Global Pharma R&D + Medical Writing & Designing

June 15, 2015 

The Assignment

Protocols, Patient Guidance and Data Collection Forms for highly specialized Pharmaceutical Clinical Research topics.

The Approach

For such a specialized R+D project, adherence to the International Regulatory requirements is key.

The Solution

Knowledge and Expertise in the European and American Regulatory Standards for Pharmaceutical Clinical Research are mandatory. The Medical team used its years of experience and expertise to select the appropriate formats, tools, and planning for designing the necessary Protocols, Patient Guidance, and Data Collection Forms. The Medical team invested time and resources in detailed background research to ensure the accuracy of the specialized Clinical Research content. Original and effective content was developed to meet the client requirements, within the specified timeline and budget limitations.