Chroma Research Labs

Chroma Research Labs

Pharmaceuticals, 25 Health Sciences Dr, Stony Brook, New York, 11790, United States, 1-10 Employees

chromaresearchlabs.com

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Who is CHROMA RESEARCH LABS

Chroma Research Labs is an FDA registered cGMP/GLP facility located in Stony Brook, New York, that assists Pharmaceutical, Nutraceutical, and Cosmetic companies in developing and validati...

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  • 25 Health Sciences Dr, Stony Brook, New York, 11790, United States Headquarters: 25 Health Sciences Dr, Stony Brook, New York, 11790, United States
  • 2012 Date Founded: 2012
  • 1-10 Employees: 1-10
  • dollar-icon Revenue: Under $1 Million
  • tech-icon Active Tech Stack: See technologies

industries-icon Industry: Pharmaceuticals

SIC SIC Code: 8071

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Frequently Asked Questions Regarding Chroma Research Labs

Answer: Chroma Research Labs's headquarters are located at 25 Health Sciences Dr, Stony Brook, New York, 11790, United States

Answer: Chroma Research Labs's official website is https://chromaresearchlabs.com

Answer: Chroma Research Labs's revenue is Under $1 Million

Answer: Chroma Research Labs's SIC: 8071

Answer: Chroma Research Labs has 1-10 employees

Answer: Chroma Research Labs is in Pharmaceuticals

Answer: Chroma Research Labs contact info: Phone number: Website: https://chromaresearchlabs.com

Answer: Chroma Research Labs is an FDA registered cGMP/GLP facility located in Stony Brook, New York, that assists Pharmaceutical, Nutraceutical, and Cosmetic companies in developing and validating chromatographic test procedures, conducts routine lab testing as well as laboratory training. Our experienced lab personnel, along with the quality of their work, will drive the repeat business that we mainly rely upon. Professional services of Chroma Research Labs include: Development and validation of analytical procedures as per USP, ICH, FDA, and EMA guidelines. Heavy metals testing (Ca Prop-65) and minerals testing for dietary supplements, drug products and raw materials Analytical release testing of finished products and raw materails Accelerated stability study to support shelf life determination Dissolution profile comparison study (F1 and F2) Delayed release and sustained release testing GMP training, GMP audit, process validation and computer system validation Pharmaceutical laboratory training

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