On 27 March 2015, the European Medicines Agency (EMA) published its reflection paper for follow-on versions of iron-based nano-colloidal products. The agency first released the draft reflection paper for follow-on versions of iron-based nano-colloidal products for a three-month consultation period in September 2013.
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- South Korean companies to make generic Bridion and COVID-19 drugs
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- Cancer and diabetes generic treatments receive positive opinion from EMA’s CHMP
- What is the meaning of a narrow therapeutic index?
- Consequences of generics being favoured by healthcare providers
- What is meant by a generic medication and generic equivalence?
- The cost of developing drugs and use of generics
- FDA approves pegfilgrastim and rituximab biosimilars
- Byooviz: first ophthalmology biosimilar launches in US
- Biocon: cancer biosimilar launch in Canada and US$90 million Malaysia deal
- Canada approves five biosimilars in last seven months
- No trends in biosimilars uptake levels in the US, reveals study
- El impacto de las insulinas biosimilares en el gasto público brasileño
- Challenges with implementing benefit-sharing programmes for biologicals in Europe
- Successful increase of biosimilar adoption in a large integrated health delivery network
- Estado actual de los biosimilares de anticuerpos monoclonales aprobados en América Latina
- Una visión general de los biosimilares de anticuerpos monoclonales en América Latina
- American Academy of Ophthalmology biosimilars position statement published
- US prescription drug expenditure projection report
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