ABSTRACT The medical and pharmaceutical industries must commit to full consensus on biosimilar products. Regulatory recommendations and current resources applied to biosimilars should not be squandered. Additionally, continued lessons learned… Click to show full abstract
ABSTRACT The medical and pharmaceutical industries must commit to full consensus on biosimilar products. Regulatory recommendations and current resources applied to biosimilars should not be squandered. Additionally, continued lessons learned should be applied for the preparation of future unknown classes of medical treatments. Recommendations from provider consensus are sound, logical, and feasible. These should be set forth, implemented and agreed upon globally.
               
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