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The Quality assurance program of Iris Pharma ensures that bioanalytical testing and studies are performed in complete compliance with GLP. Regular audits are carried out for each GLP study and bioanalytical testing (protocols, in-life phases, raw data, reports...), for different laboratory processes (management of test substances, animals, documentation, materials, waste, archives, samples...) and for internal technical training.

The company works in five complementary areas for a global drug development of eye product: bioanalytical testing and ocular Pharmacokinetics, preclinical formulation, preclinical services provider, clinical studies services and strategic consulting.

Efficient Bioanalytical Testing Laboratory

Iris Pharma performs bioanalytical testing in a GLP compliant laboratory. Iris Pharma has developed, adapted and validated the majority of essays for drugs and their metabolites used in preclinical and clinical studies:

• Toxicokinetics
• Preclinical and clinical Pharmacokinetics studies
• Bioavailability (BA)
• Bioequivalence (BE)

Bioanalytical Testing : Method Validation

Iris Pharma is a service provider of bioanalytical testing and validations. All of our methods for the bioanalytical testing are validated according to recognized international recommendations and guidelines before and during the bioanalytical testing.