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OPIS commitment is to offer the best possible quality
while ensuring maximum flexibility towards our Customers’
needs, always in compliance with Good Clinical Practice and
Standard Operating Procedures (SOPs – internal or supplied
by the Customers).
Our procedures are constantly monitored and
reviewed, and mirror the specifications of all the
Regulatory Boards relevant to scientific and ethical quality
standards.
The extensive experience achieved makes our offer up
to the highest quality levels along all the stages of the
clinical trial process, together with the specific medical
and statistic competence of the senior management assisted
by a staff of more than 115 collaborators periodically
trained.
Our Quality System is constantly verified through
internal audits and periodical audits carried out by partner
pharmaceutical companies, thus ensuring steady quality
development.
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