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The Biosimilars Alliance

The Biosimilars Alliance – Benefits

Benefits of leveraging The Biosimilars Alliance:

The Biosimilars Alliance team members include experienced:

 

  • Pharmacologists/Toxicologists
  • Bioanalytical scientists
  • Certified project managers
  • Clinical pharmacologists and therapeutic area experts
  • Former regulatory agency reviewers
Two global laboratories located in Europe (Zurich, Switzerland) and the USA (Lincoln, NE)
  • Small and large molecule assays, biomarkers and immunogenicity tests
  • Only CRO with global harmonized electronic laboratory notebook
  • Technologies include: ELISA, RIA, ECLA, Luminex, LC-MS/MS
Global, GLP compliant preclinical laboratory in Lyon, France with more than 40 years of experience in Drug Safety Assessment
  • Conducts more than 40% of business with biologics
  • State of the art technologies for study performance and on-time reporting.
  • Specialization in parenteral routes of administration
Four global clinical Phase I and IIa facilities located in Europe (Belfast, Northern Ireland, UK) and the USA (Lincoln, NE; Neptune, NJ; Phoenix, AZ)
  • Over 730 beds (including 24 in-hospital) and conduct over 200 complete studies annually
  • Executed over 6,000 Phase I studies conducted globally

See also…

Press Release: Celerion and Ricerca Biosciences announce “The Biosimilars Alliance” to offer clients a more effective development path for biosimilars.

Presentation: Early Stage Studies of Biosimilars

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