Medical Writing
Bioforum CDmC offers senior professionals in clinical trials assistance in writing, editing and translating of all documents needed for clinical trials.
Our experts provide a combination of academic knowledge and professional writing skills, which is a guarantee for high quality and cost effectiveness.
This department is headed by Dr. Eldar, who has established and managed the Medical Knowledge Center of the Regulatory Affairs and Clinical Trials departments in Bristol-Myers Squibb (BMS), a leading international pharmaceutical company.
Key services:
- Preparation / translations / back translations of:
- Informed consent forms, adjusted to MOH format
- Protocols
- Medical based answers to physicians and pharmacists
- Safety information
- Back translations
- Medical information
- Literature review
For more information please click here
|