SolutionsMedical Writing

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“IN ACHIEVING THE FINAL SUCCESSFUL GOAL, WE DO NOT SIMPLIFY THE SCIENCE, WE SIMPLIFY THE WRITING”

Accelsiors CRO has built a very potent team of medical writers with considerable experience in medical and regulatory writing services. Our medical writers are selected based on their scientific and medical expertise, combined with their clinical trials experience. Quality is enhanced by strict adherence to internal standard procedures and applicable guidelines. 

Here at Accelsiors, we understand that meeting quality standards and timelines is crucial; however, we take it one step further. We emphasize in clear planning, especially during the critical start-up phase of a project. We strive to meet interim timelines and to accomplish a proactive document development – our study report shell is developed well in advance of the study end, ensuring a maximum focus on study discussions and conclusions. Our approach for CSR preparation is foresighted, including as much preparatory work as possible, performed before the statistical analysis, to shorten the delivery timelines. Your interest and timelines are always the top priority for us.

Our processes ensure in-depth understanding by timely client review and feedback, quality by timely re-evaluating areas for improvement and consequently client confidence throughout the process. Our most important goal is to deliver the final product to you without last minute surprises and guarantee a trouble-free conduction of your study.

MEDICAL WRITING SERVICES:

  • Clinical study protocols
  • Clinical Study Reports (CSR)
  • Common Technical Document (CTD)
  • Integrated summaries of efficacy and safety
  • Briefing documents and scientific sections for regulatory documents
  • Safety reviews and narratives
  • Investigator brochures
  • Informed Consent Forms
  • Patient facing materials, layman summaries
  • Pediatric investigational plans (PIPs)
  • Journal articles, conference posters and presentations