Category Archives: Qualification

10 Easy Steps – Deleting a Point from a Qualified Building Management System (BMS)

Siemens APOGEE

Hello, good people of the world! This post covers the procedure for deleting a point from a qualified Building Management System (BMS), specifically the Siemens APOGEE® BMS. A template for your use is here: Deleting a BMS Point TEMPLATE.

  1. Deleting a BMS Point Continue reading 10 Easy Steps – Deleting a Point from a Qualified Building Management System (BMS)

Fill Line Qualification

Aseptic Liquid Filling Line

Hello, good people of the world! This post is about aseptic liquid vial fill line qualifications. I’ve seen a few of these in my time, and in some ways they’re easier to qualify than other systems, in some ways more challenging. Fill lines may be easier because these systems are typically off-the-shelf with less customization. They may be more complicated because you’re dealing with a lot of interconnected equipment and automated control.

I’ve worked with Bausch-Stroebel (bausch-stroebel.com) and Bosch (bosch.com) fill lines, but TurboFil, Marchesini, and IMA are also common vendors.

The standard components of an aseptic liquid vial fill are: Trayloader/Unloader, Vial Washer, Depyrogenation Tunnel, Filler, Checkweigher, Stopperer, and Capper.

What considerations do you always keep in mind? Leave a comment below and please share this post with whomever you think would benefit..

Parts Washer Qualification – PQ

Parts Washer

This post is about Parts Washer qualification. This covers any manner of automated system that cleans parts out-of-place (Clean-out-of-place = COP). This includes process parts washers, glassware  washers, laboratory parts washers, etc. all of which may be termed COP washers.

The scope of a performance qualification of a washer is the performance of the equipment with defined recipe(s) and load(s). Be sure to capture the recipe and load configuration in the protocol prior to execution or as part of the execution itself. This is how the recipe and load configuration become “validated.” The recipe includes all steps and parameter values, and the load includes what parts or components will be washed and how they will be arranged. You’ll need to include a picture or diagram. Continue reading Parts Washer Qualification – PQ

URS for Purified Water Systems

WFI Still
WFI Still

Hello good people of the world! Today’s post deals with the User Requirements Specification (URS) for a Purified Water System. It may be RO/DI, Purified Water, or WFI, but it should probably have a URS. As with any URS, make sure requirements are specific, measurable, accurate, repeatable, and testable. Considerations specific to purified water systems include: Continue reading URS for Purified Water Systems

Qualifying cGMP Warehouse Space

Warehouse

Hello, good people of the world! So you have a cGMP warehouse you need to qualify? Well, this post will provide plenty of information to get you started.

First, how do you know your warehouse is a “cGMP” warehouse. Well, it is if:

  • The warehouse will house any raw material, excipient, intermediate, or finished product
  • The warehouse will house equipment or process consumables, such as filters, bags, disposable tubing, etc.
  • Any cGMP operations will occur in the warehouse, such as sampling, dispensing, kitting, track and trace, etc.

Any examples of common or even possible non-cGMP warehouse space in the Biopharma industry? Please leave a comment below.

Continue reading Qualifying cGMP Warehouse Space