Skip to main content Skip to search Skip to main navigation

What are the quality requirements for pharmaceutical gases?

Unlike medical gases, pharmaceutical gases are not medicinal products. Therefore, the requirements must be defined according to the intended use of the gas itself. There are two categories "monographed gas" or "gas with product contact". The specifications are defined on a risk basis. Applying monographs can lead to increased testing effort and very strict specifications, so is not always sensible, but nevertheless necessary in individual cases.

[GMP Compliance AdviserChapter 3.H]

Would you like to discover more?

The GMP Compliance Adviser is the world's largest knowledge portal for quality management in the pharma business. 

The demo access is non-binding and ends automatically.

Test it now for free

You may also be interested in the following articles:

EMA: New Q&A on Product Lifecycle Management (PLCM)

EMA: New Q&A on Product Lifecycle Management (PLCM)

The EMA has published new Questions & Answers on the use of the Product Lifecycle Management (PLCM) document, clarifying its role within the EU variations framework for post-approval quality changes.
Read more
EMA: New Q&A for Co-Processed Excipients

EMA: New Q&A for Co-Processed Excipients

The EMA has published new Questions & Answers on co-processed excipients (CoPEs) used in solid oral dosage forms, introducing a harmonised, risk-based regulatory approach applicable to human and veterinary medicines.

Read more
What is the Data Lifecycle?

What is the Data Lifecycle?

Here's the answer:
Read more
Previous
Next