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About Eurofins Clinical Genetics Ireland Limited

Eurofins Clinical Genetics Ireland is a state-of-the-art, next-generation sequencing laboratory in Dublin. This laboratory offers advanced clinical genetics services, while maintaining a strong focus on advancing clinical research in our dedicated research and development laboratory at our Dublin site. This combination of entrepreneurship and intellectual academia via our University Partner, allows Eurofins Clinical Genetics Ireland to bring predictive medicine to the Irish population.

Locations

Dublin

Laboratory

TTMI, St. James' Hospital,Dublin, Campus, Dublin 8, Ireland

Laboratory

+353 (0) 1 295 8545

genetics@ctie.eurofinseu.com

Pre-analytics

Hatch Opening Hours

Monday - Friday: 8am - 4pm | Saturday: 8am - 4pm | Sunday and Public Holidays: Closed

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Samples for Eurofins Clinical Genetics Ireland are received by the Pre‑Analytics department in Blackthorn Road, Sandyford (Eurofins Biomnis Ireland) and then forwarded to our Eurofins Clinical Genetics laboratory in the UK.

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The vast majority of erroneous results are caused by errors made during sample collection and transport, rather than analytical errors within the laboratory. For this reason, it is essential that correct procedures are followed for patient preparation, sample collection, sample preparation, and sample transport. The following procedures should always be followed.

1. Patient identification

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We require at least two identifiers for every patient, both on the request form and on each sample tube. A minimum of the following are required: surname and given name, date of birth. If these are not present, the samples cannot be processed.

2. Sample collection: Maternal Peripheral Whole Blood

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  • Eurofins Clinical Genetics Ireland provide a sample collection kit specifically for NIPT (Prenatalsafe®).
  • To order this kit, please email orders@ctie.eurofinseu.com.
  • NB: Only Streck tubes may be used for the collection of whole blood for NIPT.
  • Carefully remove the Prenatalsafe® sleeve and open the box to retrieve the components required for blood collection.
  • Write the ‘Blood Draw Date’ in the designated field on the patient Request & Consent Form.
  • Write the patient first name, surname, and date of birth in the fields provided on the Streck tube label.
  • Apply a tourniquet approximately 6 cm above the selected venipuncture site (must not exceed one minute of use) and cleanse the area with an alcohol wipe.
  • Remove the plastic cover from the rubber-protected needle and attach the end of the butterfly to the vacutainer by gently twisting.
  • Insert the butterfly needle into the patient’s vein.
  • Once there is a flashback of blood, insert the Streck tube into the green attachment.
  • Collect approximately 10 mL (minimum 8 mL) of peripheral blood into the Streck tube. Do not fill the Streck tube completely, as a full tube may lead to improper insertion of the tube stopper.
  • Release the tourniquet prior to removing the needle. Place a cleansing wipe over the puncture site while removing the needle and then press it firmly on the puncture site before applying a plaster.
  • Gently invert the Streck tube 10 times.
  • Dispose of used material in accordance with local clinical waste procedures.

Samples with inadequate volume or that are sent in non-validated or expired tubes will be rejected.

3. Buccal Swabs

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Eurofins Biomnis provide a Buccal Swab kit. To order this kit, please email orders@ctie.eurofinseu.com.

  • For Prentalsafe® COMPLETE, Prentalsafe® COMPLETE Plus, and Prenatalsafe® Full Risk samples, ensure the biological father’s information is written on both the Buccal Swab tube and the Request & Consent Form.
  • Write the date of sample collection on the Buccal Swab tube.
  • Remove the lid from the Buccal Swab tube and use the swab end to firmly scrape both inner cheeks of the father.
  • Firmly recap the tube and place it in the specimen holder slot.

Samples with inadequate volume or that are sent in non-validated or expired tubes will be rejected.

4. Packaging & Shipping:

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Streck tubes and Buccal Swabs are to be stored at room temperature or refrigerated at 2-8°C until shipment. Samples should be shipped between 4°C and 30°C.

