What evidence should state
Issuer, audited organisation, address, activity, standard reference, issue and expiry dates and restrictions must fit the intended service.

No blanket certification claims
The phrase GDP-certified is often used too broadly. Reliable evidence must cover the actual organisation, site, activity and validity period. Inter-Pharma therefore describes its own processes as GDP-oriented and confirms applicable evidence per project.
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Issuer, audited organisation, address, activity, standard reference, issue and expiry dates and restrictions must fit the intended service.
Storage evidence does not automatically cover transport. Carriers, networks, subcontractors and their qualifications are reviewed separately.
Inter-Pharma performs warehousing, inventory control, picking, pack checks and dispatch preparation in Cheb under GDP-oriented requirements. We do not claim blanket GDP certification.
Product, temperature, site, scope, responsibility, evidence and quality agreement are documented for the project before operations start.
1. Match the organisation and exact site address. 2. Distinguish a wholesale distribution authorisation, an official GDP certificate and a commercial certificate. 3. Check activity, product, temperature, storage and transport against scope. 4. Review dates, validity, restrictions and non-compliance records. 5. Verify partners and subcontractors separately and record accepted evidence in the quality agreement.
Central European location
Cheb lies in western Czechia, directly at the German border. The location connects Bavaria, Saxony, Austria and Poland with short access routes to Central and Eastern Europe.
Approximate straight-line distances, rounded to 10 km. Actual road distances vary by route.
This is how we structure delivery. Before start, we agree which steps belong to us, the client or a partner.
Record current operations, retained and outsourced tasks, locations, volumes, risks and owners. Assign storage, order handling and transport separately.
Deliverable: A task and responsibility matrix.
Together we define acceptance conditions, operator and client roles, authorisation scope, release decisions, deviation routes and required evidence.
Deliverable: Agreed scope and quality agreement.
Assess specifications, capacity, mapping, monitoring, alarms, escalation and handovers before acceptance. Explicitly agree refrigerated storage and staging times.
Deliverable: A confirmed temperature and handover profile.
Agree item, batch, expiry, stock and order data with your systems. Test formats, validation, status messages and exception handling.
Deliverable: Accepted data fields and tested interfaces.
Run an agreed test case through the intended steps. Check data, traceability, handovers and failures; start after documented acceptance.
Deliverable: Accepted operating scope and confirmed start.
Compare stock, order status and agreed indicators. Follow deviations, causes, actions and owners through the agreed review cycle.
Deliverable: Traceable actions and updated planning.
Agree products, tasks, authorised contacts, evidence, data handovers and acceptance criteria. Dates and capacity follow the confirmed scope.
We structure your needs and connect the right partners and processes.