Rezultati pretraživanja
  1. 3. lis 2019.

    PhUSE SDE at Merck was a blast. Kevin Lee discussed the 21st Century Review Cycle & the FDA rejection processes. He also presented how biometric departments should use for FDA compliant submission. Contact us with any questions regarding e-Submission.

  2. prije 14 sati

    ¿Sabías que somos la única empresa española que ha desarrollado un software generador de los formatos y ? LATOK, al servicio de la desde 2009.

  3. 4. velj

    We are ready for the technology-driven era of regulatory, are you? Meet Cunesoft, a Phlexglobal company, at the ! Talk with our experts –get to know what your future technology provider can offer you!

  4. 4. velj
  5. 1. velj

    Taat kepada syariat merupakan jalan kemuliaan >> << -

  6. 1. velj

    Hijabmu adalah tanda pengenalmu wahai Muslimah >> << .

  7. 1. velj
    Odgovor korisniku/ci

    Ajakan untuk tdk berhijab harus di tolak, karena bermaksiat kepada Alloh. >> << .

  8. 1. velj

    Melaksanakan perintah karena kita tak tau yang datang terlebih dahulu AJAL atau HIDAYAH >> << .

  9. 1. velj

    Aurat harus ditutup itu wajib gaeeeeessssss.... >> << .

  10. 1. velj
    Odgovor korisniku/ci

    Hijabmu adalah kehormatan mu, mulia dengan hijab mu. >> << - RT

  11. 30. sij

    Coming to the DIA’s ? Visit Cunesoft & Phlexglobal at booth 211! Let’s have a great conversation where you can learn more about the future of the world and dive deep into !

  12. 29. sij

    As of the 1st January 2020! For support in managing your get in touch!

  13. 24. sij
  14. 17. sij

    Only two months to go! We're excited to be exhibiting at . If you are into , don't miss our "see too" booth :) Visit us at to say "hi" and forge new partnerships. 17-19 March 2020 in Brussels.

  15. 27. stu 2019.

    Interessanter Beitrag zum Thema -Zulassung, via :

  16. 21. stu 2019.

    Register now for our complimentary webinar on the new EAEU electronic submission format:

  17. 24. lis 2019.

    Mono experts held a practical, hands-on, CTD and training in , . Topics ranging from what is eCTD and how get prepared for electronic submission to how to solve most common validation issues using real-world scenarios.

  18. 23. lis 2019.

    Visit our website today to watch a product preview and to learn more about the only electronic submission Authoring Template Suite created BY writers FOR writers:

  19. 15. lis 2019.

    Today is the last day to receive early bird pricing on the upcoming Intermediate Course on eCTD Regulatory Submissions, 14-15 November in Rockville, MD. Save your spot -

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