PGT-COMPLETE(SM) TEST

PGT-COMPLETE(SM) TEST 2
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Advancing Standards of Care with our four in one genetic test

Our PGT-Complete test takes PGT-A beyond aneuploidy testing, to provide a new standard of care with the most clinically comprehensive insights

Availability

This product is available for sale in selected countries around the world.

PGTai

PGT-A
All the benefits of our innovative PGTai® 2.0 to improve the chances of IVF success

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Parental QC*
Provides patients reassurance that the intended egg and sperm were used, to help reduce parental anxiety of potential mix-ups

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Genetic PN check
Gives the capability to identify and rescue true 2PN embryos from morphologically identified 0, 1, and 3PN embryos, to confidently enable additional euploid embryo transfers

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Origin of aneuploidy
Supports the clinic and patient, by identifying the origin of abnormality, to guide future decisions

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” Keep up this great work! It is especially impressive with the amount of data you have. It gives great confidence to clinicians and ultimately our patients! “

Karen Sage, MSc, GC, Co-Founder, Fertility Genetics

Watch our PGT-Complete Webinar

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Reassure


You can be reassured your patients are receiving a four in one genetic test to guide better transfer decision-making.

PGT-A

Our unique AI innovation improves the odds of pregnancy and IVF success

The only test using artificial intelligence (AI) based on clinical outcome data, eliminating subjectivity, and improving accuracy. Our PGT-A provides greater confidence in robust and accurate results with two independent analyses (CNV and SNP) to check for abnormalities³

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Parental QC*

Patients are seeking reassurance of the parentage of their embryos.

Today’s IVF patient is more educated, motivated, and involved in their treatment than ever before. Patient concerns about ensuring the parentage of their embryos have been raised due to highly-publicized reports of IVF mix-ups.

The new Parental QC assessment included in the PGT-Complete analysis confirms a match** between the embryo biopsy sample and the provided parental samples. This reduces the anxiety of potential mix-ups for you and your patients.


* Parental QC is not reported in countries (e.g. UK) where it is not permitted by regulatory bodies.
**A match is defined as a genetic analysis that is consistent with a shared inheritance and familial relationship between the parental samples and the embryo biopsy sample

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Empower


Empowering your teams and your patients

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Genetic PN check

Empowering additional embryo transfers

We understand that visual inspection of correct embryo fertilization is challenging, as

  • PN may appear at slightly different times
  • PN may be faint or have already faded
  • A micro PN may be apparent
  • PN may be vertically stacked making identification difficult Our PGT-Complete test not only confirms correct embryo fertilization, it also enables testing of morphologically identified 0, 1 and 3PN embryos. This empowers your embryology team by allowing more embryos to be tested and therefore considered for transfer.

Let us provide your team with genetic information of correct embryo fertilization.

Arming your teams with the ability to identify and rescue true 2PN embryos, thus enabling additional embryo transfers.²

Origin of aneuploidy

Empowering your patients

The origin of aneuploidy feature included in our PGT-Complete analysis provides a direct assessment of gametic contribution to embryo aneuploidy, helping your patient make informed donor gamete decisions.

For patients considering donor gametes it is important to understand that not all aneuploidy is maternally derived, as often paternal contribution to aneuploidy can be overlooked.

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Simple test process

Designed with the patient in mind every step of the way

At CooperSurgical, we recognize that each sample that comes through our laboratory belongs to an individual or family with their own unique story and journey. We take a personalized approach to patient care and clinical service.

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PGT-Complete selected on test requistion form

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Embryo biopsy and parental cheek (buccal) swabs collected & shipped to CooperGenomics

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Samples analyzed and reported back to the clinic

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Genetic testing consultation is available before or after testing

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Brochures, Catalogs & Flyers

1. JBRA Assist Reprod. 2020 Apr-Jun; 24(2): 143–146. Blastocysts Derived From 0PN Oocytes: Genetic And Clinical Results

2. Buldo-Licciardi J, Large M, McCulloh D, McCaffrey C, Grifo J. Second generation artificial intelligence technology for preimplantation genetic testing (PRT) improves pregnancy outcomes in single thawed euploid embryo transfer cycles (STEET).
Presented at American Society for Reproductive Medicine on October 19, 2020. Available at: https://asrm.confex.com/asrm/2020/meetingapp.cgi/Paper/8645. Accessed Feb 18, 2022.

3. CooperGenomics, internal data on file.

Procedures

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Embryo Biopsy

The full solution for efficient and effective biopsy procedures

Want unlimited First line support?

All our USA and Europe Customers get free unlimited first line support with a service contract.

Support & Compliance

Our global team is committed to providing the highest standards of service and support.

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Batch Certificates

Use this tool to enter your batch number and download the corresponding certificate of analysis.

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Service

We offer a range of contract options to suit your needs: preventative maintenance and service, reliable access to spare parts, product training, and online handling of service requests.

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Hardware Warranty

Submit your Product Warranty Card online by completing our quick and easy form.

Get In Touch With Us

We’d love to hear from you. How can we help?