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GMP LOGFILE Features

2017-07-19

LOGFILE No. 28/2017 – Checklist Performance Qualification

Checklist Performance Qualification

An Excerpt from the GMP Series PDF Download The Ultimate Checklist for Premises and HVAC Qualification

by Hans H. Schicht, PhD

 

Performance Qualification (PQ)

Performance qualification (PQ) is the documented proof that premises and utilities, in harmony with the production equipment, are suitable for manufacturing the product reproducibly in the specified quality. Performance qualification is the responsibility of the user of the facility and is initiated immediately after the transfer of facility ownership from the contractor to the user.

Regarding premises and the infrastructure systems installed therein, not many surprises are to be expected at that point in time. During operational qualification, air cleanliness measurements have been performed in the at rest occupancy state. During performance qualification, they are repeated in the in operation occupancy state, i.e. with the numbers of persons present as foreseen for normal production.

During PQ, the infrastructure systems and the process equipment operate, for the first time, as an integrated entity. For the first time, all machinery and other elements contributing to the heat load are now active in parallel. Therefore, only now it is possible to assess whether the HVAC system is capable of meeting its performance requirements at the extreme thermal load conditions regarding air temperature and air relative humidity specified for summer and winter as calculation base for dimensioning.

In addition, during performance qualification the human being is present for the first time in the facility in his condition as dissemination source for micro­organisms. Now, for the first time, is it possible to assess – where this is relevant – whether the limits established for microbiological monitoring are met. For sterile manufacturing, they are stipulated in Annex 1 to the EU GMP Guide (see Chapter C.6.1 and Chapter 3.C.2 GMP Requirements for Cleanrooms: Air Cleanliness Grades). In all other cases where microbiological risks have to be taken into consideration, they have to be specified case-specifically upon risk assessment considerations.

A selection of suggested PQ checks and tests is compiled in Figure 3.I-5. As now the manufacturing process and everything related to it is considered as an entity and as all interferences between the different elements of the premises, equipment, the HVAC system, process media and the human being are now fully effective, no longer a distinction is made in this table between the different infrastructure systems now acting together.

Figure 1: Checklist for performance qualification (HVAC related topics only)

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The Ultimate Checklist for Premises and HVAC Qualification provides you with all you need to know about:

  • Objectives of qualification
  • Regulative and normative fundamentals of qualification
  • Qualification master plan
  • Qualification plans and qualification reports
  • Requirements for measurement and test reports
  • Requalification

What's more, you will get detailed checklists for all qualification stages!

Author:

Hans H. Schicht, PhD
Management Consultant
Freelance, Zumikon, CH

Comments
Thank you for providing an excerpt , very helpful ,wish was more If you please provide pdf for printing would be appreciated
hilda adibpour 2017-07-26
 
Maas & Peither GMP Publishing: Thank you very much for your comment and your interest in our Newsletter LOGFILE. Please find attached a pdf version of our feature in LOGFILE 28/2017. For extracts from our publications we usually do not prepare an extra pdf document. We publish the text online on our website. Thanks for your request for a printable version (pdf format). We will reconsider publishing every time also a pdf document.
Editorial Office Maas & Peither GMP Publishing 2017-07-27
 
 
 
Literature recommendation
The Ultimate Checklist for Premises and HVAC Qualification
GMP Compliant Documentation
GMP Compliance Adviser
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