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Biopharmax Group

Biopharmax Group

Biotechnology, Waldorf, Maryland, 20602, United States, 51-200 Employees

biopharmax.com

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Who is BIOPHARMAX GROUP

Biopharmax is a leading international design and construction company of Pharmaceutical, Biotechnological and Chemical (API) plants including critical, sterile systems and clean rooms. Bi...

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  • Waldorf, Maryland, 20602, United States Headquarters: Waldorf, Maryland, 20602, United States
  • 51-200 Employees: 51-200
  • dollar-icon Revenue: $25 Million to $50 Million
  • Sarel Tov CEO:   Sarel Tov

industries-icon Industry: Biotechnology

SIC SIC Code: 8731

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Biopharmax Group Org Chart and Mapping

Sarel Tov

Sarel Tov

CEO

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Frequently Asked Questions Regarding Biopharmax Group

Answer: Biopharmax Group's headquarters are located at Waldorf, Maryland, 20602, United States

Answer: Biopharmax Group's phone number is +35*********

Answer: Biopharmax Group's official website is https://biopharmax.com

Answer: Biopharmax Group's revenue is $25 Million to $50 Million

Answer: Biopharmax Group's SIC: 8731

Answer: Biopharmax Group has 51-200 employees

Answer: Biopharmax Group is in Biotechnology

Answer: Biopharmax Group contact info: Phone number: +35********* Website: https://biopharmax.com

Answer: Biopharmax is a leading international design and construction company of Pharmaceutical, Biotechnological and Chemical (API) plants including critical, sterile systems and clean rooms. Biopharmax has 40 years of experience. Biopharmax specializes in execution of projects for the Pharmaceutical and Biotechnological industries on a "turnkey" basis. Based on its multi-disciplinary experience and unmatched in-house flexibility,Biopharmax offers a wide range of engineering specialties to suit the requirements of its customers and partners worldwide. Serving its customers from A to Z, Biopharmax undertakes all project management, design, construction, commissioning and validation until the hand-over of a complete plant. Biopharmax is committed to: # Maintain the highest engineering standards to achieve cGMP as required by the various authorities (e.g. FDA, EMEA, etc). # Execute the project precisely so that schedule and cost estimations are accomplished, without compromising on quality or performance.

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