At LLX, we are dedicated to providing clinical research services at home and abroad for bio/pharmaceutical and medical device industries. Our teams have proven expertise and reputation in supporting global clinical trials of different phases across various therapeutic areas for companies of various sizes in the United States and globally. We are committed to provide our clients with the highest quality and timely deliverables. Please look at the company profile for details.
- Biostatistics and Programming (Submission-ready statistical analysis)
- Data Management
- CDISC Implementation (SDTM/ADaM datasets and documents, Define.xml and submission)
- Consulting and Staffing Services
LLX services and systems are governed by well defined SOPs, policies and are compliant with regulatory requirements such as ICH/GCP, FDA 21 CFR Part 11 and other client specific standards to ensure compliance with the protocol, SOPs, and regulatory requirements as well as the integrity and validity of study data and programs for statistical outputs.
Your satisfaction is our mission. We are committed to advancing the most efficient and cost-effective path to the needs of our clients, and working for the best interests of our clients, employees, and communities. Our dedicated team serves as an extension of your team. We engage quickly and provide strategic thinking, deliver additional input, insight, and efficiencies to every step of our solutions.
Your success is our passion.