Selecting the right embryo is the single biggest lever in IVF. PGT-A removes the guesswork from that decision.
PGT-A screens your IVF embryos for chromosomal abnormalities before transfer — identifying which embryos have the correct number of chromosomes and the highest chance of implanting successfully. It is one of the most impactful additions to an IVF cycle, particularly for women over 35 or those with recurrent miscarriage. Thai clinics offer PGT-A using the same next-generation sequencing platforms found in leading US and European genetics laboratories.
Free, no-obligation — you pay the hospital directly with no markup.
PGT-A screens IVF embryos for aneuploidy — having too many or too few chromosomes — before transfer. A tiny biopsy from the outer layer of the blastocyst is analysed using next-generation sequencing to confirm the correct chromosome count across all 23 pairs. Transferring euploid (chromosomally normal) embryos improves implantation rates to 60–70% and significantly reduces miscarriage risk.
The biopsy is taken from the trophectoderm — the outer cell layer that becomes the placenta — not from the inner cell mass that develops into the baby. This means the embryo itself is not harmed. Results take one to two weeks, during which embryos are vitrified. A euploid embryo is then selected for transfer in a subsequent FET cycle.
PGT-A does not create better embryos — it identifies which ones are already chromosomally normal, so you transfer the one with the highest implantation potential.
60–70%
Higher Implantation Rates
Transferring a PGT-A-tested euploid embryo achieves implantation rates of 60–70%, compared to 40–50% without testing.
50–70%
Fraction of the Cost
PGT-A in Thailand costs roughly half the equivalent in the US or UK, making it a practical addition rather than a luxury upgrade.
Fewer Cycles
Reduced Time to Pregnancy
By avoiding transfer of aneuploid embryos, PGT-A reduces the number of unsuccessful transfer cycles — saving time, money, and emotional energy.
Lower
Reduced Miscarriage Risk
Chromosomal abnormalities cause most first-trimester miscarriages. Screening them out before transfer significantly lowers this risk.
We do not charge for our service — you pay the clinic directly with no markup. PGT-A is an add-on to your IVF cycle, quoted separately from the base treatment.
Your Quote Will Include
Prices are approximate and vary by technique, surgeon, and hospital. Your personalised quote will include a full cost breakdown.
PGT-A in Thailand costs between $2,000 and $3,600 for testing of up to eight embryos. Additional per-embryo fees apply above this number. The cost covers genetic counselling, the biopsy procedure, NGS analysis, results consultation, and a written report with recommendations.
The PGT-A fee includes genetic counselling before testing, the embryo biopsy performed by the embryology team, the genetic analysis using next-generation sequencing, a results consultation, and a comprehensive written report. If you have more than eight embryos to test, additional per-embryo fees apply. The IVF cycle itself is priced separately.
The number of embryos tested is the main variable. The base fee typically covers up to eight embryos, with additional charges per embryo above that threshold. If PGT-M (single-gene testing) is combined with PGT-A on the same biopsy, additional fees apply for the PGT-M component. The IVF cycle cost, medication, and embryo freezing are all separate line items.
Pricing varies by the complexity and scope of the procedure. Typical ranges at our partner hospitals in Thailand:
Exact pricing is confirmed after your consultation and treatment plan are finalised.
PGT-A in Thailand costs 50–70% less than equivalent testing in the US ($5,000–$9,000), Australia (A$4,400–A$8,000), and UK (£4,000–£7,000). Given the significant impact PGT-A has on per-transfer success rates and miscarriage reduction, the lower Thai pricing makes it a practical addition to any IVF cycle rather than an expensive upgrade.
PGT-A involves two distinct steps — a precise embryo biopsy and sophisticated genetic analysis. Both require specialised expertise and advanced technology.
Five to ten cells are carefully removed from the trophectoderm — the outer layer of the blastocyst that will become the placenta. This layer is biopsied rather than the inner cell mass, ensuring the embryo itself is unharmed. An experienced embryologist performs the biopsy using a precision laser and micromanipulation tools at the blastocyst stage (day five to six).
The biopsied cells are analysed using NGS technology, which reads the DNA to determine the chromosome count across all 23 pairs simultaneously. NGS is the current gold-standard platform for PGT-A, offering high accuracy and the ability to detect mosaicism — embryos with a mix of normal and abnormal cells. Results classify each embryo as euploid, aneuploid, or mosaic.
The accuracy of PGT-A depends on biopsy skill and laboratory analysis quality. Both are well-established at Thailand's leading fertility centres.
The biopsy must remove enough cells for reliable analysis without compromising the embryo. This requires a trained embryologist working under magnification with a precision laser. At experienced centres, the risk of embryo damage during biopsy is under 1%. The number of cells taken (typically five to ten) is calibrated to balance analysis accuracy against embryo safety.
Each embryo receives one of three results: euploid (normal chromosome count), aneuploid (abnormal), or mosaic (a mix of normal and abnormal cells). Mosaic results require careful interpretation — some low-level mosaic embryos may still be considered for transfer. A genetic counsellor reviews the results with you, explains the implications, and helps you make informed decisions about which embryo to transfer.
When your embryos reach blastocyst stage, the embryologist performs the trophectoderm biopsy. This is a laboratory procedure — you are not involved and there is nothing to recover from. Each embryo is vitrified immediately after biopsy to preserve quality while genetic analysis is completed.
Biopsied cells are sent for next-generation sequencing analysis. Each embryo receives a result: euploid, aneuploid, or mosaic. You can return home during this waiting period — results are delivered remotely.
