I am primarily a regulatory medical writer, and I specialise in the following documents:

  • Clinical study reports (all phases)
  • Protocols (all phases)
  • Investigator brochures
  • Regulatory submission documents (CTD modules)

All documents are prepared to ICH standard.

I work to your own standard operating procedures (SOPs), and I will use your own document templates and style guides.

If you require, I can work within your company’s document management system. I am experienced in checking documents in and out, as well as following specified authoring and review processes.

I offer training for junior medical writers. This can be tailored to your requirements.

I always seek positive feedback on my services. Please visit the Testimonials page to read some of the comments.