Medical and Technical Writing

Archemin understands the scope of medical writing

In a specialist business like ours, there is so much information you can get on the Internet that you often spend huge amounts of time looking for. Our medical writing service here complements other online services by providing a valuable opportunity for you to save time and money and get on with what's important.

We keep up with relevant scientific literature, current developments and business directions within the medical and pharmaceutical industries. Therefore, Archemin manages medical writing activities so that timelines and budgets are met!

We provide medical and technical writing services in support of regulatory submissions, clinical trials and other scientific documents.

Regulatory Affairs documents

  • Summary of Product Characteristics, Patient Information Leaflets
  • Periodic Benefit-Risk Evaluation Report (PBRER)
  • Summaries and overviews of Clinical and Preclinical data
  • Chemical-Pharmaceutical data

Pharmacovigilance documents

  • Pharmacovigilance procedures
  • Risk Management Systems & Risk Management Plans
  • Periodic Benefit-Risk Evaluation Report (PBRER)

Clinical Trial Documents

  • Protocols (all phases)
  • CRF design / remote data capture systems
  • Investigator Brochures
  • Diary cards
  • Informed consent leaflets and Patient information sheets
  • Trial reports

Scientific Documents

  • Publications, abstracts, posters, full manuscripts
  • Scientific argumentation
  • Reports of Delphi-panel meetings

You name it, we write it !

Want to know more / require a quote ?

Send your request to mw [at]