The success of a meticulously done research and tenaciously conducted clinical trial depends on a large extent to the well structured scientific & regulatory document presented to the regulatory authority.
Our expert team of medical writers can assist you at any point in your writing development life cycle. We have expertise in all the documentation you need.
At ScientiaBio, we strive to deliver actionable results to address your clinical trial need. Our quality review team continuously ensures the highest standard and compliance with style guides and regulatory guidelines throughout thousands of pages of documentation.
Our various types Medical writing services :
Regulatory Medical Writing
- Protocol development including synopses amendments
- Inform consent form
- Clinical Study Report
- SOPs
- Investigator Brochure
- Development of safety update report
- Periodic safety update report
- Periodic Adverse drug experience report
Scientific Medical Writing
- Primary and secondary manuscripts
- Review articles, Abstracts, Posters
Medico Marketing Materials