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 Safety Update Reports
- Summaries and overviews of Clinical and Preclinical data
- Chemical-Pharmaceutical data
- Pharmacovigilance procedures
- Risk Management Systems & Risk Management Plans
- Periodic Safety Update reports
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
- 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] archemin.eu