Digital Solutions for the Pharmaceutical Industry
In a sector where regulatory compliance, total traceability, and quality control are essential, Geprom offers solutions that ensure product integrity, reduce errors, and facilitate the validation of critical processes in highly regulated environments.
How Geprom Helps your Pharmaceutical Industry
Geprom works alongside companies in the pharmaceutical and biotechnology sector, providing platforms that guarantee compliance with GMP, FDA, ISO, and GxP regulations. Our solutions integrate batch traceability, real-time quality control, and advanced document management, reducing risks, ensuring regulatory compliance, and optimizing production in sensitive environments.
Challenges of the Pharmaceutical Sector
Compliance with regulations such as GMP, GxP, FDA, or ISO
Rigorous and standardized processes to guarantee quality, safety, and legality.
Complete Batch Traceability and Production Record
Exhaustive tracking from raw material to final product.
Quality Control and Non-Compliance Management
Constant supervision to maintain product integrity.
Supervision of Environmental Conditions (Clean Rooms)
Strict control of temperature, humidity, and purity in critical environments.
Document Validation and Sterile or Personalized Production
Exhaustive management of documentation and critical production processes.
Benefits of our Solutions
-
Simplified document auditing and guaranteed compliance
Total transparency and traceability in each stage of the process. -
Reduction of human errors and non-conformities
Automation of controls to reduce risks and failures. -
More agile and safe production
Optimization of processes without compromising safety standards. -
Improvement of traceability and documentation
Detailed record for audits and regulatory compliance. -
Cost savings through preventive control
Anticipated supervision that reduces stoppages and errors.