# Your GMP compliance rests on critical actions. Secure them.

In pharmaceutical production, GMP compliance plays out at the workstation: on an intervention in a sterile area, a weighing, a batch-record review, a deviation handling. This critical know-how stays largely informal, in the heads of your experienced operators, your QA and your QC. Sinfony captures it so that mastery — and data integrity — no longer depend on key people.

![Sterile pharmaceutical production environment illustrated in a modern, clean style](/assets/img/secteurs-pharmaceutique/hero-industrie-pharmaceutique-gmp.webp)

## Validated doesn't mean mastered.

Your SOPs are approved, your training records signed off. But between the procedure and the real action in sterile production, the gap remains — and it fuels deviations, recurring CAPAs and inspection observations. Data integrity, asepsis and batch release demand a consistent execution that documentation alone cannot guarantee.

100%

of staff must be trained for their activities: a GMP requirement, not an option.

Source: 21 CFR 211.25 (eCFR)

80%

of critical know-how stays informal, held by a few operators and QA/QC experts.

Sinfony field observation

### Deviations & CAPA

Cut recurring deviations by tackling the root cause: the poorly transmitted action.

### Data integrity

Embed the right ALCOA+ reflexes into daily practice at the workstation.

### Sterile production

Secure aseptic interventions through the filmed, standardized action.

## Capture GMP know-how, for the long run.

Three complementary levers, from ready-to-use content to field consulting.

[Training

### Academy

Ready-to-deploy GMP and pharma-quality modules: data integrity, deviations, QA/QC, in-area hygiene.

Explore the catalog →](/en/academy/) [Platform

### Learning Suite

Auditable certificates and audit-ready traceability to prove every operator's qualification.

See the platform →](/en/learning-suite/) [Consulting

### Consulting

Field assessment, deviation reduction and SOP simplification, with the method transferred to your teams. From €5k.

Request an assessment →](/en/consulting/)

## The proof, in numbers.

What pharmaceutical sites see once their critical actions are captured.

−15 to −30%

deviations

−50%

deviation handling time

−95%

training-related errors

20,000

certificates that stand up to inspectors

> "You're the consultants with the nerve to actually make things move."

Novo Nordisk

## Request an assessment.

A Sinfony expert reviews your deviations, your SOPs and your critical GMP actions with your teams.