Enco Pharmaceutical Development
Pharmaceuticals, 4810 Executive Park Ct, Jacksonville, Florida, 32216, United States, 1001-5000 Employees
Phone Number: +19*********
Who is ENCO PHARMACEUTICAL DEVELOPMENT
ENCO Pharmaceutical Development, Inc (EPDI) was acquired by Eurofins in the fall of 2022, and now exists as Eurofins BioPharma Product Testing ENCO, Inc. We continue to operate from our l...
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Headquarters: 4810 Executive Park Ct, Jacksonville, Florida, 32216, United States
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Date Founded: 2005
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Employees: 1001-5000
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Revenue: $1 Million to $5 Million
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Active Tech Stack: See technologies
Industry: Pharmaceuticals
SIC Code: 8731
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NAICS Code: 541714 |
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Frequently Asked Questions Regarding ENCO Pharmaceutical Development
Answer: ENCO Pharmaceutical Development's headquarters are located at 4810 Executive Park Ct, Jacksonville, Florida, 32216, United States
Answer: ENCO Pharmaceutical Development's phone number is +19*********
Answer: ENCO Pharmaceutical Development's official website is https://encopharma.com
Answer: ENCO Pharmaceutical Development's revenue is $1 Million to $5 Million
Answer: ENCO Pharmaceutical Development's SIC: 8731
Answer: ENCO Pharmaceutical Development's NAICS: 541714
Answer: ENCO Pharmaceutical Development has 1001-5000 employees
Answer: ENCO Pharmaceutical Development is in Pharmaceuticals
Answer: ENCO Pharmaceutical Development contact info: Phone number: +19********* Website: https://encopharma.com
Answer: ENCO Pharmaceutical Development, Inc (EPDI) was acquired by Eurofins in the fall of 2022, and now exists as Eurofins BioPharma Product Testing ENCO, Inc. We continue to operate from our locations in Jacksonville FL and Cary NC, and are excited to be part of the larger enterprise. Eurofins BioPharma Product Testing is the largest network of harmonized bio/pharmaceutical GMP product testing laboratories worldwide providing comprehensive laboratory services for the world's largest pharmaceutical, biopharmaceutical and medical device companies. Our comprehensive service offerings include testing of drug substance, final product, intermediates, and starting materials for both small and large molecule drug products. We offer a broad range of methodologies under GMP authorization, ISO 17025 accreditation and ISO 9000 certification and all analysis are performed according to European and British Pharmacopeia (EP and BP), United States Pharmacopeia (USP) and Japanese Pharmacopeia (JP), as well as specific customer methods. With a global capacity of more than 2 million square feet and facilities spanning 19 countries, our network of GMP laboratories operates under the same strict quality procedures, LIMS and centralized billing system across 37 locations worldwide.
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