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What needs to be validated in my product before I can commercialize it?

2 October 2018 - 16:05

Launching a product that touches the health sector means that you need to be compliant with a series of national and European laws, at the product level, but also during production, packaging and even at the level of the composition of the product. Therefore there are plenty of parameters that need to be investigated, from biocompatibility over the nature of the packaging, and the lifecycle to the sterilization process.

Tests and validations

In certain cases, the product also needs to pass through a series of tests and validations before being able to start commercializing it. Before doing the clinical tests, a pre-validation is sometimes necessary and can be done in different ways – laboratory tests, in silico tests, in vitro or even in vivo. It is one of the most complex aspects of entrepreneurship in the health sector and the consequences of the non-respect of certain processes can be extremely heavy.

The lifetech.brussels’ experts can help you in understanding the measures you need to take to make your product compliant and can accompany you in the validation process. They can also direct you to the specialists in the domain.

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