| Feature | Description |
|---|---|
| Camera Support | Simultaneous connection with up to 4 smart cameras |
| Device Compatibility | Full compatibility with Cognex In-Sight cameras and Dataman barcode readers |
| Compliance | Full compliance with CFR 21 Part 11 standards |
| User Management | 7 authorization levels, password policies, session management |
| Reporting | PDF outputs, operation history, and error analysis |
| Data Security | Automatic backups, encrypted data storage, offline access restriction |
| Interface | Operator-friendly, simple, and intuitive design |
CheckPharma | Image Processing and Quality Control Software
CheckPharma is an advanced software that provides real-time quality control on pharmaceutical production lines, integrated with image processing technologies. Working in harmony with smart camera systems, this solution delivers accuracy, speed, and reliability at every stage of production.
Standardize Quality in the Pharmaceutical Industry
Today, pharmaceutical manufacturing operates at high speeds, and supporting this pace with reliable quality control mechanisms is essential. In industries like pharmaceutical production, which directly impact human health, ensuring that products are manufactured completely and without defects is of utmost importance. This is where CheckPharma comes in—offering full regulatory compliance and enhanced production efficiency.
Versatile and Flexible Inspection Structure
CheckPharma performs numerous quality control steps—such as blister filling inspection, ampoule print verification, liquid level measurement, and barcode checking—within seconds and with high accuracy. Its ability to manage up to four different smart cameras simultaneously from a single screen reduces operator workload and lowers system costs.
Operator-Friendly Interface
With its streamlined and intuitive design, the software’s user interface makes operation easier for personnel. Training times are shortened, operational errors are minimized, and the interface can be customized to suit specific production needs.
Technical Specifications
Advanced Security and CFR 21 Part 11 Compliance
CheckPharma is developed in full compliance with FDA standards (CFR 21 Part 11). Every action is recorded in an immutable format, along with the username, timestamp, and details of the operation. These records can be automatically reported in PDF format.
With up to 7 levels of user authorization, password policies, session timeouts, and secure access protocols, data security is ensured at the highest level.
Actions Implemented Under CFR 21 Part 11 Compliance:
Recording of operation steps in internal memory along with time and user information (audit trails).
Recorded data cannot be altered or deleted retrospectively. Records can be exported in PDF format.
Backups of records can be taken automatically at specified intervals or on demand.
Ability to define different users with 7 different authorization levels.
Determination of accessible features within the program based on a user authority matrix, according to the user’s authorization level.
Ability to set minimum password requirements for user accounts (e.g., password length, inclusion of uppercase letters, numbers). Newly created users are required to set their own passwords.
Obligation to set a new password after a defined period.
Automatic account lockout after a specified number of incorrect password attempts, with reactivation only by an authorized user.
Inability to delete created user accounts; authorized users can lock and unlock them as needed.
