Creation of Validation Documents including Certificates and Inspection Reports
Confirmation and Certification of Equipment Requirements in the Pharmaceutical Industry
We are able to provide various certificates and inspection reports as validation documents as needed. We offer high-quality containers that can be used with confidence.
Quality Inspection Records and Validation
To verify the acceptance or rejection of the product, we create quality inspection records along with quality inspection reports and perform validation to ensure its validity. Based on the results of these quality inspection records, we determine the suitability for shipment.
– Steel Material Inspection Certificate (Mill Sheet)
– Electrolytic Polishing Certificate
– Inspection Certificate (Standard)
We can modify the template and content of these documents according to your requirements and requests.
What is “Validation”?
Validation is the process of verifying that the expected results can be achieved based on the structure, procedures, processes, and other manufacturing and quality control methods of a manufacturing facility, and documenting the results. Validation is also known as confirmation of suitability and involves the following steps:
1. Design Qualification (DQ): Confirmation of the suitability of the design
2. Installation Qualification (IQ): Confirmation of the suitability during installation
3. Operational Qualification (OQ): Confirmation of the suitability of operational performance design
4. Performance Qualification (PQ): Confirmation of the suitability during operation
These four steps are carried out as part of the validation process.