Do not keep Streck tubes in the freezer. Samples must be sent to the laboratory using the transport container provided, assembled to UN 3373 standards. Following blood draw, samples should be shipped as soon as possible.

Please follow the instructions below for packaging and shipping the samples:

  • Place the Streck tube (containing the maternal whole blood) and Buccal Swab (if relevant) in the specimen holder slots.
  • Place the patient Request & Consent Form and the specimen holder into the Prenatalsafe® box.
  • Retrieve the provided security seals from the box, close the box, replace the Prenatalsafe® sleeve on the box, and apply one security seal to each of the two short sides of the box. Ensure each seal covers both the sleeve and the box.
  • Organise sample collection:

Driver pickup: Email Eurofins Lablink on logistics@ctie.eurofinseu.com to schedule a collection by a Eurofins driver.

Samples must arrive at the laboratory within five days from blood draw for a validated result.

Opening Hours

Eurofins, Blackthorn Road Site Sample Reception

Public Opening Hours:
Monday to Sunday: 8.30am - 5.30pm

Unit 3, Sandyford Business Centre, Sandyford Business Park, Blackthorn Road, Dublin 18,D18 E528,Ireland

Eurofins Lablink

Tel: 1800 252 967
Email: lablinklogistics@ctie.eurofinseu.com

Eurofins Client Services

Public Opening Hours:
Monday to Friday: 8.30am - 5.30pm
Tel: 1800 252 966
‍Email: clientservices@ctie.eurofinseu.com

Non-Invasive Prenatal Testing (NIPT)

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Prenatalsafe® detects aneuploidy, structural chromosomal abnormalities and genetic diseases

 

We currently offer Prenatalsafe® 3 & 5. 

Prenatalsafe® is the most technologically advanced non-invasive prenatal test currently available

By analysing the cell-free fetal DNA (cffDNA) circulating in the mother’s blood, this new non-invasive prenatal test can screen for chromosomal aneuploidies and or serious genetic disease of the developing fetus.

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Who is it for?

Any expectant mother, single or twin pregnancies, conceived either through natural conception or medically assisted reproductive technologies, whether autologous or heterologous.

Reporting times: 3-5 days

PNS3 is available for singleton and twin pregnancies.
PNS5 only available for singleton pregancies.
Fetal sex determination in twin pregnancies only detects presence or absence of Y chromosome.

What is Prenatalsafe®?

Prenatalsafe® is a non-invasive prenatal test (NIPT) designed to detect the presence of chromosomal errors and genetic diseases in the developing fetus during early pregnancy (from 10 weeks). The tests are non-invasive and are performed on a simple blood sample from the mother, thus minimising risk to the fetus. The tests analyse fetal genetic material that occurs naturally in the mother’s blood during pregnancy.


Why take this test?

Unfortunately, the prevention of chromosomal abnormalities during pregnancy is impossible. NIPT for the detection of chromosomal and genetic errors make it possible for prospective parents to receive information about the health of their baby as soon as possible. This enables them along with their clinician to make informed decisions about crucial medical management, their pregnancy, and the future of their family.


How do I order this test?

Speak to your doctor, midwife, or consultant if you are interested in any of the NIPT options provided by Eurofins Clinical Genetics Ireland. Your healthcare provider will be sent your results and advise you on the next steps.

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How does it work?

During pregnancy, some fragments of the baby's DNA circulate in the mother's blood. Fetal DNA is detectable starting from the 5th week of gestation. Its concentration increases through gestation and disappears immediately after delivery.

The quantity of fetal DNA circulating from the 10th week of gestation is sufficient to guarantee the high specificity and sensitivity of the test. The test is performed on a blood sample from the mother with a gestational age of at least 10 weeks.

Through a specialised laboratory process, the cell-free circulating fetal DNA is isolated from the plasma of the maternal blood sample.

