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Medical Writing:
I offer services in writing, editing,
quality control and review of the following clinical research documents:
- Protocols and protocol amendments
- Investigator brochures (IBs) and IB updates
- Clinical study reports
- Patient narratives
- Standard operating procedures (SOPs) and SOP
templates
- Medical education (abstracts, papers for journals,
scientific slide kits)
- Newsletters
I can also prepare the following pharmaceutical
business publications:
- Market intelligence reports
- Business articles
Medical Translations:
As a native Portuguese speaker, I
can offer translations from English to Portuguese of all clinical
study-related documents for trials performed in Brazil.
Scientific Training:
I can offer training in pharmacogenomics.
This training takes the form of a workshop that gives participants
an understanding of how drug response is affected by inherited differences,
and how this knowledge is applied to drug development. Implications
for clinical trials, such as ethics and regulations are also covered.
The workshop can be delivered to either individuals or groups.
Regulatory Advice:
As a Brazilian, I can offer regulatory
support and guidance from start-up to close-out for clinical trials
performed in Brazil.
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