Our Services
From discovery to approval, we help you transform your innovative ideas into reality with our comprehensive suite of services tailored to guide you through every stage of the process.
Create. Collaborate. Achieve.
We offer a comprehensive suite of services designed to guide you through every stage of product discovery and development. Our expertise spans strategic planning and regulatory affairs, ensuring that your project meets essential standards while navigating complex landscapes. We specialize in early development and clinical trials, leveraging cutting-edge bioinformatics to enhance data analysis and decision making. With a robust approach to pharmacovigilance, we prioritize patient safety and compliance, complemented by our scientific and medical writing services that articulate your findings with clarity and precision. Additionally, our library services provide you with invaluable resources, and our eCTD services simplify regulatory submissions, empowering your journey from discovery to successful approval.
Our Services
Product Development Strategy
CCSA has a strong record of providing consulting services on strategies for drug development.
Regulatory Affairs
Discovery & Early Development
Board-certified toxicologists, pharmacologists, chemists, biochemists, microbiologists, nutritionists, and other scientists with extensive experience in nonclinical research and development make it possible to meet project timelines and goals.
Clinical Trials
CCSA’s clinical trial monitoring teams provide reliable expertise, exceeding our sponsors’ study timelines and high data quality standards.
Pharmacovigilance
Scientific & Medical Writing
Our scientists and medical writers bring extensive scientific research, writing, and editing skills to preparing materials in support of client programs.
eCTD
eCTD is the electronic transfer of information to regulatory agencies based on the Common Technical Document (CTD) format. eCTD utilizes PDF documents linked via an XML backbone.