BioClinAarc medical writing services are well organized to provide medical writing services for regulatory submissions, scientific communications and medico-marketing material across diverse therapeutic areas for all phases of product life cycles on a project-by-project or purposeful outsourcing basis.
Our experienced team of medical writers is responsible for producing comprehensive clinical study documentation that is fully compliant with ICH and GCP guidelines.
We offer a broad range of medical writing services, including:
Study protocols
Investigator brochures
Patient information leaflets
Informed consent documents
Operating procedures
Safety update reports
Regulatory dossiers
Medical publications
Interim and fully integrated final clinical study reports
This section of our website will enable you to learn more about becoming an BioClinAarc Investigator and also provides a dedicated resource centre for Investigators working with BioClinAarc Central Laboratories.
