Rezultati pretraživanja
  1. 22. sij

    Global Head of Transparency & Disclosure, , delving in to prospective & retrospective analyses of clinical disclosure & data sharing requirements.

  2. 15. kol 2019.

    Now: , President of Patient Advocates in Research (PAIR) speaks to the attendees on what and transparency look like from a patient’s view.

  3. 19. srp 2019.

    Clinical trial is an important topic globally. Our unique transparency course offering provides students the technical skills to meet global requirements:

  4. 25. tra 2019.

    Regulatory Public Disclosure Special Interest Group (RPD SIG) meets Thu 9 May 19, 1 - 1.30 pm @ EMWA Conference, Vienna - FREE lunchtime session. You are warmly invited to discuss RPD matters and share info.

  5. 8. velj 2019.

    MMS University has partnered with to provide medical writing and clinical trial disclosure courses to students. Learn more about our partnership here

  6. 6. velj 2019.

    MMS University's unique course provides students with technical skills to meet global trial disclosure requirements. Learn more here

  7. 22. sij 2019.

    VIDEO: Did you know that our 16-week Clinical Trial Disclosure course provides in-depth knowledge of managing and supporting disclosure requirements across the globe? To learn more, watch our video:

  8. 7. sij 2019.

    MMS University's 16-week Clinical Trial Disclosure course provides in-depth knowledge of managing and supporting disclosure requirements across the globe. Watch our video to learn more:

  9. 27. pro 2018.

    More than 290,000 studies are registered on in all 50 states and across 206 countries. To see how clinical trial disclosures are expanding globally, View our FREE infographic:

  10. 17. pro 2018.

    VIDEO: Did you know that our 16 weeks' course provides in-depth knowledge of managing and supporting disclosure requirements across the globe? Watch the video now to know more:

  11. 6. pro 2018.

    Our proprietary Compliance Calculator gives pharma and academia insight into their level of compliance with the reporting of study results to . Try it free, with no obligation, here:

  12. 29. stu 2018.

    This one-of-a-kind course provides background perspective and technical skill sets for facilitating workflow and summarizing data to meet global trial disclosure requirements. Learn more:

  13. 28. stu 2018.

    Regulatory disclosures needs are constantly increasing. This infographic helps break down the numbers. Read more here:

  14. 20. stu 2018.

    With enterprise solutions, the Workflow Lead facilitates study team review, QC checks, approval processes, registry submissions, and responds to queries from governing bodies. Learn more about TrialAssure's solutions here:

  15. 13. stu 2018.

    Q&A: Learn why Zach says “…in the future all the global registries will be integrated on a single platform that is searchable in any language.” Find out now:

  16. 12. stu 2018.

    MMS University's 16-week course provides in-depth knowledge of managing and supporting disclosure requirements across the globe. Watch the video here:

  17. 8. stu 2018.

    Did you know that 1 of every 3 global studies are subject to duplicate entry in more than 10 different global trial registries? Simplify with our ultimate transparency suite and request a free demo today:

  18. 7. stu 2018.

    TrialAssure provides implementation support to get you up and running, including systems integration, data migration, and customized role-based training. Read more about our software licensing here:

  19. 24. lis 2018.

    With TrialAssure, you can submit information tailored to , EudraCT, or any other global trial registry from a single data record. Learn more about our software features:

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