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EffiChem gives you confidence, not only in quality laboratory results and products, but in the data that you provide to auditors, accreditation, and inspectors.

Complicated Processes Become Simple


GAMP compliance

EffiChem software is designed and developed in accordance with GAMP 5 guidance. EffiChem ensures the proper documentation and execution of all validation activities, specifically the Specifications and Testing components of GAMP 5 so that your lab’s computer systems create as little risk as possible.

See the GAMP website

21 CFR Part 11 Compliance

EffiChem software is a closed system, with all 21 CFR Part 11 requirements accounted for, including limited system access, electronic audit trail, accurate copies, and accurate retrieval. You stay compliant with all current industry trends focused on data integrity and traceability.

See the FDA website

ISO 17025 Technical Requirements

EffiValidation was designed to not only reduce time, but improve quality and efficiency by taking the ambiguity out of method validation, while ensuring that data integrity is protected, and results are available at the click of a mouse. This means that you can save up to 60% more time when using EffiValidation.

See the ISO 17025 website

ISO 17025 Management Requirements

EffiQS covers the whole laboratory process, enabling you to manage every relevant aspect of your quality process from one place, and keep authenticated records that help you maintain ISO 17025 accreditation, GMP standards, and 21 CFR Part 11 compliant records.

See the ISO 17025 website

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