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ENV Services, Inc., an ISO/IEC 17025:2017 accredited company strives to maintain and inspire professional excellence by providing Validation Services to our Pharmaceutical, Biotechnology and Medical Device customers.  We have the experience, expertise, and commitment to provide the superior service required to meet all of your validation and compliance needs.

We offer a full spectrum of services such as process validation, clean room certification, temperature mapping, process equipment qualification, pre-validation and calibration as well as startup. Dedication to quality, personalized support and the success of your projects are paramount for our success.



We are well-versed in the specific requirements of pharmaceutical and biotechnology compliance. We supply full cGMP documentation packages and offer periodic re-qualification to meet strict FDA standards. All of our validation services are thoroughly documented and are methodically reviewed by our quality assurance department before being released to the customer.

ENV support all areas of life science companies including manufacturing, packaging, facilities engineering, maintenance, microbiology, analytical research and development and quality control. 

Validation Services include:

  • Installation Qualification (IQ)

  • Operational Qualification (OQ)

  • Performance Qualification (PQ)

  • Summary Reports

  • Quality Control

  • Protocols

  • Temperature Mapping

  • Calibration

  • Certification of Clean Air Equipment (Bio-Safety Cabinets, Chemical Fume Hoods, Clean rooms and Environmental monitoring.

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