Subsequently, the entire fetal genome (cfDNA) is sequenced, using the innovative massive parallel sequencing (MPS) / Next Generation Sequencing (NGS) platforms from ILLUMINA.

The chromosomal DNA sequences are finally analysed by a bioinformatics tool to determine the presence of any fetal chromosomal aneuploidies or structural abnormalities.

Prenatalsafe® is useful in case of:

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Single pregnancies

Conceived through natural conception or assisted reproductive techniques.

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Twin pregnancies

Conceived through natural conception or assisted reproductive techniques.

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Previous Miscarriage

Pregnancies ended in miscarriage or voluntary termination.

To Learn more about commercially available methods for NIPT

Open an Account

If you are looking to open an account with Eurofins Clinical Genetics, please make sure to download both Part 1 and Part 2 of the forms below. Both forms need to be fully filled out and emailed back to marketing@ctie.eurofinseu.com to begin the onboarding process.

Contact Us

Contact Eurofins Clinical Genetics

Client Feedback

Customer Feedback - Please let us know how we are doing.

Please choose all relevant options below

Eurofins Complaints Policy & Contact Form

Please fill out this form in order to log your issue with our team. A member of the team will be in touch to help you as soon as possible.

Eurofins Biomnis / Eurofins Pathology / Eurofins Clinical Genetics / Eurofins Lablink is committed to providing a high quality laboratory service and it is our policy to continually monitor and improve the level of service afforded to our users. We encourage feedback and suggestions from our users both positive and negative. If a user encounters problems with the services provided or have suggestions for improvement, please contact your account manager or our client Services department clientservices@ctie.eurofins.eu.com A complaint may be submitted in writing, with sufficient detail and information to enable the complaint to be substantiated on receipt. Complaints will be acknowledged within 5 working days of receipt. Complaints are treated as confidential and will be investigated by the departments involved. Complaints form part of our Quality Management System and are thoroughly investigated for the root cause. Once the root cause has been identified, the appropriate corrective actions will be implemented. Follow up actions to resolve the complaint will be completed within 30 days (this is dependent on the complexity and extent of the complaint).

Accreditation

Our company's policy is to continuously assess and enhance the quality of service provided to our customers. Our Quality Management Department continuously monitor our policies and procedures, which is crucial in making sure every department operates to the necessary standard. As of June 2025 Eurofins Clinical Genetics was awarded ISO 15189:2022 accreditation, a testament to the hard work and determination of the entire team. To view the certificate or scope of accreditation please follow the link below:

 

INAB Accreditation

Privacy Notice & Open Disclosure

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Thank you for visiting our website. Please read below for full details.

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Open Disclosure

Communication to patients\doctors:

In keeping with the Patient Safety (Notifiable Incidents and Open Disclosure) Act 2023, it is the policy of Eurofins Biomnis that requesting clinicians and patients are communicated with in an open, honest, transparent and empathetic  manner following a patient safety or notifiable incident; that they are provided with a sincere and meaningful apology, especially when they are harmed as a result of such incidents; and that this communication process is initiated in a timely manner. Open disclosure is a feature of high-quality health care, and is an important contributor to patient safety.

Privacy Notice

This Privacy Notice is intended to assist you in making informed decisions when using the website and our services and/or to understand how your personal information may be processed by us as a result of providing the services or when you apply to work at Eurofins Biomnis / Eurofins Pathology / Eurofins Lablink, Eurofins Clinical Genetics, (“Eurofins”). Please take a moment to read and understand it. This privacy notice should be read in conjunction with our Cookies Notice.

