ICH Stability Storage Services

ICH stability storage services can significantly reduce costs and de-risk your pharmaceutical development program. Choosing to outsource should stem from strategic planning for your long-term stability needs and selecting the right vendor with GMP compliant facilities and highly trained staff experienced in managing complex stability studies is a key consideration. Outsourcing of stability storage allows you to focus on your core competencies whilst enabling a reduction in costs, demand for in house technology and staff resources and also free up precious real estate.

Sourcing suitable storage capacity can also be an issue for many pharmaceutical companies. Practical challenges such as the necessary footprint required to place new walk-in chambers, also include the cost of commissioning an in-house facility, the costs and resource demands related to validation and a continuous monitoring system to ensure they are 21 CFR part 11 compliant. It is also entirely likely that in the future you may require an expanded volume of storage making your current in house capacity no longer suitable. To overcome these challenges, partner with Intertek, a leading provider of outsourced stability storage. Our ICH stability storage services ensure adherence to regulatory requirements by providing controlled environments that are continuously monitored and validated. These services also offer scalability, allowing you to adjust storage capacity as your project needs evolve without the burden of infrastructure expansion. By leveraging a dedicated provider, you gain access to specialized expertise and advanced technologies, enhancing the reliability and accuracy of your stability data.

Outsourcing ICH Stability Storage Capacity
Our UK temperature controlled drug storage facility, located near Cambridge, is GMP compliant and is one of the largest storage facilities in Europe with 375,000L capacity. All climatic walk-in chambers, cabinets and refrigerated as well as freezer storage, are fully controlled and monitored with backup chambers. All sites have 24-hour alarm systems with dedicated on call teams to react to the excursions from storage conditions. We can provide ICH conditions or bespoke conditions storage supported by an experienced team who ensure that all 21 CFR part 11 monitored equipment is suitability qualified and validated. 

We consistently demonstrate excellence in project management and quality with a focus on knowledge of relevant ICH guidelines, clear understanding of our clients’ stability protocols or each stability disaster recovery client notification plan, excellent record of operation, maintenance and calibrations of stability chambers, freezers, and refrigerators alongside clear qualification documentation (IQ/OQ/PQ).

With nearly 30 years of experience, we have a proven track record in managing stability testing studies and providing Total Quality Assurance for controlled temperature and humidity storage stability storage for a wide range of global clients. We typically have over 300 studies in process at any time and our facilities have potential expansion capacity for an additional 300,000L if required. Contact our stability team now to find out how we can help you meet your stability storage needs.

Intertek Melbourn - Pharmaceutical Stability Testing and Storage