CONTRACT FORMULATION DEVELOPMENT, MANUFACTURING AND ANALYTICAL SERVICES

September 3, 2020 By rperez

Formulation, development, testing and manufacturing of pharmaceutical products. Our services are cGMP compliant and include established protocols, efficient documentation practices, and effective QA management. We can be your greatest resource. Contact us at (904) 645-9169.

ISO/IEC 17025 is a company level accreditation based on a standard published by the International Organization for Standardization (ISO) titled “General requirements for the competence of testing and calibration laboratories”. ISO/IEC 17025 is a general umbrella term used to refer to the specific standard; the current version of this standard is ISO/IEC 17025:2017. The standard contains two main sections: management requirements (primarily related to the operation and effectiveness of the quality management system within the laboratory) and technical requirements (primarily related to the competence of staff and calibration of equipment). The standard also gives requirements related to quality management such as document control and corrective action. This standard is the basis for accreditation from an accrediting body.

ADPEN has also been inspected by the US-EPA and US-FDA multiple times with no observations.

CONTRACT FORMULATION DEVELOPMENT, MANUFACTURING AND ANALYTICAL SERVICES

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