*Medical Affairs

Honorem understands that as clinical research is becoming increasingly complex, the development of clinical trial protocols is vital to conducting an effective study.

Our team of highly qualified MDs and Statistics PhD professionals will assist you in professional medical writing, coordination, and evaluation of clinical trials. Honorem’s statisticians, Clinical Operation Team and Data Management Team work synergistically together along with our medical writers. The team provides in-depth consultation and help document all stages of the product and research development.

Honorem medical affairs provides support in all aspects including regulatory, clinical development, pharmacovigilance, and post-approval programs. Our medical experts help guide our partners in navigating whatever obstacles and challenges that may arise.

•Medical Writing
  • - Protocol Writing / Synopsis Writing
  • - Translation Service
  • - Medical Administration
  • - Patient narratives
  • - Consulting for Clinical Study Design
  • - Concept Development
  • - Protocol/ICF Development
  • - Protocol/ICF/CRF Review
  • - CSR writing and Review
  • - Protocol Meeting with Investigator or Client
  • - CTD Preparation
•Regulatory Writing
  • - Advisory committee presentations
  • - Annual reports
  • - Briefing books
  • - Package inserts
•Scientific Writing
  • - Abstracts
  • - Advisory board presentations
  • - Posters
  • - Manuscripts
  • - Conference presentations
  • - Literature-based research