IQ/OQ/PQ Validation
IQ/OQ/PQ validation, executed by our engineers
Qualification of your new instrument, done on site by Pharma Biotech engineers, with documentation your QA team can approve.
What each stage covers
- Installation Qualification (IQ) — the instrument is installed as specified: delivery checks, location, utilities, software and documents.
- Operational Qualification (OQ) — the instrument works as intended across its operating range.
- Performance Qualification (PQ) — the instrument performs reliably in your routine use, with your samples.
How we work
- 1ProtocolFrom principal or Pharma Biotech
- 2ApproveYour QA signs off
- 3ExecuteOur engineers on site
- 4ReportSigned for your file
- Protocols come from the principal or are prepared by Pharma Biotech.
- Your QA reviews and approves the protocols.
- Our engineers execute the tests in your lab.
- We deliver signed reports for your validation file.
Systems we qualify
- Microbs IAN — including support for method validation against your compendial method
- Autobio Autof MALDI-TOF
- Lab equipment from our principals
Where
Across Bangladesh; our engineers travel to your site.
FAQ
Who writes the protocols?
The principal or Pharma Biotech; execution is always by our engineers.
Can you qualify equipment we bought elsewhere?
Ask us with the make and model, and we will tell you whether we can support it.
Tell us what your lab needs
An engineer replies with a recommendation and a quote.