PharmEng Technology is a fully integrated consulting firm serving the Biotechnology and Pharmaceutical industry.
We are cGMP compliant leaders in providing services in commissioning and qualification, validation, quality systems, regulatory affairs, engineering, auditing, process development, technology transfer, and training.
We have hands on experience in handling FDA 483 warning letters, FDA Consent Decree, product recalls, compliance issues, manufacturing defects, out of specifications and non-conformances. PharmEng is a global compliance consulting firm with projects around the world. We will work with you to balance the needs of an ever-stringent regulatory environment which meets your business needs.
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