Particle analyses are typically used in registration documentation and quality control. Consequently, the generated data have to live up to official standards, and the laboratory quality system must comply with the quality demands of the customer. First every task is carefully stipulated so that PARTICLE ANALYTICAL can meet the individual customer’s requirements for quality control and reporting, enabling easy integration of data into the customer’s documentation system.


PARTICLE ANALYTICAL ApS is approved as a GMP laboratory by the Danish Medicines Agency.
The approval applies for both human and veterinarian medicinal products and is valid until March 1st 2012.
Please click here to request the certificates.