For a Healthier Tomorrow
AID Group combines pharmaceutical GMP expertise, engineering knowledge and project execution experience to support manufacturing facilities from concept and design through implementation, commissioning and qualification.
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For start-ups, foreign investors, and facility developers looking to build or expand compliant manufacturing facilities in Georgia.
For international pharma brands and global engineering firms needing an on-the-ground partner to execute local projects.
For existing local manufacturers optimizing infrastructure to meet international regulatory standards.
We work alongside manufacturers, equipment vendors and engineering partners across the region.
GMP readiness assessments, gap assessments and internal audits
Pharmaceutical facility concept development and layout planning
Vendor assessment, technical bid comparison and procurement support
Qualification and validation planning and execution support, including DQ, IQ, OQ and PQ
AID Group provides integrated consulting, engineering and qualification services for pharmaceutical manufacturing facilities. We help clients turn operational needs and regulatory requirements into practical, compliant and efficient facilities — from early concept and user requirements, through design and equipment/utility selection, to implementation support, commissioning, qualification and validation.
AID Group bridges the gap between pharmaceutical quality requirements and engineering execution. Our goal is to ensure that every technical decision supports not only project delivery, but also GMP compliance, operational efficiency, maintainability and successful qualification.
Planning a new facility or upgrading an existing one? Let's talk.
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