Your (lab) equipment ready all the way
Guaranteeing the quality of the final product is of essential importance in the pharmaceutical sector. That is why you work with highly reliable devices and also why flawless validation is indispensable. Through a series of procedures and tests your dedicated Advipro expert validates whether a device meets all the requirements of both external regulations and the customer. A matter of achieving the intended quality time after time.
The initial validation of a device shows that it complies with company rules and industry standards. As well as the requirements of certain ISO standards. Thereafter, the Advipro team will continue to monitor the correct operation of the device through periodic checks. Our clear procedures are your guarantee of proper use of the devices. Always kept in top condition, allowing your business to produce in all safety.
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"With Advipro, you rely on a team of passionate engineers. All of them experienced experts within the life sciences industry. Each with their own specialities.”Julie - Senior Project Engineer
Equipment validation – Advipro @ your service
- Professional support throughout the life cycle of your device, including:
- Selection & purchase of appliances
- Release for use & periodic in-use validations
- Correctly withdrawing from service through decommissioning
- Accurate documentation according to applicable GDP rules
- Development of a validation plan for each specific type to ensure sustainable use, including:
- User Requirement Specifications (URS) to be met by the device
- Risk analysis
- How the device will be tested
- Overview of tests
- Final report for release
- Preparing a user procedure
- Planning necessary periodic maintenance with all parties involved, taking into account:
- Lab technicians
- Operators
- Technicians
- Validation engineers
- Preparation of corrective and preventive actions to handle and prevent deviations correctly
- Documentation of changes using change controls
