Basic info
Industry
writing and editing
Sectors
Biotechnology
Protocols
Regulatory Medical Writing
Clinical Development Plans
amendments
Medical Devices
Development Safety Update Reports
Study Design and Synopsis Writing
CSR and patient narratives
Pediatric Plans (PSP/PIP)
Briefing books
Investigational New Drugs
Integrated safety and efficacy summaries
Investigator brochures - new and updates
Integrated Solutions
CTD modules (mainly module 2)
ICFs
Clinical and pre-clinical manuscripts
Project Coordination
Professional Services
IMPD's
Clinical overviews
Medical
Biopharma
Quality Control Document
Life Science
Informed Consent Forms