About GMP-Preinspection

Inspection Readiness Built by Those Who Have Stood on Both Sides

We are a specialist consultancy founded by former GMP inspectors and regulatory experts who understand exactly what authorities look for — and how to help your facility be ready.

Our Mission

Our Mission

GMP-Preinspection was founded on a single conviction: pharmaceutical manufacturers in the CIS region deserve access to the same level of inspection-readiness expertise that facilities in Western Europe and North America take for granted.

Our team brings decades of combined experience from regulatory authorities, multinational pharmaceutical companies, and contract manufacturing organisations. We have conducted inspections, received inspections, and guided facilities through every stage of the compliance journey.

We work exclusively in the CIS pharmaceutical space — not because it is the only market we know, but because it is the one where our expertise creates the greatest impact.

15+
Years of GMP Inspection Experience
Our lead consultants have collectively conducted and participated in over 200 GMP inspections across WHO, EU, PIC/S, and EAEU frameworks.
8
CIS Markets Served
From Uzbekistan and Kazakhstan to Russia, Belarus, Azerbaijan, Georgia, Kyrgyzstan, and Armenia — we know the regulatory landscape in each market.
4
Languages of Delivery
We deliver all services in Russian, Uzbek, Kazakh, and English — removing language barriers from the compliance process entirely.
Our Difference

Why Clients Choose Us

Former GMP Inspectors on Every Engagement

Every assessment is led by consultants who have personally conducted GMP inspections. We do not rely on checklists alone — we apply the inspector mindset to every evaluation.

Deep CIS Regulatory Knowledge

We understand the EAEU GMP framework, local authority expectations, and the practical realities of operating in CIS pharmaceutical markets — knowledge that generic consultancies simply do not have.

Multilingual, End-to-End Support

From the initial gap analysis through to CAPA closure and inspection day support, we work in your language. No translation delays, no miscommunication, no lost nuance.

Practical, Facility-Specific Guidance

We do not deliver generic reports. Every recommendation is tailored to your facility, your product types, your team, and your regulatory timeline.

Confidential and Independent

We operate with full confidentiality. Our only interest is your inspection success — we have no affiliations with regulatory authorities or competing consultancies.

Proven Track Record

Our clients have successfully passed WHO, EU, PIC/S, and EAEU GMP inspections following our pre-inspection engagements. Results, not promises.

Technical Depth

Our Areas of Expertise

Quality Management Systems
Documentation & Records Management
Production & Process Controls
Laboratory Controls & OOS Investigations
Facilities, Equipment & Utilities
Supplier & Material Controls
CAPA Systems & Effectiveness Checks
Validation & Qualification
Mock Inspections & Staff Training
EAEU & WHO GMP Regulatory Frameworks
Inspection Response & Authority Communication
CIS Market Regulatory Strategy
GMP-Preinspection multilingual consulting team
Language Capability

Multilingual Capabilities

Language is not a barrier — it is one of our core strengths. We deliver every service in the language your team works in.

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Russian
Primary working language across CIS markets
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Uzbek
Full service delivery for Uzbekistan-based clients
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Kazakh
Full service delivery for Kazakhstan-based clients
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English
International regulatory communication and documentation

Ready to Work With Us?

Tell us about your facility and your upcoming inspection. We will respond within one business day with a tailored proposal.

Request a Consultation