154,79 €
Biosimilar Drug Product Development
Biosimilar Drug Product Development
  • Išparduota
Biosimilar Drug Product Development
Biosimilar Drug Product Development
El. knyga:
154,79 €
When a biological drug patent expires, alternative biosimilar products are developed. The development of biosimilar products is complicated and involves numerous considerations and steps. The assessment of biosimilarity and interchangeability is also complicated and difficult. Biosimilar Drug Product Development presents current issues for the development of biosimilars and gives detailed reviews of its various stages and contributing factors as well as relevant regulatory pathways and pre- and…
  • Leidėjas:
  • Metai: 2017
  • Puslapiai: 487
  • ISBN: 9781351646185
  • ISBN-10: 1351646184
  • ISBN-13: 9781351646185
  • Formatas: ACSM ?
  • Kalba: Anglų

Biosimilar Drug Product Development (el. knyga) (skaityta knyga) | knygos.lt

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154,79 € El. knyga

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When a biological drug patent expires, alternative biosimilar products are developed. The development of biosimilar products is complicated and involves numerous considerations and steps. The assessment of biosimilarity and interchangeability is also complicated and difficult. Biosimilar Drug Product Development presents current issues for the development of biosimilars and gives detailed reviews of its various stages and contributing factors as well as relevant regulatory pathways and pre- and post-approval issues.

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  • Leidėjas:
  • Metai: 2017
  • Puslapiai: 487
  • ISBN: 9781351646185
  • ISBN-10: 1351646184
  • ISBN-13: 9781351646185
  • Formatas: ACSM ?
  • Kalba: Anglų

When a biological drug patent expires, alternative biosimilar products are developed. The development of biosimilar products is complicated and involves numerous considerations and steps. The assessment of biosimilarity and interchangeability is also complicated and difficult. Biosimilar Drug Product Development presents current issues for the development of biosimilars and gives detailed reviews of its various stages and contributing factors as well as relevant regulatory pathways and pre- and post-approval issues.

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