Our medical writers are qualified scientists with PhD degree in the biomedical sciences with experience from the pharmaceutical industry, Clinical Research Organizations (CROs) and academia. Therefore, Biomapas medical writing team fully support clients with the preparation of documents required for clinical research, regulatory affairs or scientific purposes, such as:
- Clinical Development Plans;
- Clinical Study Protocols;
- Investigator Brochures (IBs) and annual updates;
- Case Report Forms (CRFs);
- Informed Consent Forms (ICFs);
- ICH GCP compliant Clinical Study Reports (CSRs), including CSR synopses for public disclosure;
- Abstracts, manuscripts and journal articles;
- Medical and scientific literature reviews.
For any inquiry regarding our services, please contact Biomapas Business Development team.