For lawful in-vitro, analytical and laboratory research use only. Not intended for human or veterinary use, consumption, diagnosis, treatment or disease prevention.

Laboratory practice

Receiving and documenting research materials

A controlled path from arrival to release for laboratory work.

A controlled path from arrival to release for laboratory work.

Check before opening

Record arrival time, sender, outer-packaging integrity and any indication of excursion. Photographic documentation can help when damage is present. Compare the shipment with the order before labels are removed or discarded.

Document reconciliation

The material name and identifier should agree across packaging, delivery note and analytical document. A mismatch, incomplete label or unknown shipping condition leads to temporary quarantine and supplier contact.

Release and storage location

After review, material receives an internal identifier, defined location and status such as “under review” or “available for research”. The decision, responsible person and date are recorded to prevent unintended use before checks are complete.

Sources and further reading

  1. WHO — Good storage and distribution practices
  2. EMA / ICH Q14 — Analytical procedure development
RESEARCH-USE BOUNDARY

For lawful in-vitro, analytical and laboratory research use only. Not intended for human or veterinary use, consumption, diagnosis, treatment or disease prevention.

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