Contract Medical Writing Services

OnPoint medical writing professionals provide high-quality regulatory and industry writing services for major international pharmaceutical, biotech, medical device and CRO companies. Each of our writers have demonstrated expertise in preparing regulatory-compliant submissions and industry-focused documents and presentations.

OnPoint writers are goal-oriented, resourceful professionals with proven experience in the development, writing, preparation, and management of pharmaceutical, regulatory, and industry documents and presentations. Our writers are able to work both independently and in diverse team environments, effectively managing and communicating with a broad range of individuals and target audiences.

OnPoint medical writers have an average of 10 years of industry experience in all phases of clinical research. Approximately 80% of our professionals hold advanced degrees. Some hold memberships and certifications from nationally recognized organizations such as BELS and AMWA. This level of preparation and professionalism ensures your projects are completed accurately, appropriately, and within budget.

OnPoint Medical Writing Areas of Strength

  • Effective project management with the ability to handle multiple projects simultaneously
  • Providing subject-matter expertise to support project implementation and completion
  • Interfacing and collaborating within diverse team environments
  • Ability to meet the demands in fast-paced environments that have changing priorities

 

OnPoint Medical Writing Specialities

Global Drug Development
(All phases)

 
 
 
 
 
 
 
 
Industry Documents and Presentations
 
 
 
Main Therapeutic Areas
Protocols and amendments
Investigator brochure
Informed consent/assent
Clinical study report
Benefit-Risk portfolios
Safety narratives
IMPD documents
Briefing documents
 
 
Benefit/ profiles
Abstracts
Slides
Education materials
 
Neurology/Neuroscience
Oncology
Respiratory
CTD/IND/NDA compilations
Briefing documents
Integrated summaries of safety/efficacy
Literature summaries
IMPD documents
Editorial/Quality Control review
Annual reports
Template preparation/editing
 
Risk management plans
Manuscripts
Posters
Grant applications
 
Endocrine/Metabolic
Cardiovascular
Infectious Diseases