Dover Brook Associates
Research, Po Box 177, Chester, New York, 10918, United States, 1-10 Employees
Phone Number: 84********
Who is DOVER BROOK ASSOCIATES
We are a recognized Process Authority with the FDA with over 28 years of experience and have assisted major food and pharmaceutical manufacturers and suppliers in engineering design and c...
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Headquarters: Po Box 177, Chester, New York, 10918, United States
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Date Founded: 1988
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Employees: 1-10
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Revenue: $1 Million to $5 Million
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Active Tech Stack: See technologies
Industry: Research
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Frequently Asked Questions Regarding Dover Brook Associates
Answer: Dover Brook Associates's headquarters are located at Po Box 177, Chester, New York, 10918, United States
Answer: Dover Brook Associates's phone number is 84********
Answer: Dover Brook Associates's official website is https://doverbrookassociates.com
Answer: Dover Brook Associates's revenue is $1 Million to $5 Million
Answer: Dover Brook Associates has 1-10 employees
Answer: Dover Brook Associates is in Research
Answer: Dover Brook Associates top competitors include: Manhattan Medical Research
Answer: Dover Brook Associates contact info: Phone number: 84******** Website: https://doverbrookassociates.com
Answer: We are a recognized Process Authority with the FDA with over 28 years of experience and have assisted major food and pharmaceutical manufacturers and suppliers in engineering design and compliance with FDA guidelines. Dover Brook Associates provides technical, regulatory and engineering support worldwide to the food and drug industries. We offer a wide range of services but our specialty is in the area of sterile processes, with an emphasis in aseptic processing/packaging and retort systems. Our project capabilities range from regulatory assistance, engineering design and support, thermal process development, microbiological testing, product development, contract packing assistance, and technical communication and training programs. Dover Brook Associates actively partners with manufacturers and employs its professional experience in assisting with the successful completion of major company projects, by not only obtaining USFDA low acid acceptance but also validating facilities worldwide.
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