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

Receiving and documenting research materials

A controlled path from arrival to release for laboratory work.

01Check before opening

Record arrival time, sender, outer-packaging integrity and any indication of excursion. Photographic documentation can help when damage is present. Compare the…

02Document reconciliation

The material name and identifier should agree across packaging, delivery note and analytical document. A mismatch, incomplete label or unknown shipping…

03Release and storage location

After review, material receives an internal identifier, defined location and status such as “under review” or “available for research”. The decision,…

01

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.

02

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.

03

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.

LABORATORY APPLICATION

Turning the principle into an auditable record

Use one receipt form covering order, sender, date and time, packaging condition, label, documents, transport condition, excursion, temporary location and final decision. Photographs are attached when an issue exists and retained with the event.

01Opening before recording outer condition
02Silently correcting a mismatch
03Use before documented release

PRIMARY & OFFICIAL SOURCES

Sources and further reading

  1. 01WHO — Good storage and distribution practices↗
  2. 02EMA / ICH Q14 — Analytical procedure development↗

COMMON QUESTIONS

Questions specific to this topic

What is recorded before opening?

Time, sender, outer integrity, seals and any indication of excursion.

What happens after a label mismatch?

The material is segregated and documented clarification is requested before release.

Why use an ‘under review’ status?

It prevents unintended use until administrative and technical checks are complete.