Effective Medical Writing & Data Presentation
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| Date | Product | Location | Price | |
|---|---|---|---|---|
| No sessions are planned at this time, however if you are interested in taking this course click here | ||||
| If you would like to have this course as an in-house session click here | ||||
About this course
Reasons to attend
This Effective Medical Writing training provides you with basic skills of good medical writing. You will be able to write in a clear, consistent and concise way with specific attention for your audience, including reviewers, regulators, clinical staff, and their respective expectations.What's included?
- Documents and materials related to this course are included
- Globally recognised certificates awarded after test completion
- This course has been granted PharmaTrain Recognition
Course schedule
- Two Day face-to-face training: 09h00-17h00
Course Description
This Effective Medical Writing training is intended for medical doctors, pharmaceutical professionals, and researchers in the biomedical field who regularly need to write in English.The course provides practical guidelines that will help you improve your medical writing.Programme highlight
- Accurate vocabulary (avoiding ‘pharmaspeak’, ethically correct wording, accurate wording)
- How to guide the reader through the text
- The correct tense use in each section of the scientific article
- Reducing word count techniques
- Language enrichment
- Reviewing and editing of a document
- Information structure in publications and manuscripts (IMRAD)
- Designing and using tables and figures
- Typical language problems in scientific writing
Learning objectives
- Improve your writer skills and what techniques to apply in order to upgrade your writing to the expected standard
- Communicate in a clear and concise manner
Who should attend
Anyone who needs to write clinical trials documents as protocol, IB etc.
Competencies
This course covers competencies that are part of the ECCRT Competency Framework
- Scientific Concepts & Research Design (0)
- Ethical & Participants Safety Considerations (0)
- Investigational Product Development and Regulation (0)
- Clinical Studies Operations (GCPs or ISO 14155) (0)
- Study and Site Management (0)
- Data Management and Informatics (0)
- Leadership and Professionalism (0)
- Communication (2)
- Teamwork (0)
- Business acumen (0)
Trainers
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