.
At Euro Biosimilars 2017 meet your target audiences from around the world focused on learning about biologics and biosimilars. This conference would be your single best opportunity to reach the largest assemblage of participants from the biologics and biosimilars community.
Why to attend???
Conduct demonstrations, distribute information, meet with current and potential Scientists to update yourself with latest technological advancememts and new research, and receive name recognition at this 3-days' event. World-renowned speakers, the most recent techniques, tactics, and the newest updates in the era of follow-on-biologics and biosimilars are hallmarks of this conference.
Target Audience:
Directors, CEO’s of Organizations
Business Development Managers
Chief Scientific Officers
R&D Researchers from Biosimilar and Bioslogics Industries
Professors, Associate Professors, Assistant Professors
PhD Scholars
Patent Attorneys
Intellectual Property Attorneys
Investment Analysts
Association, Association presidents and professionals
Noble laureates in Health Care and Medicine
Bio instruments Professionals
Bio-informatics Professionals
Software development companies
Research Institutes and members
Supply Chain companies
Manufacturing Companies
CRO and DATA management Companies
Training Institutes
Business Entrepreneurs
Market Analysis
As per market researchers, the global biosimilar market is expected to be worth $24 billion in 2019-at compound annual growth rate (CAGR) of some 65% from 2014.Clinical trials at global level would incur an approximate cost of few hundred crores.The estimated cost of developing biosimilars for global markets is $75-250 million, while developing traditional non-biologic generics costs about $2-3 million. With the introduction of Inflectra on April 06, 2016 the Biosimilar Market will grow at even higher rate.
Critical Analysis:
The capital-intensive nature of the biosimilar business and long gestation periods between initial investment and commercialization require biosimilar players to take a higher level of risk than their counterparts in the smallmolecule generics business, and this can be a significant barrier to entry for many start-ups.
Importance & Scope:
The European-based pharmaceutical industry makes a major contribution to the Europe, not just in financial terms but also in terms of high-trait employment. Globally Pharma Market ranges from $870-$900 billion and in Europe $260-$280 billion.
All accepted abstracts will be published in respective Conferenceseries International Journals.
Current Challenges of Biologics
Quality by Design for Biologics and Biosimilars
Early clinical development essentials
Late clinical development essentials
Drug safety essentials
Comparability for biologics
Unique considerations for biologics
Advertising, promotion and labeling essentials
Implimentation of the BPCI Act
Biopharmaceuticals development
Emerging Biosimilars in Therapeutics
Biologics in cancer
Biologics for psoriasis
Biologics in genetic disorders
Biosimilar monoclonal antibodies
Recombinant therapeutic proteins
Insulin biosimilars
Biologics in autoimmune disease
Analytical Strategies for Biosimilars
Biosimilar multimodal techniques
Biosimilar bioanalytical methods
Bioassay for comparability and potency testing
Biosimilar LC/MS analysis for discovery, preclinical,
Biosimilar GMP protein analysis
Biosimilar electrophoresis
Regulatory Approach and Legal Issues of Biosimilars
Licensing of biosimilars
BLA filing for biosimilars
Regulatory prospects of BRIC countries
Biowaiver approval for biosimilars
Patent protection and infringement issues
Market exclusivities
Patent negotiation and litigation phase
Innovative Approach for Biosimilars
Next generation biosimilars
Future of biosimilars
Application of biotechnology in pharmaceutical prod
Consequences of Brexit on Biosimilars
Brexit- Pros and Cons to European pharma market
Post Brexit changes in Biosimilars regulation in UK
Fate of biosimilars clinical trials in UK
Research funding from European organizations to UK
Globalization of Biosimilars
Global impact of biosimilars over generics
Biosimilars in global market
Cost and risk management
Adopting innovative mechanisms such as risk-sharing
Global P&R models for the biosimilars and generics
Clinical Development of Biosimilars
Biosimilars Clinical Trials
Clinical PK/PD studies
Toxicological studies
Risk management, and quality affairs
Targeted cell line development
Case studies and clinical models
Biologics Product Life Cycle and Sustainable Market
Biologics Product Life Cycle and Sustainable Market
Biosimilar Market and Cost Analysis
CAGR of biologics and biosimilars in Europe
Penetration and uptake of biosimilars in different
Biosimilars Pharmacoeconomic Modelling
Return on Investment(ROI) for Biosimilars
Pharmacovigilance on Biosimilars
Problems in biosimilar pharmacovigilance
Adverse drug reactions with biologics and biosimil
Detection and evaluation of drug safety signals
Entrepreneurs Investment Meet
05月15日
2017
05月17日
2017
注册截止日期
留言