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IQ/OQ Validation Services
FromEsco Pharma
A certified process ensures that internationally compliant equipment is used pursuant to validated Standard Operating Procedures (SOPs).
Those SOPs that are applicable to equipment and instruments are classified as follows:
- Installation Qualification (IQ)?documents specify the receipt and proper installation of an equipment in a suitable environment.
- IQ is required for equipment installation, relocation, reconnection to modified sytems, and when established SOPs are changed.
- IQ can be performed by the customer or Esco.
- Operational Qualification (OQ) document proves that the equipment meets the correct specifications after installation.
- OQ can be performed by either Esco itself or the client, and it must be done annually.
Esco provides instructions for each product’s IQ and OQ procedures. Our team of specialized engineers can perform these services directly on behalf of the customers, or arrange them with independent approved local certifiers. The availability may vary from country to country and region to region. Also, Esco can train customer employees to perform IQ/OQ.
