SERVICES
  
 

Capabilities

  
  Expertise  
  Clients  
     

Capabilities

 

PUBLICATIONS, WEB, AND MEDICAL EDUCATION SUPPORT
(non-regulatory documents)

All documents and materials are constructed from fact-based sources:

MEDIA FOR PUBLICATION OR PRESENTATION
Abstracts, posters, monographs,  PowerPoint slide sets with supporting text and cited literature.
MEETING COVERAGE & PREPARATION OF ENDURING MATERIALS
On-site coverage of regional and national meetings, symposia, roundtables, or consensus forums; summary of proceedings; dissemination of meeting content for enduring publications; follow-up contact with presenters for content validation and updates of review articles, monographs, compendia of case studies, etc.
WEB-BASED PROJECTS
In-depth, personal assistance with content, flow, and accuracy for your company’s or institution’s website; consulting and placement of online material per target audience; help with content planning for your interactive educational forum in the life sciences or multimedia patient education project.
EDITING, ANALYSES & SUMMARIES
Quality control checks (including fact-checking for scientific accuracy of cited data sets, proper usage of biomedical terminology, and correct citation of literature); comprehensive literature searches with cited references; literature analyses; “white papers”; summaries of breakthrough technologies; historical overviews of medical specialty areas; editing for US researchers and clinicians, including international researchers whose primary language is not English.
INTERVIEWS
In-depth discussion and opinions from physicians and scientists on hot topics and clinical advances (these can be in a question and answer or other format for your monograph series, newsletter focus articles, etc.)
PATIENT EDUCATION
Preparation of content for brochures or other media for patient education, summarizing disease-specific or public health information (such as mode of disease transmission, prevention; diagnosis, signs/symptoms, treatment, etc.)

DRUG DEVELOPMENT - DOCUMENT PREPARATION
(FDA regulatory documents)

  • CSRs (Clinical Study Reports) - specializing in Phase 2 and Phase 3
  • Safety and efficacy summaries for NDA (New Drug Application)
  • Import of clinical & laboratory data into tables and graphic formats
  • QC fact-checking for accuracy of data sets and usage
  • Subject narratives