Your specialist and genetic counsellor review the results with you. They explain which embryos are suitable for transfer, what the findings mean, and any implications of mosaic results. A clear written report is provided.
A euploid embryo is thawed and transferred to your prepared uterus in a subsequent FET cycle — a short visit of five to seven days. Transferring a PGT-A-screened embryo gives you the highest per-transfer chance of a healthy pregnancy.
No additional stay is needed beyond your IVF cycle. The biopsy happens during the standard embryo culture period. Results take one to two weeks, during which you can return home. You will return for a frozen embryo transfer — a separate visit of five to seven days — once results confirm a euploid embryo is available.
This is a possibility, particularly for women over 40 where aneuploidy rates are higher. If all tested embryos are aneuploid, options include another IVF cycle to produce more embryos, using donor eggs, or other treatment pathways. Knowing the result in advance prevents you from transferring embryos with very low implantation potential — saving time, money, and the emotional toll of an unsuccessful transfer.
PGT-A is most beneficial for women over 35, where aneuploidy rates increase significantly. For younger patients, the majority of embryos are likely euploid, so the added value of testing is smaller. However, PGT-A may still be worthwhile if you have a history of miscarriage, repeated transfer failure, or if you want to maximise the chance of success from a single transfer — particularly relevant for international patients who want to avoid multiple trips.
PGT-A is safe and widely used, but it is a screening tool with inherent limitations. Understanding what it can and cannot do is important for setting expectations.
PGT-A is a screening tool, not a diagnostic guarantee. A small percentage of results may be inconclusive. Genetic counselling is provided before and after testing so you fully understand the benefits, limitations, and implications of your results.
Yes. PGT-A is performed at licensed fertility clinics using the same biopsy equipment and NGS platforms found in top genetics laboratories worldwide. Our partner clinics employ experienced embryologists with documented biopsy proficiency and work with accredited genetics labs for analysis. Quality-control measures meet international standards.
PGT-A has high accuracy for detecting whole-chromosome aneuploidy — the most common cause of implantation failure and early miscarriage. However, it is not perfect. False positives (an embryo classified as aneuploid that is actually normal) and false negatives (the opposite) can occur, though both are rare. Mosaicism — where a biopsy sample contains a mix of normal and abnormal cells — adds complexity. These limitations are discussed in your genetic counselling session.
A mosaic embryo contains a mixture of chromosomally normal and abnormal cells. Mosaicism is detected in roughly 10–20% of biopsied embryos. Low-level mosaic embryos may still be considered for transfer in some circumstances, as a proportion can self-correct during development. The decision is made with genetic counselling, weighing the level and type of mosaicism against the alternative options available to you.
PGT-A quality depends on embryologist biopsy skill and the genetics laboratory performing the analysis. Both need to be strong.
Our partner clinics have in-house or closely partnered genetics laboratories equipped with NGS platforms for PGT-A analysis. Their embryologists perform trophectoderm biopsies routinely with documented low damage rates. The combination of experienced biopsy technique and reliable analysis produces consistent, actionable results.
PGT-A results require expert interpretation — particularly mosaic results. Our partner clinics provide genetic counselling from qualified professionals who explain the clinical significance of each result and help you make informed decisions. This is not a generic lab report — it is a personalised consultation.
Ask about the clinic's biopsy damage rate (should be under 1%). Confirm they use NGS technology, not older aCGH platforms. Check whether genetic counselling is included in the PGT-A package. Ask about turnaround time — one to two weeks is standard. And confirm the clinic handles mosaic results with nuance rather than blanket rejection of all mosaic embryos.
PGT-A changes the IVF equation by shifting from morphology-based embryo selection to genetics-based selection. Here is the practical impact.
Studies consistently show that transferring a PGT-A-screened euploid embryo improves implantation rates to 60–70% (versus 40–50% without testing) and significantly reduces miscarriage risk. The benefit is greatest for women over 35, where the proportion of aneuploid embryos increases with age. For women over 40, more than half of embryos may be aneuploid — without testing, these would be transferred with very low success probability.
PGT-A screens for chromosome number, not single-gene disorders (that requires PGT-M). It does not assess embryo quality in terms of mitochondrial function, metabolic activity, or other developmental factors. A euploid embryo still needs a receptive uterine environment and correct transfer timing to implant. PGT-A improves the odds — it does not guarantee success.
PGT-A fits naturally into your IVF timeline. The biopsy happens during normal embryo culture, and results arrive while you are home between visits.
The biopsy is performed on day five or six of embryo culture — within your standard IVF stay. Embryos are vitrified immediately after biopsy. You can return home while results are processed over one to two weeks. Once results confirm a euploid embryo, you return for a frozen embryo transfer — a separate visit of five to seven days.
PGT-A adds cost but can save money overall by reducing the number of unsuccessful transfers. It is most clearly beneficial for women over 35, those with recurrent miscarriage, and those who have experienced repeated implantation failure. For younger patients with multiple good-quality embryos, the added value is smaller — but the confidence of knowing you are transferring a chromosomally normal embryo may still be worthwhile.
If you carry a known genetic condition, PGT-M (testing for a specific gene) can be performed on the same biopsy as PGT-A. This screens embryos for both chromosomal abnormalities and the specific inherited condition simultaneously. The combined approach gives you the most comprehensive information about each embryo before transfer.
Everything you need to know about genetic screening of your embryos
Patient Care Director
Last reviewed: March 25, 2026
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