
doi: 10.1038/nbt.2438
pmid: 23222784
For authorized biosimilars to achieve full acceptance in the marketplace, it is crucial that they are considered to be therapeutically equivalent and interchangeable with the brand reference product.
Risk Management, Therapeutic Equivalency, Humans, EMC OR-01-34-01, European Union, Biosimilar Pharmaceuticals, Drug Approval, Biotechnology
Risk Management, Therapeutic Equivalency, Humans, EMC OR-01-34-01, European Union, Biosimilar Pharmaceuticals, Drug Approval, Biotechnology
| citations This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | 90 | |
| popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network. | Top 10% | |
| influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Top 10% | |
| impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Top 1% |