Cookie Notice.
Eurofins Data Protection Officer

Email: DPO@CTIE.eurofinseu.com 

Please note: Where the laboratory is required by law or authorised by contractual arrangements to release confidential information, the original requestor will be notified of the information to be released, unless prohibited by law. This applies in particular to the notification of infectious diseases.  We are obliged by law to notify cases of notifiable diseases to Public Health. Such notification includes the diagnosis, patient name and date of birth, and patient address. https://www.hpsc.ie/notifiablediseases/notifyinginfectiousdiseases/  

DATA CONTROLLER & DATA PROCESSOR INFORMATION

Eurofins Biomnis Ireland Limited, Eurofins Pathology, Eurofins Lablink, Eurofins Clinical Genetics

("Eurofins");

Address: Three Rock Road, Sandyford Business Estate, Dublin 18, D18 A4C0, Ireland

NOTE:

Eurofins is both a Data Controller and a Data Processor, with different obligations.

As a Data Controller, we process data, for example for our employees and/or prospective
candidates that may apply to advertised positions with Eurofins and/or individuals that

contact us regarding our services.

As a Data Processor, we process data on behalf of our Clients (‘Data Controllers’),
including healthcare professionals (Doctors/GPs/Consultants/Hospitals) involving patient

data. Should a ‘Data Subject Access Request (DSAR)’ be made to Eurofins as a Data

Processor by a Patient and/or by someone representing a Patient, then the Client must be

notified of such request in compliance with data protection legislation and regulation, as the

Client is responsible to engage directly with the patient and address the Patient’ DSAR

request.

The Client decides as to whether such health data / information is to be disclosed to a Patient. Eurofins does not disclose processed health data / health information directly to a Patient.

WHAT PERSONAL INFORMATION DO WE COLLECT AND HOW?

We collect the personal information through your completion of the ‘Web-Form’ Contact Us - and/or when you submit information to us by other means (e.g. electronic email, facsimile, post).

When you use the Web-Form, such personal information usually consists of:

  • data about your identity such as your last name, your first name.
  • data about the name of your company / organisation.
  • information on how to contact you such as your e-mail address and phone number.
  • data about your query. 

The purpose of the web-form is for queries you have. We will then reply and contact you by email or phone in response to provide more information regarding your specific enquiry. You should only give us the personal information requested in the web-form and if you do not agree to provide us with this information, you must not fill in the web form.

Information that is provided by you through other means will be assessed, processed and responded to.

WHY DO WE USE PERSONAL INFORMATION ABOUT YOU?

We will use the information we collect through the web-form for the following purposes:

  • To contact you.
  • Provide, administer and communicate with you
  • Process, evaluate and respond to your requests and enquiries
  • Administer and communicate with you about your query regarding our business services
  • Provide investor and client / customer services. 

Depending on your business relationship you have with us and/or your type of query we may process the following types of data:

  • To verify your identity
  • To deliver our services
  • To improve, develop and market new services.
  • To carry out requests made by you on the website web-form in relation to our services
  • To investigate or manage complaints.
  • To comply with any applicable law, or the requirements of a regulator
  • For recruitment purposes 

To undertake these as listed above we may process the following personal information:

If you are a visitor to the website and use the web-form:

  • Name and job title.
  • Contact information including the company you work for, email address and social media account where appropriate
  • Information such as your IP address, your preferences, and interests in our business.
  • Other information relevant to the provision of Services.

If you are a client in receipt of our Services or prospective individual / client:

  • Name and job title.
  • Contact information including the company you work for and email address, where provided. o
  • Payment information for use of our services.
  • Information that you provide to us as part of us providing the services to you, which depends on the nature of your instructions to Eurofins.
  • Information you provide to us for the purposes of attending meetings and events.
  • Other information relevant to provision of our Services.

If you are a potential recruit to join Eurofins:

  • Name and job title.
  • Contact information including email address.
  • Curriculum vitae, your education, employment history and similar matters and similar information that you may provide to us.
  • Other information relevant to potential recruitment with Eurofins

WHICH PROCESSING GROUND(S) DO WE RELY UPON FOR PROCESSING YOUR PERSONAL INFORMATION?

