From protocol to publication - expert writing that drives scientific impact

Medical Writing Services

At Alcedis, Medical Writing bridges the gap between science and communication. Our writers turn complex clinical content into clear, structured, and compliant documents—tailored to audiences ranging from regulators to patients. Whether for protocol development, informed consent, or scientific publication, our medical writing team ensures that every word supports your study goals and meets the highest quality standards.

  • Drafting of study outlines and synopses
  • Creation of full study protocols
  • Development of patient-facing documents (informed consent forms & patient information sheets)
  • Writing of Clinical Study Reports (CSR)
  • Scientific writing for publications and congress posters
  • Preparation of study newsletters and updates for stakeholders
  • Alignment with ICH-GCP, regulatory requirements, and sponsor standards
Accuracy

Our writers combine medical expertise with linguistic clarity to ensure technically precise and scientifically sound documentation.

Compliance

All documents are prepared in line with current guidelines (ICH-GCP, EMA/FDA) and sponsor-specific templates.

Audience-Driven

Whether addressing patients, ethics committees, or scientific peers—we tailor tone and structure for maximum impact.

Collaboration

Working closely with biometrics, project management, and regulatory affairs ensures that content is consistent, timely, and aligned.

From Protocol to CSR – Consistency Across All Stages

  • Our medical writing process begins early—often with the study outline or synopsis—and extends through to the final Clinical Study Report. We ensure that the story of your study remains consistent, structured, and scientifically sound from start to finish.
  • By maintaining continuity across documents and aligning closely with biometric and clinical teams, we help sponsors present a cohesive and credible study narrative.

Turning regulations and research into readable results.

Writing for clinical studies isn’t just about text—it’s about balancing science, compliance, and readability. Here’s how we do it:

  • Clear, Purpose-Driven Documents: We create documents that do more than fulfill regulatory requirements—they guide, inform, and support decision-making throughout the study lifecycle.
  • Patient-Focused Communication: Informed consent and patient materials are crafted with clarity and empathy—ensuring accessibility while retaining accuracy.
  • Scientific Visibility: Our team supports scientific dissemination through the creation of congress posters, publications, and newsletters—ensuring your data reaches the right audience in the right format.

"We are collaborating with Alcedis for many years in several indications and as such in some local oncology studies. I believe one of the success factors for Alcedis is their high commitment and the hard work they bring into assigned projects. Besides great expertise in clinical research, another sweet spot is definitely their IT solutions for innovative data capture in clinical studies."

Dr. Lars Mühlenhoff
AstraZeneca, Director Medical Affairs Oncology

"I have made very good experiences with Alcedis in several global projects over the last years. I recommend their professionalism and hands-on mentality as a full service CRO with excellent eCRF solutions. Working with such a dedicated team was joyful on top and I can fully acknowledge Alcedis as a trusted partner!"

Alexey Medvedchikov
Boehringer Ingelheim, Regional Medical Affairs Operations

Latest Whitepaper

Our summarization of EUCROF's propositions on leveraging remote source data verification and reviews (rSDV/rSDR) in clinical trials. Gain insights and recommendations for seamless integration, ensuring data consistency and participant privacy while reducing site burden.

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