For organisations in the healthcare and pharmaceutical industry, ensuring good manufacturing practices (GMP) is essential. Testo's Validation service is designed to help businesses with GMP compliance for Therapeutic Goods Administration (TGA) or Food and Drug Administration (FDA) guidelines.
Alongside our excellent range of monitoring equipment, Testo's Validation service focuses on two critical areas - temperature mapping and equipment validation.
Any medical testing or pharmaceutical manufacturing facility requires strict control over environmental conditions, in particular temperature. Storage areas and laboratories must be kept within specific levels, ensuring the quality and safety of samples or products.
Temperature mapping involves the expert assessment of storage facilities, refrigerators and cold rooms, identifying where limits are required and installing the equipment to monitor them. This includes our range of temperature and humidity data loggers and monitoring systems, allowing users to observe fluctuations and be alerted when limits are breached.
Ensuring GMP compliance for temperature-sensitive pharmaceuticals must be a priority for any organisation in the industry - temperature mapping through Testo's Validation service makes that job easier
Having the right equipment is one thing; making sure it meets international regulatory standards and is in accordance with GMPs is another. With Testo's Validation service, experienced consultants will conduct an assessment of existing equipment to verify that it is up to the task.
Equipment validation involves the identification and examination of critical quality attributes (CQAs) and critical process parameters (CPPs) in pharmaceutical equipment, with specialist consultants able to identify risks and calculate the likelihood and impact of equipment failure.
Testo's Validation service provides the confidence and peace of mind that your equipment is safe and reliable enough to pass any auditing process.
