OR WAIT null SECS
October 19, 2010
Pfizer announced this his week that it had entered into a strategic global agreement for the worldwide commercialization with the Indian biotechnology company Biocon (Bangalore) for biosimilar versions of insulin and insulin analog products (e.g., recombinant human insulin, glargine, aspart, and lispro).
October 07, 2010
FDA to Hold Public Hearing on Biosimilars Legislation, And More.
September 16, 2010
The generic-drug company Actavis (Hafnarfjordur, Iceland) is considering acquiring a 51% stake in the biopharmaceutical company BioPartners Holdings (Barr, Switzerland) from Bioton, a Polish biotechnology company.
September 10, 2010
Director General of the European Generic Medicines Association (EGA), Greg Perry, has emphasised the need for EU biosimilar guidelines for monoclonal antibodies (mAbs), as well as a harmonised, global approach to biosimilars in general, at the agency's 8th International Symposium on Biosimilar Medicines.
September 09, 2010
Director General of the European Generic Medicines Association (EGA), Greg Perry, has emphasized the need for EU biosimilar guidelines for monoclonal antibodies (mAbs), as well as a harmonized, global approach to biosimilars in general, at the agency's 8th International Symposium on Biosimilar Medicines.
September 01, 2010
A Strengths, Weaknesses, Opportunities and Threats analysis of the biosimilars market is given.
Both biosimilar and generic drugs have an abbreviated approval process; however, the clinical trial requirements differ enormously.
In light of the impressive size and predicted growth of the market, there has been a rising interest in the development of biosimilars.
Many hurdles lie between a biosimilar and success on the market. In particular, there are three main questions that companies will be asking themselves.