At SDS Clinical Trials, our specialty is providing sponsors and CROs with rapid study enrollment, high subject etention, meticulous data and meeting critical timelines. By utilizing a central IRB combined with our 100,000+ patient database, our energetic and experienced, bi-lingual staff ensures SDS Clinical Trials will meet and exceed goals efficiently. SDS Clinical Trials' commitment to clinical research ensures patient safety, quality, and efficiency. The diversity among our experienced team provides great benefit to the research community. With more than 20 years experience, our Principal and Sub-Investigators are Board Certified in a wide range of therapeutic areas and are dedicated to treating study patients with the utmost dignity and compassionate care. Our highly motivated research team has outstanding ethics and values putting patient safety first. Our experienced staff is knowledgeable and strictly follows the FDA regulations, ICH/GCP guidelines, IRB standards, HIPAA and Sponsor requirements.