We provide full-content clinical information to all our samples. We implement the project from the beginning to the end: from the project approval by the ethics commission to the completion and implementation of the plan.
By creating our own electronic database of all samples and clinical data related to various projects, we can easily provide complete information that interests the client.
Ethical Standards (IRB/LEC approvals, Consent documentation)
Study design; individual approach in close collaboration with the client
Preliminary pathology and histology review
Specimen recording, barcode labeling and scanning
Data management (collection of clinical information )
Freezer room monitoring and security, climate control
Packing and shipping
The following standard clinical information will be provided for each sample:
- Basic information (age, ethnicity, height, weight, gender)
- Date of sample procurement
- Clinical diagnosis (tumor location, type, stage, grade, TMN)
The pathology report can include: biomarker status (ER, PR, Her2) (not routine), the location of distant metastasis, the number of analyzed lymph nodes, the number of positive (metastatic) lymph nodes, tumor size.