IICRM provides a team of expertise medical professionals for medical writing services to our clients. Our team for medical writing is proficient with essential skills, capability and approach to provide high quality clinical study documents compliant with ICH guidelines and regulatory requirements.
Medical writing plays a crucial role in each level or division of clinical trial study development, right from the beginning level of notional molecule to conclusive stage. Our aim is to provide superior quality with in time limit for clients.
Medical Writing includes the following services:
- Clinical trial protocols
- Investigator’s Brochure
- Study assessment questionnaires
- Informed consent form
- Patient information sheet
- Patient dairies
- Clinical overview and clinical summary
- DSMB manuals
- Abstracts and manuscripts
- Clinical study reports (as per ICH-E3)
- Medical manuscripts and abstracts