Ordering Info

CiceroDx provides all supplies necessary for proper submission to our testing facility. This includes our ReceptivaDxTM Collection Kits, Test Request Forms, Clinical Paks for shipping and prepaid shipping labels. To place a supply order, please call our Customer Service Staff at 800-795-5385.

Pricing
The price of the ReceptivaDxTM Assay is $690.00. This includes the BCL6 marker and a complete pathology analysis. Beta 3 Integrin and CD138 markers can be added to your ReceptivaDx Panel for an additional $125 per marker.

 

Credit card payment information must accompany the sample submission. Biopsies received by our lab without the necessary payment information will not be processed until payment is received. We accept all major credit cards. Patients that prefer to make payment by phone on or before their biopsy date can call Customer Service at 800-795-5385.

 

A detailed receipt will be provided via email once payment is received. This receipt can be used by patients to assist with reimbursement if coverage is available from their insurance carrier.

Cancellation Policy
Once the test has been received and processed by our laboratory, testing cannot be cancelled and no refunds will be made.

 

Improper Biopsy
Collection Physicians and patients are asked to pay close attention to the timing of the endometrial biopsy. Please refer to our sample collection requirements for specific data. Collection of samples outside the biopsy window will not result in a refund after the sample has been received and processed.

 

Repeat Biopsy Discount
If healthcare providers are submitting a 2nd biopsy for follow-up within 2 years of the initial ReceptivaDxTM submission, a discount of $100 will be applied. Please indicate on the test request form that a previous biopsy (provide date of service) was performed for the discount to be applied to the repeat biopsy charge.

The ReceptivaDxTM Test was developed by CiceroDx in conjunction with Pathology Consultants, Inc. of Greenville, SC. Pathology Consultants, Inc. is a laboratory certified under the Clinical Laboratory Improvement Amendments (CLIA). As with other laboratory-developed tests, this testing service has not been cleared or approved by the US FDA or any other federal regulatory agencies. Data have not been submitted to or evaluated by Federal regulatory agencies and the test is not for sale as an In Vitro Diagnostic (IVD) in the US or the EU.


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