Post-market Documents Creation
We provide full support for the creation and revision of attachments and interview forms.
With abundant resources and extensive expertise, we offer high-quality documents.
- We create documents based in the experience we have accumulated supporting the entire process, from clinical trials to post-market surveillance
- We assign staff with a background in pharmaceuticals.
- We offer procedures and schedules that meet your needs.
- We provide evidence-based manuscripts based on the characteristics of the drug and disease.
Excellent Human Resources
- We actively recruit highly capable personnel and train them based on our unique professional education program.
- Attachments (revision work compliant to the new guidelines for attachments is also available)
- Medication Guides for patients.
- Interview forms
- Post-marketing surveillance reports
- Drug Information Sheet, etc.
- Manuscript creation (new creation and revisions)
- Quality Control
- Uploading data to authorities` websites, etc.