Zoekresultaten
  1. What is required to demonstrate analytical similarity for compared to their reference products? Watch Dr. Steve Kozlowski explain the data requirements.

  2. 7 uur geleden

    ' provide the NHS with the prospect of saving millions of pounds, whilst also increasing access to important medicines'- looks at how adoption of the products can be sped up

  3. 8 uur geleden

    Check out these 2 FREE activities on to treat inflammatory diseases & in just 15 mins per webcast, you’ll gain new insights on these new treatment strategies & earn / credit. Find them (& more) on the Biosimilars Hub:

  4. 8 uur geleden
  5. 10 uur geleden

    Most of the recent on issued by have been related to manufacturing facility short comings, rather than on the clinical/safety/physiochemical data. Can't say actually that the FDA regulatory requirements are stricter though.

  6. 10 uur geleden

    Thank you for your hard persistent work in getting this legislation signed! You absolutely rock! 👍🏼💙 Biosimilar Substitution Victories Across the Country! Now on to more states! 💪🏼

  7. 28 jun.
  8. 28 jun.

    Join Us! Submit your entry before 13th July for a chance to be recognized at this year . Celebrating the efforts made by the & industries, in making more affordable readily available to all. Enter:

  9. 27 jun.

    IPCs Biosimilars@working group just finished an exciting day of presentations discussing a variety of topics. Looking forward to an updated manuscript from the team.

  10. 27 jun.

    Lees over Congresnieuws, registraties en marktontwikkelingen op het gebied van in de van Biosimilars Nederland van juni 2018

  11. 27 jun.

    Presentation by researchers of On topics addressed in the field of .

  12. 27 jun.

    Jonathan Kay, MD presents current approved for at the IPC Biosimilars round table at in Stockholm.

  13. 27 jun.
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  16. 26 jun.

    At the unveiling of the official “Switch Management between Similar Biological Medicines” for nurses by

  17. 26 jun.

    - Global Regulatory Strategies for Biosimilars panelists agreed on need for global harmonization for distinct non-proprietary names

  18. 26 jun.
  19. 26 jun.

    Medaxes participating in debate organised in . Supporting strong industry in Europe, creating pharma eco-systems to the benefit of European workers and their companies, whether , or manufacturing waiver

  20. 25 jun.

    Learn about and the obstacles smaller companies face when trying to bring them to market in this session chaired by Oxana Iliach - tomorrow at 8am.

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