About Product Safety Testing
Sequani
stands for something very special in worldwide product development.
Focused precisely on the needs of our customers, we have a highly
motivated team which harnesses the power and integrity of technology
to ensure timely and accurate delivery of products, offering seamless
integration across the boundaries of scientific disciplines.
For Consumer Product Evaluation, you won't find
better co-operation
Situated in a town at the centre of a rural community, we have a
volunteer base which other laboratories can only dream of. The stable
population provides us with people who have long-term associations
with Sequani, often through generations of the same families. They
have a relationship of trust with us which provides our clients with
maximum study flexibility, and outstanding volunteer compliance.
Best of all, sit down with us and talk
We are entirely flexible in the development of testing methodologies
and can customise protocols to match precisely the needs of a
particular product. Many clients tell us that this is the key to
their delight with our service. Sitting down and talking in our
relaxed and friendly environment can open up more possibilities than
first envisaged.
Preserving study integrity The
consistency and reliability of our volunteer pool enables us to ensure
compliance, attendance at our unit, and successful on-time completion
of studies. In order to protect the rights of the subjects and to
ensure the integrity of the data generated and reported it is the
policy of Sequani Limited to work to standards based on ICH Good Clinical
Practice Guidelines and Good Laboratory Practice regulations for
studies involving human subjects.
Define your study and
we will match the volunteers
From our thousands of volunteers, we can provide
virtually any subject profile you require. As well as usual adult
profiles, we can recruit groups from the elderly, infants and young
children. Our relationship with our volunteers normally means that
subjects can be available at short notice for study participation,
even for complex protocols. Lead times from as little as 1 week from
confirmation to study start, and a full
report within 2 weeks of completion. |
