Scientific Writing Services
Our team of experienced clinical research experts will generate a broad range of documents related to the clinical trial design and management in compliance with the highest scientific and ethical standards. Our Scientific writing services include preparation of:
- Study Protocols and revision
- Case Report Forms
- Investigator Brochures
- Participant advertisement
- Participant information sheet and Informed Consent Forms
- Data Management plans
- Recruitment plan
- Case report form completion guidelines (CRF-CG)
- Trial Monitoring Plan
- Clinical Study Reports
- Abstract and Manuscripts
- Poster presentations
- Customized reports