# Online GMP training & good manufacturing practices, ready to deploy.

The good-manufacturing-practices hub: GMP, sterile Annex 1 and data integrity. Micro-learning modules that are clear on the first read, aligned with inspector expectations, with an auditable certificate.

![Modern, sterile pharmaceutical production environment with digital training elements.](/assets/img/academy-bpf-gmp/hero-formation-bpf-gmp-en-ligne.webp)

## GMP isn't read, it's executed at the workstation.

Good manufacturing practices — **GMP** — govern every step of making a medicine: hygiene, gowning, process operation, documentation, batch management. On the floor, the challenge isn't knowing the standard — it's applying it the same way, by every operator, on every shift.

Effective **online GMP training** must therefore drill down to the exact move expected at the workstation, not stay at the level of principle. That's what Academy does: short, visual micro-learning programs, segmented by role, that turn a regulatory requirement into a daily reflex.

Three subjects structure this hub: **GMP fundamentals**, **sterile production (Annex 1)** and **data integrity** — the three areas where inspections concentrate the most findings.

100%

of staff must be trained for their activities, with a suitable level of education, training and experience — a GMP requirement, not an option.

Source: 21 CFR 211.25 (eCFR)

## The GMP programs.

Standalone modules or grouped into programs, from fundamentals to sterile expertise.

GMP

### GMP fundamentals

Principles, responsibilities, hygiene and documentation: the common foundation for all operators.

25 minBeginner

GMP

### Behavior in the production area

Gowning, flows, cross-contamination: the right moves in a controlled-atmosphere zone.

20 minBeginner

Sterile

### Annex 1: sterile production

Contamination control strategy (CCS), grades A to D, aseptic behavior.

35 minAdvanced

Sterile

### Aseptic technique & interventions in the clean zone

Interventions under laminar flow, media fill simulation, environmental alert management.

30 minAdvanced

Data integrity

### Data integrity & ALCOA+ principles

Attributable, legible, contemporaneous, original, accurate: securing data throughout its life.

22 minIntermediate

Data integrity

### Good documentation practices (GDocP)

Filling in a batch record, correcting an error, signing: the reflexes that avoid findings.

18 minIntermediate

[See programs by role →](/en/academy/roles/)

## Where inspections concentrate their findings.

### GMP fundamentals

The regulatory foundation and the daily moves: hygiene, documentation, process operation, batch management.

### Annex 1 — sterile production

Aseptic behavior and the contamination control strategy, the critical point of any sterile inspection.

### Data integrity

Data integrity and good documentation practices, at the heart of what the authorities expect.

## Your questions about GMP training.

Everything you need to know before deploying your programs.

What is the difference between GMP and cGMP? +

None in substance: GMP (good manufacturing practices) and cGMP (current good manufacturing practices) refer to the same set of requirements applicable to the manufacture of medicines, "current" simply emphasizing the up-to-date state of the art. Our modules cover both terminologies.

Who must take GMP training? +

Anyone whose activity has an impact on product quality: production, QA, QC, maintenance, logistics. The regulation requires that 100% of staff be trained for their activities, with initial and ongoing training (21 CFR 211.25).

Is the training auditable during an inspection? +

Yes. Each module ends with a quiz and issues a traceable, auditable certificate that stands up to inspectors, with a complete completion history — an audit-ready setup, integrable with your LMS via SCORM or xAPI.

Do you cover Annex 1 on sterile production? +

Yes. A dedicated program covers the contamination control strategy (CCS), cleanliness grades, aseptic behavior and interventions in a controlled-atmosphere zone, at the level of the move expected at the workstation.

How quickly can the programs be deployed? +

In a matter of days. The modules are ready to use: you choose your programs, assign them, and your teams learn. No content production to wait for, unlike in-house development.

## Explore our GMP catalog.

The full list of GMP, Annex 1 and data integrity modules, with durations and levels.