• Regulatory writing for clinical research industry
• Medical literature search
• Power point slides and training modules
• Patient education
• Editing strategies
• Sanet has an advanced degree in medical science (PhD) and will accurately write about your topic.
• She has experience in writing in a wide variety of documents in different therapeutic areas (eg clinical research protocols, Informed consent, expert reports, clinical investigational reports, clinical evaluation reports for medical device , training slides/modules, presentation slides at congresses, editing/reviewing documents, manuscripts for scientific journals, regulatory submissions).
• You can rely on her writing skills and providing documents as per your deadline.
Previously served Medical Non- Profits, Biotech, Vaccine, Pharma and Medical Device Companies.
Contact Dr Aspinall at email@example.com to discuss your medical writing project and obtain a cost estimate.