📅 Compressed Air Testing Training - 10–11 Jun 2026. Limited seats. Reserve My Seat →
GMP Training Course

Compressed Air Testing & Qualification Training

Instructor-led training covering pharmaceutical compressed air purity testing, ISO 8573 standards, EU GMP Annex 1 requirements, sampling methodology, qualification protocol writing, and documentation. Online and on-site delivery.

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Online & On-Site English & Arabic ISO 8573 & EU GMP Annex 1 Certificate of Attendance
Course Modules

What this training covers

Practical, regulation-aligned content covering compressed air qualification from regulatory requirements through hands-on protocol execution and documentation.

Module 1

Regulatory Requirements

  • EU GMP Annex 1 (sterile manufacturing)
  • EU GMP Annex 15 (qualification)
  • ISO 8573 compressed air purity classes
  • Pharmaceutical utility qualification expectations
Module 2

Purity Testing Methods

  • Particulate testing and particle counting
  • Moisture / dew point measurement
  • Oil content analysis
  • Microbial contamination testing
Module 3

Sampling Strategy

  • Worst-case sampling point selection
  • Sampling frequency requirements
  • Equipment and sampling technique
  • Acceptance criteria setting
Module 4

Qualification Protocols & Documentation

  • Compressed air qualification protocol structure
  • IQ/OQ for compressed air systems
  • Data recording and report writing
  • Ongoing monitoring programme
Register

Reserve your seat - Compressed Air Testing Training

10–11 June 2026. Fill in your details below and we will confirm by WhatsApp or email within hours, and send pre-reading materials before the session.

10–11 June 2026 · Limited Seats
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FAQ

Compressed air training questions

QA managers, CQV engineers, engineering staff, and production supervisors responsible for compressed air systems in pharmaceutical and sterile manufacturing environments.
Compressed air testing is the analytical sampling of air purity parameters (particles, moisture, oil mist, microbiological content). Compressed air qualification is the broader GMP process - risk assessment, IQ/OQ of the system, and the formal testing programme documented in a qualification protocol and report.
ISO 8573 defines purity classes for particles (0–9), water/humidity (0–9), and oil (0–4). In pharmaceutical manufacturing the applicable class depends on the point of use and GMP risk - direct product contact requires the highest purity. The training covers class selection, sampling, and verification for each application.
Yes. The 2022 Annex 1 revision requires a formal Contamination Control Strategy (CCS) that addresses compressed air as a contamination route. The training covers the Annex 1 requirements and how to integrate them into your qualification and monitoring programme.
Yes - PHARPRO delivers online (live instructor-led) and on-site at your facility. On-site allows practical exercises using your actual compressed air system drawings and P&IDs. Contact us to discuss dates and format.
Yes - Arabic-medium private sessions are available for pharmaceutical teams across Jordan, Saudi Arabia, UAE, Egypt, and the wider MENA region.
A PHARPRO Certificate of Attendance documenting the course title, content summary, delivery date, and instructor credentials - suitable for GMP training files and regulatory inspection review by FDA, EU GMP, WHO, or JFDA.

More questions

Who should attend the Compressed Air Testing training?

This course is designed for QA managers, CQV engineers, engineering staff, and production supervisors responsible for compressed air systems in pharmaceutical and sterile manufacturing environments.

What standards does the training cover?

The training covers ISO 8573 compressed air purity classes (particles, water, oil), EU GMP Annex 1 requirements for sterile manufacturing utilities, and pharmaceutical good practice for compressed air qualification - including risk assessment, sampling procedures, and acceptance criteria.

Can this training be delivered on-site at our facility?

Yes - PHARPRO delivers this training on-site at your pharmaceutical facility as well as online in live instructor-led sessions. On-site delivery allows practical exercises using your actual compressed air system drawings and P&IDs.

What is the difference between compressed air testing and compressed air qualification?

Compressed air testing refers to the analytical sampling and measurement of air purity parameters (particles, moisture, oil mist, microbiological content). Compressed air qualification is the broader GMP-documented process that includes risk assessment, installation and operational qualification of the compressed air system, and the formal testing programme with acceptance criteria referenced in a qualification protocol and report.

What are the ISO 8573 compressed air purity classes for pharmaceutical manufacturing?

ISO 8573 defines purity classes for three main contaminants: solid particles (classes 0–9), water/humidity (classes 0–9), and oil (classes 0–4). For pharmaceutical manufacturing, the applicable classes depend on the point of use and GMP risk - direct product contact applications typically require the highest purity. The PHARPRO training explains how to determine the right purity class for each application and how to verify compliance through sampling and analysis.

Does EU GMP Annex 1 (2022) affect compressed air requirements?

Yes. EU GMP Annex 1 (2022 revision) has strengthened requirements for compressed gas systems used in sterile manufacturing - including the need for a formal Contamination Control Strategy (CCS) that addresses compressed air as a potential contamination route. The PHARPRO Compressed Air Testing training covers the Annex 1 requirements and how they apply to your qualification and monitoring programme.

What certificate do participants receive for compressed air testing training?

All participants receive a PHARPRO Certificate of Attendance documenting the course title, content summary, delivery date, and instructor credentials. This serves as verifiable evidence of GMP training for annual training files and regulatory inspections by FDA, EU GMP authorities, WHO, or JFDA.

Is the compressed air training available in Arabic?

Yes - PHARPRO delivers this training in English and Arabic. Arabic-medium sessions are available for private and on-site engagements, serving pharmaceutical teams across Jordan, Saudi Arabia, UAE, Egypt, and the wider MENA region.