
Pharmaceutical
R&D, regulatory affairs, QC, QA, microbiology and ERP on one platform, built for EDA GMP, EGAC ISO/IEC 17025, FDA 21 CFR Part 11 and EU Annex 11.
The same integrated platform, configured for the way your industry tests, releases and documents product.
Every industry below runs on the same CORPEX core: a LIMS for the lab, an electronic QMS for quality assurance and an ERP for operations. What changes is the workflow, the regulations it has to satisfy and the evidence an auditor will ask for. Each page explains what that looks like in practice.

R&D, regulatory affairs, QC, QA, microbiology and ERP on one platform, built for EDA GMP, EGAC ISO/IEC 17025, FDA 21 CFR Part 11 and EU Annex 11.

Raw-material, in-process and finished-goods testing with document control and ERP, supporting HACCP and ISO 22000 food-safety programmes.

Quality control, quality assurance and process management for chemical manufacturers, from incoming material to certificate of analysis.

BioLIMS for bioequivalence and bioavailability studies and MicroLIMS for microbiology testing, with GLP-ready audit trails.

ERP, quality control and quality assurance for manufacturers outside pharma: production planning, supplier quality and compliance records.
No. Pharmaceutical manufacturing is where the platform started, but the same LIMS, eQMS and ERP modules are used in food and beverage, chemical, bioanalytical and general manufacturing settings. The workflows and compliance templates are configured per industry.
It supports FDA 21 CFR Part 11 and EU Annex 11 for electronic records and signatures, ISO/IEC 17025 for testing laboratories, EDA GMP in Egypt, and food-safety programmes such as HACCP and ISO 22000.
Yes. A group that runs, for example, a pharmaceutical plant and a food plant can run both on one CORPEX installation, with separate workflows, specifications and approval routes for each site.
Tell us what your lab or plant runs today and we will show you how it maps onto CORPEX.
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