Substantiate product locations, door influence, airflow and sensor positions in cold rooms where medicines, samples or temperature-sensitive products must remain within 2-8 °C.
Cold room mapping assesses whether relevant product storage positions remain within 2-8 °C during normal use. The study reviews door influence, evaporator or air outlet, airflow, height differences, loading, recovery after opening and the routine monitoring position. This clarifies suitable storage zones and any required restrictions.
For 2-8 °C storage, the focus is on product locations, door behaviour and airflow, not only the average cold room temperature.
Use the tool hub or create a 3D measurement-point proposal directly. It helps make room layout, product zones, doors and risks concrete before you choose a service level.
The dossier records why the measurement setup fits your cold room, which product locations were assessed and what the temperature data mean for 2-8 °C storage. Acceptance criteria are aligned with the stored products, room use and the audit or QA question.
For a 2-8 °C cold room, we look at the door zone, evaporator, return air, pallet or shelf height and existing sensor position. The dossier shows which zones are suitable and where routine monitoring makes sense.
The route stays the same, whether you measure yourself with rented loggers or outsource the full execution.
We map your room, limits and risks, and select the appropriate service level.
Measurement points, risk zones, measurement duration and acceptance criteria are defined in advance.
You measure yourself with rented loggers, or we come on site. The report is equivalent in both cases.
Data, analysis and conclusion in one report, ready for inspection or internal quality documentation.