Removal

COREX Logistics will remove or accept drugs, equipment and clinical trial materials from research centers.

Before starting a clinical study, we study the SDS / MSDS forms (product certificate, which indicates the active ingredients and other parameters). This information is needed to determine if there are any risks during acceptance, which is especially important when it comes to toxic substances or opened packages. Based on these forms, we decide to accept the goods individually or locally.

Processes involved in return of drugs:

We receive the request from the client, which indicates the desired return time, detailed information about what exactly needs to be transported, in what volume and from where.

We agree with the research center on the date and time of pick-up for removal, clarify whether additional packaging materials are needed and space needed for storage.

We receive a return form signed by the client.

We accept returns at our designated return zone in our warehouses. We assign the status "returned product" to the cargo.

In the unloading area we measure the dimensions and weight of the goods. Next, we move the cargo to the return acceptance area, where the logistician accepts the cargo in accordance with the return form.

After acceptance, we send the cargo to the quarantine zone for storage of returns with controlled temperature conditions. Access to this area is restricted. The consignments are stored here until they are transferred for destruction.

Each return procedure involves three specialists: operator, logistician and pharmacist (or pharmacist):

the operator is engaged in unloading from the vehicle and placing in the receiving area;
a logistics specialist carries out direct acceptance;
a pharmacist or pharmacist performs final verification of the return.

OTHER SERVICES

Removal

Return, disposal and destruction of investigational products from clinical trials during and at the end of studies.

Veterinary

Full support provided for all aspects of clinical trials for veterinary and animal health products.

Purchase of orphan drugs

Procurement, supply, transport, storage and delivery of orphan drugs including regulatory processes.

Preparation of laboratory kits for clinical trials

All processes carried out in temperature controlled and secure warehouse facilities.

Working with labeled drugs in the MDLP system (Russia)

We have all the necessary technologies and experience to work with labeled goods.

Purchase of medicines and materials for clinical trials

We work directly with trusted manufacturers and authorized distributors.

Quarantine storage of drugs and clinical trial materials

Secure storage of all medicinal products in our network of warehouses in all temperature regimes.

Marking and labeling of medicinal products

In accordance with GxP standards.

Certified destruction of drugs

We manage returns and carry out certified destruction of drugs and materials during and at the conclusion of clinical studies.

CLINICAL TRIAL LOGISTICS

REGULATORY SUPPORT

CLINICAL STUDIES SERVICES

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Removal

Processes involved in return of drugs:

OTHER SERVICES

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