SDS Clinical Trials

Sds Clinical Trials

Pharmaceuticals, 756 W Town and Country Rd, Orange, California, 92868, United States, 11-50 Employees

sdsclinicaltrials.com

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Who is SDS CLINICAL TRIALS

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 cen...

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  • 756 W Town and Country Rd, Orange, California, 92868, United States Headquarters: 756 W Town and Country Rd, Orange, California, 92868, United States
  • 2008 Date Founded: 2008
  • 11-50 Employees: 11-50
  • dollar-icon Revenue: $5 Million to $10 Million
  • tech-icon Active Tech Stack: See technologies

industries-icon Industry: Pharmaceuticals

SIC SIC Code: 8731 | NAICS Code: 541720 | Show More

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Frequently Asked Questions Regarding SDS Clinical Trials

Answer: SDS Clinical Trials's headquarters are located at 756 W Town and Country Rd, Orange, California, 92868, United States

Answer: SDS Clinical Trials's phone number is +17*********

Answer: SDS Clinical Trials's official website is https://sdsclinicaltrials.com

Answer: SDS Clinical Trials's revenue is $5 Million to $10 Million

Answer: SDS Clinical Trials's SIC: 8731

Answer: SDS Clinical Trials's NAICS: 541720

Answer: SDS Clinical Trials has 11-50 employees

Answer: SDS Clinical Trials is in Pharmaceuticals

Answer: SDS Clinical Trials contact info: Phone number: +17********* Website: https://sdsclinicaltrials.com

Answer: 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.

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