Effortless Cleaning validation,
no stress - no Excel

Yes. Hally-pharma is designed to be compliant with FDA 21 CFR Part 11 and EU Annex 11, while adhering to the cleaning and validation best practices outlined in industry reference technical guides (PDA, ISPE, A3P, etc.). The electronic audit trail and full traceability are native to the platform — not features to configure

Sign up in seconds — no credit card required. You immediately access a full demonstration environment with a preconfigured project, representative of a real cleaning validation case, where you can test all features with your own data — up to 3 finished products, 10 pieces of equipment, and 2 manufacturing processes.

Hally-pharma is a cloud solution, operational in a few hours. No infrastructure to install, no server to manage. Our team guides you step by step during onboarding so you become autonomous as quickly as possible.

The security of your data is our priority. We host our services in France on ISO 27001-certified infrastructure and enforce strict access controls. Regular cybersecurity audits and automatic backups ensure the integrity and availability of your information.

Yes. Hally-pharma is designed to adapt to both start-ups and large international pharmaceutical groups. The offering is modular based on your number of users, projects, and specific needs. Contact us for a custom quote.

A project is a work environment centralizing all the information needed to define a common cross-contamination acceptance criterion.

Do you have two production lines that share products and equipment? That's a single project. Do you have two production lines that share neither products nor equipment? Those are two separate projects.

Hally-pharma is designed to handle any configuration, even the most complex ones, starting with an unlimited number of product combinations. Whether you have 2, 10, 50, or 1,000 products, Hally-pharma is fully capable of managing all combinations without compromising on performance or accuracy.