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Medical Writing Services

With the expertise and extensive experience, Omega CRO provides medical writing service, as a whole or at any stage of the writing process such as:

  • Protocol design

  • Case Report Form design

  • Informed Consent design

  • Writing final study reports

  • Preparing scientific publications about the study results

  • Research Design/Synopsis Writing

  • Research Protocol Writing

  • Research/Questionnaire Design

  • Informed Consent Form

  • Study Interim/Final Report Writing

  • Research/Questionnaire Form, Informed Consent Form Printing

  • Manuscript Writing

  • Manuscript Review in terms of Presentation

  • Manuscript Review in terms of Scientific Content

  • Manuscript Review in terms of Language/(Grammar)

  • Manuscript Review in terms of Journal Instructions

  • Manuscript Revision towards View of Journal Editor and Suggestions of Reviewers

  • Manuscript Translation

  • Abstract (Bulletin Summary) Preparation

  • Abstract/Manuscript Submission

  • Slide Preparation

  • Poster Preparation/Printing

  • Systemic Literature Searching

  • Manuscript Review in terms of Statistical Analysis

  • Statistical Analysis Report Interpretation

a) Trial Design Consultancy

This activity will aim to assist our sponsors by providing consultancy work in designing any research or service protocol. The consultant will help identify the most efficient design, most appropriate statistical analysis or other evaluation method and identify the outline to be followed so as to carry out the research in the most standardized manner.

b) Sample Size Consultancy

This activity will help applicants to come up with the optimal number of subjects that need to be enrolled to answer the primary research question at hand or to obtain the targeted magnitude of an intervention in a program.

c) Randomization Assistance

For any study that will perform at least two different approaches, the randomization assistance will provide an efficient randomization algorithm, prepare and distribute the lists or other randomization materials.

d) Ethical Review

This branch will oversee ethical problems that may be associated with any research or other program involving an intervention on subjects and make necessary adjustment to overcome these issues. If necessary, the branch will aid in preparation of necessary documents that will be used for Ethics Committee approval application.