Our Quality Control service is in charge of in-process
control of the manufacturing, packaging and distribution
activities. As a pharmaceutical establishment, we are
also able to provide control for commercial drugs.
QP Services:
Since May 1st, 2004, Investigational Medicinal Products
manufactured outside EU borders have to be imported
and released by a Qualified Person (QP) in Europe (European
Directive 2001/20/EC).
The QP is responsible for the compliance of the imported
product with European regulations and guidelines.
This Directive has a major impact on non European sponsors. CRID PHARMA
proposes QP release services and has 2 Qualified Persons
with comprehensive experience of European regulations
and work on a daily basis with International clients.