Your quality manager

The regulatory requirements are high for businesses in the Life Science industry. Many smaller businesses find it very demanding having to continuously be up-to-date on new laws and regulations. When the Medical Device Directive was revised in March 2010 it became clear that many businesses, especially Class I manufacturers, were caught by surprise and were not prepared for this; many have still not implemented all the new changes required by law, for instance updating of the technical files for their products.

Most of Symbioteq’s clients are small to medium sized businesses. We know all about the difficulties and costs involved having the expertise in-house.

You might want to consider if it is not more cost effective to hire one of our consultants instead! They are continuously updated on any changes in the market and how to best implement them.

We have clients who hire us full-time, part-time, one or two days a week or perhaps only a couple of days every month. It all depends on your business, your needs and on the kind of products you are manufacturing.

A flexible solution will give you the support you need, when you need it!