CSOFT Webinar: How to Successfully Conduct Overseas Clinical Trials as a Small-Medium Sized Biopharmaceutical Company

November 17, 2021

BOSTON, MA, November 17,2021. In this free webinar, our panelists Dr. Vladimir Misik and Joshua Maislin, will discuss current and future major clinical trial trends as well as important clinical trial strategy questions for small-medium Biopharmaceutical companies. In addition, the audience will be able to learn more about the importance of regulatory compliance and safety content translation as well as challenges and solutions for getting ready to enter foreign markets.

Dr. Vladimir Misik, Partner & Founder at LongTaal, will outline the top criteria and important factors for small-medium sized Biopharma companies looking to expand their ROI and development outside of major markets, including industry market trends and opportunities for growth. Dr. Misik will also quantify the nature of clinical trial (CT) industry investment and predict which markets will see the most growth in the coming future.

Joshua Maislin, Sr. Customer Success Manager at CSOFT Health Sciences, will discuss how small-medium sized Biopharma companies can leverage best practices to ensure all technical documentation, patient safety reports and data, and other important aspects are translated and compliant with relevant regulatory bodies.

Join Dr. Misik along with  Joshua Maislin, in the live webinar on Monday, November 22, 2021 at 11:30am EST (4:30pm GMT/UK) to learn more about clinical trial industry investment and market competitiveness.

For more information, or to register for this event, visit How to Successfully Conduct Overseas Clinical Trials as a Small-Medium Sized Biopharmaceutical Company.

About CSOFT Health Sciences

CSOFT Health Sciences, leaders in medical translations, provides end-to-end medical translation services for all phases of the product lifecycle, from pre-clinical to post-launch. We also specialize in market access consulting, medical writing, and CTD/eCTD submissions with the FDA, EMA, and NMPA. Our operations are certified in ISO 9001:2015 and ISO 13485:2016, ensuring our customized solutions meet the rigorous regulatory requirements of global submissions. Learn more here.

Media Contacts:

  • Nikki Andrews (U.S./Europe)

Phone: +1 (617) 263-8950

Email: nikki.andrews@csoftintl.com

  • Tim Wang (Asia)

Phone: +86 21 3106 3376

Email: tim.wang@csoftintl.com

ABOUT XTALKS

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To learn more about Xtalks visit http://xtalks.com

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