Medical writing
Medical writing is established in pharmaceutical industry, because it requires special skill to produce well-structured documents hat present information clearly and concisely. Medical writing for pharmaceutical industry can be classified as either regulatory medical writing or educational medical writing. Regulatory medical writing means creating the documentation that regulatory, which include clinical protocols, clinical study reports, patients informed consent forms, investigator broachers and summary documents.
Educational medical writings mean writing documents about drugs, devices and biologics for healthcare professionals. These contain sales literature for newly launched drugs and data presentations at conferences.
Related Conference of Medical writing
Medical writing Conference Speakers
Recommended Sessions
- Advances in medical imaging
- Artificial Intelligence
- Cardiac imaging
- Case report on clinical research
- Clinical biostatistics and data management
- Clinical research
- Clinical Trails
- Clinical trial on cardiology
- Clinical trial phases
- Computed tomography
- Magnetic resonance imaging
- Medical Imaging
- Medical Physics
- Medical writing
- Molecular Imaging
- Neuroimaging
- Nuclear Medicine
- Oncology
- Ophthalmology Diagnosis
- Pathology imaging
- Pre-Clinical Research
- Radiation Oncology
- Radiation therapy
- Radiography
- Ultrasonography
- Uses of medical imaging