13th Biosimilars Congregation 2019
Uniting industry leaders to analyse advanced commercial developments & to identify successful management strategies of Biosimilars
11th & 12th June 2019, Pestana Chelsea Bridge Hotel, London, UK
13th Biosimilars Congregation 2019 will provide insight into the current state of play in the EU and stimulate debate, in a multi-stakeholder setting, on the vital role of biosimilar medicines in the sustainability of healthcare systems. Beyond a comprehensive outlook of key European market access policies, our speakers will outline the key recent developments in regulatory science and regulatory policy in the EU and other international jurisdictions. Special emphasis will be placed on strengthening the link between regulators and medical communities as an essential basis for greater understanding and acceptance of biosimilar medicines. This Biosimilars conference will focus on multiple aspects of Biosimilar product development to successfully deliver safe, Biosimilar products to the market place. By attending this conference, you will gain a comprehensive outlook on the key issues surrounding Biosimilars. This event will provide an important platform for Biosimilars stakeholders to discuss and share best practices in furthering Biosimilars development.
KEY SPEAKERS:
SUE NAEYAERT, Global Head Government Affairs, Policy & Pharmaceconomics, Fresenius Kabi SwissBioSim
SHU-YI SU, Statistical Scientist, Novartis
IAN HENSHAW, VP, Global Head of Biosimilar Business Unit, Biogen
MAGNUS BODIN, Director, Market Access Biosimilars, Biogen
CHRISTIAN AGBOTON, Sr Global Brand Medical Director - Global Medical Affairs, Takeda
JOSEPH DUNFORD, European Biosimilar Franchise Manager, Accord Healthcare
VICTOR SASTRE, Senior MSL , Amgen Biosimilars, (Board Member MSL Society Advisory)
FREDRIK SUNDBERG, Director Strategic Customer Relations, GE Healthcare
HANMANT BARKATE, Vice President & Head Medical Services, (India, MEA), Glenmark (India)
JOSEPH SALAMEH, Medical Lead, Alnylam Pharmaceuticals
STEINAR MADSEN, Medical Director, Norwegian Medicines Agency
LOUIS BOON, CSO, Bioceros
LIZ POLLITT, Director, BPCRCS
LENNEKE DE WINTER, USP Director, Bioceros
CORNELIA ULM, VP Regulatory Affairs Biosimilars, Biotec Regulatory Consulting
KARL DAVISON, Business Development Officer, NIHR Clinical Research Network
JUSTIN STEBBING, Professor of Cancer Medicine and Oncology, Consultant Oncologist, Imperial College Healthcare NHS Trust
MARIE MANLEY, Partner, Head of the UK Life Sciences Practice, Sidley Austin
JACQUELINE MULRYNE, Counsel, Arnold & Porter LLP
KEY THEMES:
Strategies for market access and expansion by identifying key changes and future projections
Consequences of Brexit on Biosimilars
Current Challenges and Opportunities for future- Strategies in developing Biosimilars
A Clinician ́s Guide to Biosimilars in Oncology: understanding the Science of Extrapolation and Interchangeability
Biosimilars – Pricing & Market access - Bringing it faster into market
GMP, GCP, QC & R&D
Current challenges and opportunities - strategies to develop Biosimilars
Payer perspective on biológics and Biosimilars
Biosimilar Interchangeability: The newest regulation
Biosimilar - Physicians and Patients perspective
CMC, Preclinical and clinical considerations for Biosimilars and Follow-on Biologics
Impact of Technology
Commercial landscape & market access for Biosimilars: Predicts to prepare for a suceesful tomorrow
Hear case studies on biosimilars drug development from pre-clinical to clinical and the various testing required such as immunogenicity and bio-similarity tests
Research-based industry Biosimilar strategies
Considerations for the analytical similarity assessments when designing a Biosimilar development program
Determining the right investments & potential returns from Biosimilars
Latest developments in regulation to increase speed of entry and compliance
Future of next generation biosimilars
Be part of a major networking opportunity
WHO SHOULD ATTEND:-
CSOs, CMOs, Vice Presidents, Presidents, Heads, Directors, Team Leaders, and Senior Scientists from the following roles:
Biopharmaceuticals/ Biotherapeutics, Follow on Biologics/Follow on Proteins/Biosimilars, Biologics/Biotechnology/ Biogenerics, Legal Affairs, Intellectual Property, Health Economics, Pricing and Reimbursement, Clinical Immunology, Principal Scientist, Chief Scientific Officer, Process Control and Analytical Technologies, Analytical Characterisation, Regulatory Compliance, Pharmacovigilance, Drug Safety & Risk Management, Quality Affairs/ Quality Control, New Product Development, Process Science, Portfolio Management, Research & Development, Business Development, Business Operations, Scientific Affairs, Commercial Affairs, Marketing
CONFERENCE SPONSORSHIP:
Email: [email protected] or Tel: +44 2036120886
Sponsor, Exhibition Stall (Booth) and a paid Speaker Slots are also available
We also have some sponsorship opportunities available for the event, which gives you an opportunity to sponsor/speak/exhibit, and create brand awareness. In addition, the networking opportunities in focused and relevant industry gathering provide the personal contact necessary for business development efforts.
CONFERENCE REGISTRATION:
In order to Register please let us know your interests through Email: [email protected] or Tel: +44 2036120886
Introductory Offer - 3 delegate places for the price of 2 - A huge saving of £750 - (Limited seats left)
Super Early Discount (Valid Till 1st April 2019): (£750 + VAT per delegate)
Early Discount (2nd April 2019 - 12th May 2019): (£950 + VAT per delegate)
Standard Registration (13th May 2019 Onwards): (£1150 + VAT per delegate)
Get more from the event, enjoy and make the best out of our dedicated networking drinks time, meet the leading international vendors showcasing the products of tomorrow in the co-located exhibition. Expand your knowledge of the latest business models and strategies in the high-level conference.