We understand that the Pharmaceutical Industry operates to extremely exacting standards and that patient safety and product quality is your primary concern.
Are you a Responsible Person (RP) or a Qualified Person (QP)?
As the RP or QP, we know that you are the principal custodian of these standards and that ensuring patient safety and product quality is your primary purpose. We also understand that satisfying the necessarily rigorous requirements and standards of the industry, is an extremely demanding responsibility and, with this in mind, it is our aim to support you, as a partner, in achieving these goals.
In executing this responsibility we appreciate that you have two main challenges namely:
- Counterfeit Product Detection
- Product Deterioration
The area in which we can assist you is Product Deterioration where our expertise in temperature and humidity monitoring is unsurpassed.
How do we do it?
We understand that the main components in the management of temperature and humidity standards for Controlled Temperature and Cold Chain Storage/Transport are:
- Temperature/Humidity Mapping
- Temperature/Humidity Monitoring
- Shipper Validation/Qualification
- Calibration
- Validation
Through many years of working in this area we have devised a range of solutions and services which supports the management of these critical areas.
We invite you to explore on this site the greater depth of information provided and we would welcome the opportunity to discuss your particular needs.
