GC Qualification Process
The gas chromatography qualification service package with various detectors is as follows:
Gas Chromatography (GC) Qualification Services
Gas Chromatography (GC) is an advanced analytical method for volatile organic compounds, offering excellent performance in separating and identifying each compound within a matrix.
In the pharmaceutical industry, GC systems are regarded as core instruments in Quality Control (QC) laboratories. Regulatory inspection bodies impose strict requirements for verifying operational accuracy and implementing intermediate checks. Pharmaceutical companies, QC laboratories, and other related facilities are required to perform qualification of their instruments at defined intervals.
Our company provides a complete package of GC qualification services in accordance with EDQM, USP, and other relevant guidelines and protocols. These services include:
- Pre‑assessment – Reviewing existing documentation, identifying requirements, and providing free consultation.
- Installation Qualification (IQ) – Preparing protocols and completing documentation to verify correct installation.
- Operational Qualification (OQ) – Preparing protocols, performing tests, and documenting verification of correct system function.
- Performance Qualification (PQ) – Preparing protocols, performing tests, and documenting verification of analytical performance under real operating conditions.
Our expert team delivers these services for all major GC brands and a wide range of detectors, including Mass, MS/MS, FID, TCD, and more
