Validation
Setting standards: Like all companies involved in the food and pharmaceutical industry, DISCH carries out validation. Validation involves documented proof of production processes, activities and manufacturing equipment. The reason for validation is not only, so that a process always produces the expected results, but so that quality and security is continuously adhered to. Especially in the pharmaeutical industry, it is very important that standards (GMP) are maintained.
A valid procedure
Just two steps lead to successful validation:
- compliance of the necessary documents, so that validation and production can always be achieved
- control of the validation process to meet the requirements of the GMP (Good Manufacturing Practice)
Areas studied under the magnifying glass
Validation and qualification at DISCH concerns the whole production area:
- manufacturing processes
- equipment and production machinery
- cleaning
- analytical methods
- packaging
Your product from A to Z
We offer the complete service – from concept to product launch. Your product is:
- manufactured to specific standards (food or GMP)
- certified by Swissmedic
Quality assurance
Additionally we carry out quality tests, stability studies and the development of testing methods to ensure quality remains constant.
What can we do for you?
Do you have questions about validation ? Further advice given freely on tel. +41 62 887 20 00 or info@disch.ch.
