
Gemini Bio
Biotechnology, 920 Stillwater Rd, West Sacramento, California, 95605, United States, 51-200 Employees
Who is GEMINIBIO
Founded in 1985, GeminiBio serves the global biotechnology industry, from basic research to commercial production, with a focus on helping our customers accelerate the development of life...
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Headquarters: 920 Stillwater Rd, West Sacramento, California, 95605, United States
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Date Founded: 1985
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Employees: 51-200
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Revenue: $25 Million to $50 Million
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Active Tech Stack: See technologies
Industry: Biotechnology
SIC Code: 3568
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NAICS Code: 541720 |
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GeminiBio Org Chart and Mapping
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Frequently Asked Questions Regarding GeminiBio
Answer: GeminiBio's headquarters are located at 920 Stillwater Rd, West Sacramento, California, 95605, United States
Answer: GeminiBio's official website is https://gembio.com
Answer: GeminiBio's revenue is $25 Million to $50 Million
Answer: GeminiBio's SIC: 3568
Answer: GeminiBio's NAICS: 541720
Answer: GeminiBio has 51-200 employees
Answer: GeminiBio is in Biotechnology
Answer: GeminiBio contact info: Phone number: Website: https://gembio.com
Answer: Founded in 1985, GeminiBio serves the global biotechnology industry, from basic research to commercial production, with a focus on helping our customers accelerate the development of life-enhancing biotherapeutics. The company focuses on producing cell culture products and solutions that help customers streamline their discovery, development, and production processes, and by making catalog and custom cGMP bioprocess liquids that radically simplify customers' manufacturing workflows regardless of batch size. Located in West Sacramento, California, GeminiBio has two manufacturing facilities, comprising a total of 57,000 square feet. To meet the stringent needs of biotechnology research and production customers, the company's cell culture sera and bioprocess liquid manufacturing facilities are segregated between animal origin-free cGMP manufacturing and animal component cGMP manufacturing. GeminiBio is an ISO 13485 certified, FDA registered Class 1 Medical Device Manufacturer, aligned with 21 CFR Part 820.
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