Regulatory writing

Smartsource your clinical research documentation without having to worry about integrating the final output with your in-house styles and processes. Avoid delays in drug development by reducing the time you spend on fixing inappropriate/improper documentation. Our regulatory writers have a thorough understanding of regulatory processes and guidelines and will be able to work with your templates, systems, and processes, and within your time schedules and budget. They also have experience across a wide range of therapeutic areas. Working with Cactus Medical will result in cost benefits as well as benefits of scope and time.

Our clinical research documentation services include but are not limited to the following document types:

• Protocols
• Investigators’ brochures
• Case report forms
• Clinical study reports
• Clinical study synopsis
• Informed consent documents
• Periodic safety update reports
• Patient Narratives
• CTDs