Medication repackaging
Compliant Repacking Aligned with GDP, GMP, and ISO 9001
Removing and replacing external packaging, updating information leaflets, and applying new labels etc.
Compliance and Security (Ensures adherence to industry standards of GDP (Good Distribution Practice, (GMP) Good Manufacturing Practice , ISO 9001 and provide audits for customer and his clients.
We provide:
- Manual and automated labeling
- Process controlled by experienced qualified persons
- Individually customizable process
Our quality asurace
Comprehensive Tracking and Quality Inspection
Item tracking, lot and expiry tracking quality inspections.
Handling Processes: Receiving to Packing
Handling (Recieving, inspecting, storing, picking, packing)
Worldwide distribution
Fast and reliable distribution to 140+ countries
IATA membership
IATA membership ensures safe, efficient, and compliant pharmaceutical air transportation.
GMP, GDP certificates
Our operations are certified according to Good Distribution Practice (GDP) and Good Manufacturing Practice (GMP) standards.
Customer experience
working with us
Dr. Chem Juris Hmeļņickis
AS “Grindeks” chairman of boardWe are a company with high standards, which we also demand from our partners. This is what “GDG” is like in organizing transportation – professional and reliable. We resolve any non-standard situations that arise immediately and carefully monitor high-quality documentation in all processes.
Egils Kopštāls
AS “KALCEKS” chairman of boardGeneral Development Group is a development-oriented and sustainability-minded company with which we always have successful cooperation in planning and conducting audits.
Pharmaceutical warehousing
Medication repackaging
SEA Freight
Road Freight transport
AIR Freight
oversized cargo transportation
Customs brokerageAbout Medication Repackaging
What is medication repackaging?
Medication repackaging is the controlled process of changing the external presentation of medicinal products without altering the product itself. It can include removing and replacing external packaging, updating information leaflets, applying new labels, and adapting packaging elements to meet specific market, regulatory, or customer requirements.
In regulated pharmaceutical operations, medication repackaging is not a standard warehouse activity. It is a compliance-sensitive process that must be performed within controlled procedures and documented quality systems. This is especially important when packaging changes affect product identification, traceability, or market readiness.
What medication repackaging may include?
- Removing and replacing external packaging
- Updating package leaflets and printed information
- Applying new labels to outer packaging
- Manual and automated labeling
- Customising packaging workflows for specific client requirements
GD Group provides medication repackaging services aligned with GDP, GMP, and ISO 9001 requirements. Its service scope includes replacing external packaging, updating information leaflets, applying new labels, and carrying out controlled repackaging processes adapted to client needs.
Why businesses use medication repackaging?
- To update external packaging in a controlled way
- To replace or revise information leaflets
- To apply new labels for specific market or operational needs
- To support traceable and documented repackaging workflows
- To align packaging activities with GDP, GMP, and ISO 9001 requirements
GD Group positions medication repackaging as a compliant process aligned with GDP, GMP, and ISO 9001. The company also provides audits for customers and their clients, supporting transparency and process review where required.
What should you look for in a medication repackaging provider?
Choosing a medication repackaging provider requires more than checking basic operational capacity. The provider should be able to demonstrate process control, qualified oversight, appropriate labeling capabilities, and a quality-focused approach suitable for regulated pharmaceutical products.
A reliable provider should also be able to adapt the repackaging workflow to different customer requirements while maintaining consistency and documented control.
Key factors to evaluate:
- Alignment with GDP, GMP, and ISO 9001 requirements
- Process control by experienced qualified persons
- Availability of both manual and automated labeling
- Documented and structured repackaging procedures
- Ability to adapt the process to specific client needs
Why choose GD Group for medication repackaging?
A medication repackaging partner should combine compliance awareness, practical process control, and flexibility. This is especially important for pharmaceutical businesses that need packaging changes completed within a documented and quality-controlled environment.
GD Group provides medication repackaging services with:
- Repacking aligned with GDP, GMP, and ISO 9001
- Removal and replacement of external packaging
- Updating of information leaflets
- Application of new labels
- Manual and automated labeling options
- Process control by experienced qualified persons
- Individually customisable repackaging workflows
- Audit support for customers and their clients
This makes GD Group relevant for companies looking for medication repackaging services carried out through a controlled, compliant, and adaptable pharmaceutical process.