Where we process personal data you provide, our legal basis in compliance with GDPR, for processing will vary depending on the circumstances. Ordinarily, the relevant legal basis is that the processing is:

  • necessary for performing and/or to enter into a contract.
  • necessary to comply with a legal obligation.
  • for legitimate interests you have with our company.
  • with your consent (which you may withdraw at any time)
     
    In order to process your personal data, depending on the situation, we rely on:
  • the legitimate interests you have with our company by you using the web-form and/or website
  • the legitimate interests you have with Eurofins and to reply to your query and enquires.
  • recruiting of candidates to fill our present or future job vacancies within one of the companies of the Eurofins group.
  • prevention of fraud.
  • direct marketing.
  • the necessity for the establishment, exercise or defence of legal claims.
  • transfer of information within the group for administrative and/or referral purposes.
  • maintenance (including but not limited to system fixes) of our database.
  • legal obligations
  • contract performance, including the continuous improvement of the services provided under such contracts.
  • your consent.
     
    In order to process special category data, depending on the situation, we lawfully rely on:

Processing is necessary for the purposes of preventive or occupational medicine, for the assessment of the working capacity of the employee, the provision of health (i.e. testing of samples provided to us by healthcare professionals on behalf of their patients) or for the management of our healthcare systems and services on the basis pursuant to contracts with a healthcare professionals (e.g. hospitals / GP Doctors).

In order to process personal data, we lawfully rely on at least one of the following GDPR regulatory requirements:

the data subject has given consent to the processing of his or her personal data for one or more specific purposes;
processing is necessary for the performance of a contract to which the data subject is party or in order to take steps at the request of the data subject prior to entering into a contract;
processing is necessary for compliance with a legal obligation to which the data controller / data processor is subject;
processing is necessary for the purposes of legitimate interests 

WILL YOUR PERSONAL INFORMATION BE TRANSFERRED OUTSIDE THE EUROPEAN UNION?

Transfers are subject to appropriate safeguards in compliance with GDPR Article 46. Approved standard contractual clauses (together with equivalent terms required by other relevant/applicable laws) are to ensure we will comply with our legal and regulatory obligations in relation to personal information, including having a lawful basis for transferring personal information outside of EU and putting appropriate safeguards in place to ensure an adequate level of protection for the personal information.

Your personal data might be transferred outside the EU/EEA only to countries for which:

  • the European Commission has issued an adequacy decision (which guarantees that an adequate level of protection of personal data is offered in that country).
  • Or you have given explicit consent.
  • appropriate safeguards have been provided, such as standard contractual data protection clauses. 

WHICH RIGHTS DO YOU HAVE OVER YOUR PERSONAL INFORMATION?

You have the following rights in relation to the personal data we hold for you:

  • the right to be informed about the data we hold for you and what we do with it.
  • the right for any inaccuracies in the data we hold for you, however they come to light, to be corrected. This is also known as ‘rectification.’
  • the right to have data deleted in certain circumstances. This is also known as ‘erasure.’
  • the right to restrict the processing of the data.
  • the right to transfer the data we hold for you to another party. This is also known as ‘portability.’
  • the right to object to the processing of your data.
  • the right to regulate any automated decision-making and profiling of personal data.

You also have the right to complain to the relevant national data protection authority in case these rights are not complied with. An overview of the national data protection authorities is available at the following link https://www.edpb.europa.eu/about-edpb/about-edpb/members_en 

HOW LONG WILL WE KEEP YOUR DATA FOR?

Your personal data will be stored for a limited period of time, determined with regards to the necessity, and to serve the purposes for which data has been collected and processed. Also, please note that some data retention periods are set by other statute laws (legislation) and/or regulations, depending on the type of data processed (e.g. such as information needed for income tax and audit purposes, or information on aspects of health and safety, and/or information to defend litigation issues etc.).

Any queries you may have, should be sent by email to:

Eurofins Data Protection Officer 
Email: DPO@CTIE.eurofinseu.com