Product/Service

21 CFR Part 11 Software

Source: PANalytical BV
In addition to ensuring 21 CFR Part 11 compliance, PANalytical has extended its services for Design Qualification (DQ) and support for Performance Qualification (PQ). These add to our existing Installation Qualification (IQ) and Operational Qualification (OQ) documentation and support, helping users complete the qualification steps associated with validation.

Click Here To Download:
•Brochure: X-Ray Solutions For The Pharmaceutical Industry
•Corporate Brochure: PANalytical: At The Core Of The Matter

PANalytical supports the pharmaceutical industry in meeting today's requirements for:

  • the validation of analytical instruments
  • compliancy with the FDA regulations 21 CFR part 11 governing the use of electronic records and electronic signatures.
XRPD systems for the pharmaceutical industry come complete with software that incorporates full electronic signatures and audit trailing.

In addition to ensuring 21 CFR Part 11 compliance, we have extended our services for Design Qualification (DQ) and support for Performance Qualification (PQ). These add to our existing Installation Qualification (IQ) and Operational Qualification (OQ) documentation and support, helping users complete the qualification steps associated with validation.

Click Here To Download:
•Brochure: X-Ray Solutions For The Pharmaceutical Industry
•Corporate Brochure: PANalytical: At The Core Of The Matter