About QualiPharma
QualiPharma is a healthcare software platform from QualiSanté that supports patient management. It provides functionalities such as Dossier Patient Informatisé, Pédiatrie, Urgences, and Psychiatrie so healthcare professionals can access and manage patient information efficiently. The platform is designed to facilitate better communication and coordination among diverse medical specialties. With options tailored to various departments, it helps improve workflow and patient care. Key capabilities: Fonctionnalités À propos Pédiatrie Urgences Psychiatrie Best for: healthcare providers that need an integrated solution for patient records and departmental collaboration.
QualiPharma is an essential "compliance engine" for pharmaceutical companies operating in French-speaking markets. It successfully digitizes the complex Good Manufacturing Practices (GMP) that govern drug safety. Its standout feature is the integrated Change Control and Pharmacovigilance modules, which provide a level of security and traceability that manual systems cannot match. While it requires a disciplined implementation, it transforms Quality Assurance from a bureaucratic hurdle into a proactive competitive advantage, making it a top-tier choice for labs aiming for international excellence.
Pros & Cons
- Greatly reduces the physical footprint of batch record storage.
- Moves the lab from reactive testing to proactive quality assurance.
- Specifically built for GxP and pharmaceutical legal frameworks.
- Users need a strong background in pharma quality to navigate the advanced features.
- Support and pre-templates are heavily optimized for French/North African regulations.
- The high level of compliance requires a very structured initial setup.
Features
Key features
Pre-configured workflows designed to satisfy "Good Manufacturing Practices" (Bonnes Pratiques de Fabrication) requirements for drug production.
A rigorous system to manage modifications in production processes, equipment, or materials to ensure no impact on drug quality or safety.
Tools to collect, track, and report adverse drug reactions to national and international health authorities.
Manages data related to batch testing and stability studies, ensuring products remain safe throughout their shelf life.
Automates the identification of production deviations and tracks the corrective and preventive actions required to resolve them.
Additional features
Centralized management of SOPs (Standard Operating Procedures) and master batch records.
Scheduling and execution of internal quality audits and supplier audits.
Compliant with 21 CFR Part 11 style requirements for digital validation.
Tracking staff certifications and mandatory GxP training records.
Managing and auditing third-party raw material and API providers.
Tools for pharmaceutical quality risk management.
Automated alerts for the maintenance of lab and production machinery.
Tracking cleanroom conditions (temperature, humidity, particles).
Centralized tracking of all quality tasks across the laboratory.
Real-time data visualization of quality trends and compliance status.
Pricing
Countries & Languages
Available in
Interface languages
Billing currencies
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About QualiPharma
QualiPharma is a healthcare software platform from QualiSanté that supports patient management. It provides functionalities such as Dossier Patient Informatisé, Pédiatrie, Urgences, and Psychiatrie so healthcare professionals can access and manage patient information efficiently. The platform is designed to facilitate better communication and coordination among diverse medical specialties. With options tailored to various departments, it helps improve workflow and patient care. Key capabilities: Fonctionnalités À propos Pédiatrie Urgences Psychiatrie Best for: healthcare providers that need an integrated solution for patient records and departmental collaboration.
QualiPharma Details
QualiPharma's In-App Market Place
Does QualiPharma have an in-app market place?
Yes
How many Mini-Apps in the marketplace?
1
Mini Apps
N/A
Pricing Options
Accepted Payment Currencies
EUR (), DZD ()
Pros & Cons
- Greatly reduces the physical footprint of batch record storage.
- Moves the lab from reactive testing to proactive quality assurance.
- Specifically built for GxP and pharmaceutical legal frameworks.
- Users need a strong background in pharma quality to navigate the advanced features.
- Support and pre-templates are heavily optimized for French/North African regulations.
- The high level of compliance requires a very structured initial setup.
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