Medical Writing Services

medical writing services

Medical Writing

One of the specialities biosphere has is in Medical content writing!!!

Be it academic writing, regulatory writing, clinical writing or medical writing for specific projects, our medical writing services can plan and deliver the content as required. Our writing team works in co-ordination with our pharmacovigilance team, QA team, data management team and other team’s part of a project to create the necessary documentation for clinical trial projects.

We provide well-written documentation for your product development efforts by delivering high-quality services globally. Our qualified team of writers and editors has vast experience in managing medical content. With their expertise, Biosphere helps you to compile, organize, write, edit, and produce a wide range of medical scientific documents.

Based on the document needs of our clients, we create documents that demonstrate excellent language usage, clear communication and adherence to scientific writing standards. We provide cost-effective clinical writing consultation services for projects of various scope and scale. You can rely on us to maintain your superior quality and regulatory standards through our clinical writing services in globally.

Service Offered

  • Clinical sections of common technical documents (CTDs)
  • Clinical sections of new drug applications (NDAs)
  • Investigator’s brochure
  • Protocol writing
  • Informed consent form drafting
  • Documents pertaining to execution of clinical trial like patient diaries, templates for documentation etc.
  • Periodic safety update reports (PSURs) and other Pharmacovigilance documents
  • Clinical study reports

Benefits of hiring a clinical writing agency

  • Clarity in presentation of facts and figures can be found in our carefully articulated documents.
  • Analysis of substantial medical data requires expertise that Biosphere is equipped with.
  • Timely turnaround of high-quality documents improves the progress of the trial.

Speak to a member of our team about our clinical and safety data services

Our expert will work with you to gain insight to your molecule, anticipated outcomes and definite trial requirements and provide a customised design best suited for your molecule.

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