Ramping Chamber Validation

Conduct Stability Tests with Confidence in the Accuracy of Your Ramping Chambers

Ramping chambers or cycling chambers play a crucial role in stability testing to identify product storage conditions, simulate logistic studies, and more. These chambers either approach a set temperature at a specified rate and maintain that temperature for a specified length of time or go through cycling programs that can ramp through an array of different temperatures at predetermined periods of time. If this piece of equipment is not in compliance with your SOPs and cGMP regulations, your drug study could be in serious trouble. Masy helps you keep your products safe and conduct precise stability testing procedures by providing industry-leading validation solutions for your ramping or cycling chambers.

When you partner with Masy BioServices for your ramping chamber validation projects, we give you the peace of mind that your chambers work appropriately and reliably. Whether you want us to work independently or with your facilities team, we are committed to providing the highest level of service and value in optimizing your ramping chamber’s performance.

Our Approach to Ramping Chamber Validation

We can execute many chamber mapping studies simultaneously with access to over 100 data acquisition systems and hundreds of DataTrace wireless dataloggers. This efficiency saves you time and money on our ramping chamber qualification or other validation projects. We also leverage our experience to recommend and implement modifications to your chamber, so we can ensure your chamber is in compliance even before qualification begins.

Industry-Leading Ramping Chamber Validation Practices

When you need ramping chamber validation, Masy is the best choice. We deliver the Masy level of quality every time. You can count on Masy to be your trusted advisor in qualification and validation, whether we are making sure that your equipment is qualified, or we are providing the options to get it there.

Time is valuable in a high-demand, fast-paced industry. Masy creates time and money-saving efficiencies in the validation process by conducting pre-qualification procedures before beginning a project. Pre-qualification assesses your equipment’s performance before validation begins and determines if the equipment will likely pass or fail validation – helping you make the most informed decision before moving forward with further testing.

All certified validation and calibration equipment used at customer sites is verified upon return to our NVLAP accredited metrology laboratory to confirm accuracy (NVLAP lab code 200904-0). We complete your project by providing a clear, comprehensive validations report, confirming your equipment is fit for use for your requirements. 

Reducing equipment downtime is critical to meeting the needs of patients. Masy is fully equipped with an in-house validation team and the largest validation equipment inventory to consistently meet or exceed your project and time-frame requirements, while never sacrificing quality or accuracy.


Learn more about the validation solutions we provide by downloading our brochure about ramping chamber validation. 

Masy can be your bio solutions provider for any need.

We are an all-encompassing bio solutions partner, offering services for calibration, monitoring, biopharmaceutical storage, validation, and product rental & sales. Improve the efficiency of your operation and products when you choose Masy as your single-source bio solutions provider.



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