A well written document can ease the review path for regulators and development partners, reducing risk and maximising opportunities.
A well written document can ease the review path for regulators and development partners, reducing risk and maximising opportunities.
Our flexible and adaptable medical writing team is highly experienced in both regulatory clinical writing and medical communications and offer support from Briefing Books to Licensing, Protocol Synopsis and Protocols to CSRs and Lay Summaries, from Manuscript to Publication and everything in between.
The whole team have in depth knowledge and understanding of both European and US guidelines and are acutely aware of our audience – be it Regulatory Agencies, Investigators or members of the public.
We can provide medical writing consulting services and support as either stand alone, as part of a transcrip team working with the client or embedded within a client’s team.
We have teams of life science and R&D experts to help achieve your goals and seize opportunities. Whatever your project requires, we have the people to meet your needs.
