I provide authoring services across the regulatory
medical writing spectrum for Phase I to IV clinical trials,
including:
[SOP, standard operating
procedure; CSR, clinical study report; PSUR, period safety update
report; IB, Investigators brochure]
I welcome requests to prepare ‘bespoke’
reports and am happy to discuss individual requirements. I will
work with you to ensure timely delivery of a quality
product prepared in a cost-effective manner.
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