Coalesce
Research Group invites all pharmaceutical and Medical
researchers, professionals, faculties and students the from across the globe to
attend “International Conference on Biosimilars and Biologics” during April
20-21, 2020 at Dubai, UAE which
includes keynote presentations from highly affiliated personalities, Oral
talks, Poster presentations and Exhibitions.
ICBB-2020 focuses upon “The
Present Scenario and Future Prospects of Biosimilars & Biologics”.
This biologics meeting focuses on the trends which the biosimilar
markets is heading on since its launch till the present date and moving on to
the projections in future. It takes into its fold the critical developmental
procedures, analyses, regulatory factors and also pharmacovigilance including
post marketing surveillance and clinical studies. Innovation and compliance to
regulatory guidelines are the most critical aspects towards biosimilars and
follow on biologics development and successful launching to the market.
HIGHLIGHTS
Current Challenges in
Developing Biosimilars and Biologics, Emerging Biosimilars in
Therapeutics, Biosimilars Analytical
Strategies, Regulatory Approach for
Biosimilars, Globalization of Biosimilars, Biosimilars Role in Oncology
and Gastroenterology, Biologics and Biosimilars in
inflammatory bowel disease, Biosimilars vs Biologics, Biosimilars vs Generics, Biologics as therapeutics, Immunogenicity of
Biosimilars, Intellectual Property Rights, Monoclonal Antibody and
Fusion Protein Biosimilars, BCS and IVIVC Based
Biowaivers, Biosimilar Companies and
Market Analysis, Legal Issues and BPCI ACT, Biosimilars Research
Pipeline, Bioequivalence Assessment, Biopharmaceuticals and
Biotechnology, Current Trends in
Pharmaceutical industry and Biosimilars in Rheumatology
and Dermatology
Conference Website: https://coalesceresearchgroup.com/conferences/biosimilars-biologics
Abstract Submission: https://coalesceresearchgroup.com/conferences/biosimilars-biologics/abstractsubmission
Registration: https://coalesceresearchgroup.com/conferences/biosimilars-biologics/registration
WHY ATTEND?
At the moment, the uptake of biosimilars
is still limited, especially in the US due to a lack of confidence towards
biosimilars by some stakeholders; uncertainty about the interchangeability and
substitution of biosimilars; and a hospital financing system that discourages
the use of them. This year’s conference gathers biosimilars main players in the
industry, representatives of pharmaceutical and biotechnological companies,
professionals from governments, physicians and researchers to discuss updates
in biosimilars’ development and regulatory restraints around them.
Professionals and leaders will join an open conversation about barriers in
developing biosimilars, cost of developing biosimilars; additionally, discover
the way to introduce biosimilars to the market and provide sufficient knowledge
for potential customers and consumers. Attendees will have the opportunity of
networking with experts in the field while learning and sharing analytical
views of the current biosimilars scene.
KEY
PRACTICAL LEARNING POINTS OF THE SUMMIT
- An overview of the current biosimilars market
- Barriers in developing biosimilars
- Cost of developing biosimilars
- A summary of regulatory pathways in various geographic regions
- How biosimilars is developing in different countries
- An overview of approved biosimilars in the E.U., U.S., India, South Korea and Latin America.-
- The market impact of biosimilars on their reference biologics
- The top ten biologics on the focus of biosimilar developers
- Ways to commercialize biosimilars
- Implications of biosimilars in patient treatment
WHO
SHOULD ATTEND
CEOs | CIOs|VPs | CTOs|
Directors|Department Heads|Technical Analysts|Research Engineers |Specialists|
Government officers specializing in:
·
Bioequivalence assessment
·
Biopharmaceuticals
·
Biologics/Biotechnology/ Biogenerics
·
Biosimilars Legal Affairs
·
Drug Pricing and Reimbursement
·
Regulatory Compliance
·
Preclinical and Clinical Development
·
Quality Affairs/ Quality Control
·
Biopharmaceuticals
·
Intellectual property
·
Clinical Immunology
·
New Product Development and Pharmacovigilance
·
Clinical Immunology
·
Immunology
·
Drug Safety
·
Preclinical Development
·
Vaccines Development
·
Validation
·
Analytical Characterization
·
Antibody Discovery
·
Oncology
·
Infection and Immunity
·
Risk Management
·
Clinical Program
·
Personalized Medicine
·
Portfolio Planning
·
Regulatory Affairs
·
Pharmacovigilance
·
Global Strategy and Antibody Engineering
TARGET
AUDIENCE
·
Pharmaceutical Companies,
·
Pharma Associations & Societies,
·
Biotechnology Experts/Business Entrepreneurs.
·
R&D, F&D Scientists
·
Intellectual Property Attorneys
·
Ph.D. and Post Doctorate ScholarsRegards
CONTACT US
Jon Peters
Biosimilars and Biologics 2020
T: +1-718-543-9362
biosimilars@coalescemeetings.com
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