About Erasmus Projects
Who We Are
Erasmus Projects CC is a specialist Information Technology partner for pharmaceutical manufacturers operating in GMP-regulated environments. With more than 15 years of direct experience inside pharmaceutical production facilities, we understand the operational, regulatory, and technical pressures that shape modern medicine manufacturing.
Our Experience
Our background includes hands-on support for:
Sterile manufacturing
API production
Packaging and serialization
QC laboratories and analytical systems
MES, SCADA, PLC, and OT networks
Validated computerised systems
SAHPRA inspections and GMP-aligned operations
We bridge the gap between IT, OT, Quality, and Production — helping manufacturers maintain secure, reliable, and compliant technology environments.
Local Presence, Practical Understanding
Our local Cape Town presence gives clients direct access to technical support that understands South African pharmaceutical manufacturing realities, including SAHPRA expectations, GxP documentation discipline, inspection readiness, and the practical coordination required across Engineering, QC, Production, Validation, and QA teams.
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Process Control Network design from scratch
Hands-on design and implementation of production networks, not advice from a distance.
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Enterprise Data Integrity strategy aligned to 21 CFR Part 11
Controls for electronic records, audit trails and access built as a strategy, not a patch.
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Deep QC laboratory instrument knowledge
Including Agilent, Shimadzu and related analytical systems and their data flows.
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Cross-functional experience
Working across Engineering, QC, Production, Validation and QA — the teams that have to agree.
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Local Cape Town presence
Practical understanding of SAHPRA, GxP and South African pharmaceutical manufacturing.
Our Mission
To strengthen pharmaceutical manufacturing operations through secure, compliant, and resilient IT systems that support quality, data integrity, and uninterrupted production.
Compliance Disclaimer
Erasmus Projects provides specialist Information Technology services that support GMP-regulated pharmaceutical manufacturing environments. Erasmus Projects does not act as the client's regulatory authority, Responsible Pharmacist, Quality Assurance department, validation owner, or legal advisor. Final responsibility for GMP compliance, SAHPRA submissions, validation approval, product release, and regulatory decisions remains with the licensed manufacturer and its appointed responsible personnel.
Work with a specialist
If your production environment is regulated, a generic IT approach shows up later in audit findings, downtime and rework.