Medical writing Services

IBCR has network of dynamic, presentable and approachable freelance medical writers with large experience in clinical trials execution. IBCR provides a full range of writing services for regulatory submissions, scientific communications and medico-marketing materials across diverse therapeutic areas for all phases of product life cycles, from pre-clinical development to post-marketing literature. We ensure timely delivery of accurate, consistent and regulatory compliant documents to our sponsors in a cost effective and flexible manner.

IBCR freelancers focus on

• The best time management
• Continuity and stability
• High productivity
• Cooperative
• Effective communication.

IBCR provides support medical writing services for the development phase such us:

• Clinical Protocols (BA/BE & Phase II to IV)
• Informed Consent Documents
• Annual Safety Reports
• Clinical Study Reports
• Patient Narratives
• Clinical Trial Registry Synopses
• Abstracts and Posters
• Manuscripts
• Remaining CTD Modules

In addition, IBCR with a broad spectrum of knowledge and specialist skills in specific indications can adapt to new projects in a short time with minimal assistance.

Peer Review and Quality Check Process:

At IBCR, each document goes through an extensive peer- and management review process. Before finalization, each document is reviewed by our medically qualified personnel from Medical Affairs Division. Document management is done under strict security measures to maintain data confidentiality. Documents are finalized after undergoing stringent quality control checks. All documents conform to ICH guidelines.

Our Freelance medical writers are able to work in accordance with client SOP’s to fasten the service deliverables.