Medical Writing & Documentation Unlock the power of clear and concise trial documentation
Medical Writing & Documentation Unlock the power of clear and concise trial documentation
Save Valuable Time & Keep on Track
Wemedoo’s expert medical writing team delivers clear, compliant documentation— from protocols to study reports and publications—ensuring your clinical trials run smoothly and meet the highest standards. Let us help you streamline processes and elevate the quality of your research.
Wemedoo provides expert medical writing to support clinical trial planning, execution, and reporting. We help communicate complex medical data clearly to regulators, healthcare professionals, and the public. Whether you're a data manager, trial director, or study coordinator, our team ensures your documentation is accurate, compliant, and impactful.
The preparation of a clinical trial protocol is a complex task undertaken by a multidisciplinary team of experts. With years of experience and a deep understanding of clinical research, our PhD-level experts closely work with you to prepare a detailed and regulatory compliant study protocol.
Streamline your clinical trial documentation with Wemedoo’s expert medical writing. We deliver clear, compliant, high-quality content—saving you time while ensuring accuracy and consistency.
We deliver impeccably crafted clinical trial documents that are professionally written, clear, and concise, adhering to rigorous quality standards and reflecting our commitment to excellence.
Wemedoo saves you valuable time and resources by entrusting documentation tasks to specialized writers, allowing the clinical team to focus on core research activities.
Wemedoo’s expert medical writers turn complex clinical data into clear, accessible documents for better understanding.
We ensure uniformity in style, format, and content across all trial-related documentation, enhancing professionalism and clarity.
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Get the answers you need about our risk-based monitoring and source data review service
Our services encompass a wide range of clinical trial documentation, including clinical study protocols, study reports, regulatory submission documents and scientific publications. Additionally, our expert team provides all regulatory documentation and study plans covering our services.
Our team stays updated with the latest regulatory guidelines and incorporates these standards into every document we produce, ensuring compliance with agencies like the FDA and EMA, as well as bodies like the International Conference on Harmonisation and TransCelerate.
Absolutely. Our team of medical writers has diverse expertise across various therapeutic areas, enabling us to effectively handle writing for specialized and rare conditions.
Outsourcing saves you time and resources while maintaining your organizational flexibility. Our expert writers efficiently produce high-quality, compliant documents. This allows your team to focus on core research activities while we handle the complexities of medical writing.
We follow strict quality control procedures, including thorough reviews and validations, to ensure consistency and accuracy in all our medical writing outputs.
Wondering How It All Works?
Learn more about how we can support your clinical trials.
SPEAK TO AN EXPERT Beyond protocol development, Wemedoo offers a comprehensive suite of integrated data operations services for clinical trials. At each step, we ensure your trial meets the highest quality and regulatory standards, while streamlining your clinical trial processes and saving you time and money. Discover our other services, all focusing on innovation and excellence in clinical research.
FDA Inspection Passed Without Any Findings
Wemedoo ensures its validation procedures meet and surpass industry and regulatory standards. This underscores our commitment to software compliance, secure operations, and high-quality software.
Read more about the experiences from those who have partnered with us
All jobs, both large and small, are performed with the same dedication to quality, detail, innovative thinking, and rigor. It is always a pleasure to work with the Wemedoo team.
Georg Mathis, PhD
CEO Appletree CI Group AG
Wemedoo embodies all the traits desired in a partner in the clinical trial industry – expertise, innovation, reliability, compliance, and attention to detail.
Martina Diminic Smetisko, DMD
Managing Director at Marti Farm Ltd
Their dedication to, and support of, our projects has resulted in clear quality deliverables. They are always there to answer any questions with expertise in a timely manner. I am looking forward to our next project together.
Volodymyr Stus, MD
Biopharmaceutics and Clinical Research Department Manager at Polpharma SA
Considering Unified Clinical Trial Software?
Experience oomnia, our all-in-one clinical trial software which unifies tools, such as EDC, eSource, RTSM, eTMF, ePRO, eCOA, eConsent, and CTMS. In combination with our professional services, we can provide end-to-end support to transform your clinical research.
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