Smithers - Pharmaceutical Development Services

Smithers Pharmaceutical Development Services

Pharmaceuticals, 11 Firstfield Rd, Gaithersburg, Maryland, 20878, United States, 51-200 Employees

smithers.com/industries/life-science/pharmaceutical/bioanalytical

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phone no Phone Number: 33********

Who is SMITHERS - PHARMACEUTICAL DEVELOPMENT SERVICES

Smithers PDS LLC (Pharmaceutical Development Services) assists in the development of new medicines by providing bioanalytical services for all phases of drug development from discovery th...

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  • 11 Firstfield Rd, Gaithersburg, Maryland, 20878, United States Headquarters: 11 Firstfield Rd, Gaithersburg, Maryland, 20878, United States
  • 51-200 Employees: 51-200
  • dollar-icon Revenue: $250 Million to $500 Million

industries-icon Industry: Pharmaceuticals

SIC SIC Code: 8071 | NAICS Code: 541715 | Show More

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Frequently Asked Questions Regarding Smithers - Pharmaceutical Development Services

Answer: Smithers - Pharmaceutical Development Services's headquarters are located at 11 Firstfield Rd, Gaithersburg, Maryland, 20878, United States

Answer: Smithers - Pharmaceutical Development Services's phone number is 33********

Answer: Smithers - Pharmaceutical Development Services's official website is https://smithers.com/industries/life-science/pharmaceutical/bioanalytical

Answer: Smithers - Pharmaceutical Development Services's revenue is $250 Million to $500 Million

Answer: Smithers - Pharmaceutical Development Services's SIC: 8071

Answer: Smithers - Pharmaceutical Development Services's NAICS: 541715

Answer: Smithers - Pharmaceutical Development Services has 51-200 employees

Answer: Smithers - Pharmaceutical Development Services is in Pharmaceuticals

Answer: Smithers - Pharmaceutical Development Services contact info: Phone number: 33******** Website: https://smithers.com/industries/life-science/pharmaceutical/bioanalytical

Answer: Smithers PDS LLC (Pharmaceutical Development Services) assists in the development of new medicines by providing bioanalytical services for all phases of drug development from discovery through approval and post market surveillance. We work with our customers to develop new methods, validate existing methods, as well as perform the assays necessary to analyze samples from patients on more than 100 clinical trials currently in different phases of the FDA regulated drug approval process. Our expert scientists perform large molecule bioanalysis, assay development, validation, and sample analysis at our GLP, GCP, and CLIA compliant laboratories.

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