Biosimilars Conference 

Conference; Wednesday 25 and Thursday 26 September 2019, Workshop: Tuesday 24th September 2019, Copthorne Tara Hotel, London, UK

The event’s focus is to highlight the current challenges in the biosimilars market and discuss current undergoing plans or developments to overcome these challenges.

The biosimilars market is forecasted to reach USD$23.6B by 2023 at a compound annual growth rate (CAGR) of 31.70%. Factors driving the increase of this market include growing demand for biosimilar drugs due to their cost-effectiveness, growing incidence of chronic diseases, and strategic collaborations resulting in enhanced productivity and clinical trial activities.

With the expiry dates of major patents fast approaching, the emerging gap in the market for biosimilars is now a major attraction for manufacturers. As the availability of biosimilars could potentially reduce direct spending by USD$54B by 2026, the question is what can current biosimilar producing companies do to join this market to benefit the patients, physicians and investors?

 BENEFITS OF ATTENDING

  • HEAR about current strategies under development to overcome challenges with patents currently faced by many biosimilar developers
  • DISCUSS the possible changes in regulatory approval of biosimilars in the UK post Brexit, and how this will impact market entry
  • EXPLORE the latest methods in use to maintain the relationship between stakeholders, doctors and patients, with the influence of governing bodies
  • REVIEW FDA regulations for the approval of Biosimilars and the latest approvals

PLUS TWO INTERACTIVE HALF-DAY PRE-CONFERENCE WORKSHOPS

Tuesday 24th September 2019, Copthorne Tara Hotel, Central London, UK

 A: Interchangeability in the USA: The US-FDA Regulatory Guidance

08.30 - 12.30

Workshop Leader: Michel Mikhail, International Expert Regulatory Affairs, Global Expert of Biosimilars

B: Advancing Biosimilars Development and Uptake in MENA & GCC Regions

13:30 – 17:30

Workshop Leader: Rodeina Challand, General Manager, Challand Biosimilar Consulting

 WHO SHOULD ATTEND?

Presidents, Vice Presidents, Managing Directors, Directors, Associate Directors, Chiefs, Heads, Principals, Managers and Analysts of:

  • Biosimilar Development
  • Product Development
  • Commercialization
  • Market Access
  • Medical Affairs
  • Intellectual Property
  • Bioloigcs
  • Biopharmaceuticals
  • Research and Development
  • Generics
  • Biobetters
  • Business Development
  • Strategic Marketing
  • Drug Development
  • Clinical Trials
  • Immunogenicity Studies

Global Presence: Attendees from all over the world attend our events. Gain hands on insight from representatives from UK, Europe and USA.

For details and to register, visit the website at www.biosimilars-europe.com/farmavitawl 

 

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