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Advanced Therapies Congress
Meet Veristat at the Advanced Therapies Congress 2025
Veristat is excited to participate in the Advanced Therapies...
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As medical content evolves from focusing on technical and scientific information to also incorporating patient- and consumer-targeted communication, and as the range of regulatory documents expands, medical writing remains a highly valued and in-demand service for Veristat clients.
What constitutes effective medical writing in clinical research? Dr. Sarah Hopwood, Vice President of Global Medical Writing at Veristat, outlines how our medical writers’ unique skill set, extensive experience, and commitment to staying up to date with industry regulations contribute to the success of our sponsors.
Helping Sponsors Communicate the Value of Their Data Globally
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Why is medical writing so important throughout the product development lifecycle? Because every piece of written documentation included in a regulatory submission can impact the review and approval process. Veristat’s expert medical writers ensure documents are of high quality; that complex scientific information is communicated clearly and accurately, improving the chances of a successful application and reducing the risk of delays. We emphasize the efficacy and safety of new therapies, positioning them for success. We see effective medical writing as the bridge between science and successful regulatory outcomes. And at Veristat, we are dedicated to making that bridge as strong and dependable as possible.
Veristat medical writers are highly qualified scientists with most team members holding a Ph.D. or other advanced degrees. With an average of 11+ years of industry experience, 80% of the team has written for rare or ultra-rare diseases. Our team has extensive experience in meeting the requirements of regulatory bodies worldwide, in Europe and the United States in particular, with mastery in a wide range of medical writing deliverables including clinical trial and regulatory documents, medical device documents, publications and other medical communications, as well as patient-friendly communications. We take pride in ensuring that all content is of high quality, accurate, and consistent.
Listen as Sarah describes the skills and capabilities of Veristat’s medical writing team: Sarah Hopwood - What Makes a Successful Medical Writer?
Staying on Top of the Regulations
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Regulations are constantly evolving, with new guidance documents and requirements emerging in response to clinical, scientific, and technological advancements. The complex regulatory landscape can be overwhelming for sponsor teams responsible for preparing the numerous documents required for a regulatory filing. With support from our experienced medical writers who understand global industry regulations and who are dedicated to delivering documents of exceptional quality, you, as a sponsor, can better control all aspects of your submission. Veristat medical writers complement our sponsors’ teams with a comprehensive understanding of evolving global industry standards, ensuring adherence to preferred formats and terminology so that you can be confident that compliance is never a concern.
Regardless of the regulatory authority, a submission is fundamentally dependent on the ability to effectively convey a therapy's value. Veristat medical writers deliver this through clear, concise communication that adheres to all applicable industry regulations and guidance.
Listen as Sarah describes how Veristat’s medical writing team stays on top of the regulations: Sarah Hopwood -MW- Staying Updated On Changing Regulations
Want Ready to learn more about Veristat’s approach to developing high-quality and compliant documentation at every stage of product development? Contact us today.
