Aspire Scientific

High-quality medical and regulatory writing is an essential part of any successful drug development program. With a wealth of knowledge and technical expertise, we develop a range of clinical trial and regulatory documents for our clients, including:

Clinical study protocols
Clinical study reports
Informed consent forms
Patient information leaflets
Lay summaries
CTD modules*

*Common technical document modules, focusing on clinical summaries (sections 2.7.3 and 2.7.4).

 

For further information about how Aspire Scientific can help you with your clinical trial and regulatory documentation, please contact Ryan Woodrow