Epi Pen Training, epipen training, epi pen training Dublin, epi pen training Ireland

Did you know that your school, creche, Montessori, sports venue, company or organisation can now purchase emergency medications to hold on site for use in a medical emergency? well you can! In addition to organisations having the ability access selected medications, they can now avail of accredited training for each medication certified by the Pre-Hospital Emergency Care Council. Does your organisation have someone with a severe allergy? a diabetic? an asthmatic? maybe even the possibility of a substance overdose? if so you should consider becoming a listed organisation with the HPRA and completing the accredited training for the specific medication you require. Registration with HPRA is easy and costs just €10. Some frequently asked questions are included below and our team are at your disposal for any additional questions.

Frequently Asked Questions

1. What is the emergency medicines legislation for non-medical persons?

In October 2015 the Minister of Health signed into legislation – Statutory Instrument SI No. 449 of 2015 Medicinal Products (Prescription and Control of Supply (Amendment) (No. 2) Regulations (commonly known as SI 449 of 2015 or the emergency medicines legislation). These Regulations allow trained non-medical persons to administer six prescription–only medicines to a person, without a prescription, for the purpose of saving their life or reducing severe distress in an emergency situation. The emergency medicines are:

•    Epinephrine (adrenaline) auto-injector
•    Glucagon hydrochloride injection
•    Glyceryl trinitrate sublingual spray
•    Naloxone hydrochloride pre-filled syringe
•    Salbutamol 100mcg multi-dose inhaler
•    Medical gas mixture of 50% nitrous oxide and 50% oxygen
(Note: the administration of this is restricted to those engaged or employed by an emergency rescue organisation*)

*In the context of these Regulations, an ’emergency rescue organisation’ means an organisation whose functions include provision of rescue services to persons who cannot, without specialised assistance, remove themselves from danger or entrapment, due to injury, illness or environmental conditions.

To ensure that these medicines are administered safely, the legislation requires that the non-medical person completes an approved training course for each of the medicines that they wish to administer.

As well as completing an approved training course, the person must be engaged or employed (including in a voluntary capacity) by a listed organisation which may obtain a stock of the specified medicine for supply and administration in the event of an emergency.

The Regulations also require that the listed organisation must appoint an accountable person. This may be a person who has completed the training to administer emergency medicines, or another person.

Statutory Instrument SI No. 449 of 2015 Medicinal Products (Prescription and Control of Supply (Amendment) (No. 2) Regulations is available to read at www.irishstatutebook.ie.

2. What are the emergency medicines covered in this new legislation?

Medication Emergency Condition  Administration Route
Epinephrine (adrenaline)
(pre-filled syringe)
Treatment of anaphylactic shock (adults and children) Intramuscular injection
Glucagon Treatment of hypoglycaemia (adults and children) Intramuscular or subcutaneous injection
Glycerol trinitrate Treatment of severe angina attack (adults) Sublingual spray
Medical gas mixture of 50% nitrous oxide and 50% oxygen Pain releif in emergency rescue situations (adults and children) Inhalation
Naloxone hydrochloride
(pre-filled injection)
Treatment of respiratory depression secondary to known or suspected narcotic overdose (adults and children) Intramuscular injection
Salbutamol inhaler Treatment of acute asthmatic attack (adults and children) Inhalation

3. What is a listed organisation?

​ An organisation that wishes to procure one, or more, of the six emergency medicines must notify the Health Products Regulatory Authority (HPRA) by completing a form which can be accessed at www.hpra.ie. The organisation must notify the HPRA of the address of each premises where the medicines will be stored for use in an emergency. The HPRA will publish a list of organisations that have provided a valid notification on their website. When entered onto this list, the organisation is a “listed organisation”.

Under the Regulations an organisation can include:

a)    An organisation, body, person or group in control of a place of worship, a place of hospitality, an entertainment venue, a place of work, a sports venue, a sports club, a train station, a bus station, a ferry port, an airport or aerodrome, a commercial aircraft, a passenger ferry, a supermarket, a shopping centre, an educational establishment, a childcare facility, a crèche, a museum, an art gallery, an exhibitions centre

b)    An Garda Síochána,

c)    the Courts Service,

d)    a local authority,

e)    the Health Service Executive,

f)     a fire service,

g)    an emergency rescue organisation – defined as: “an organisation whose functions include provision of rescue services to persons who cannot, without specialised assistance, remove themselves from danger or entrapment due to injury, illness or environmental conditions”.

4. What does it mean to be the accountable person in a listed organisation?

A listed organisation must appoint one or more persons, who is employed or engaged by the listed organisation, (including in a voluntary capacity or as a volunteer) to be the accountable person(s). The accountable person is legally responsible for compliance with the Regulations, including the safe storage and use of emergency medicines by persons who have completed the approved training.

The Regulations state that the accountable person must:

•    oversee and manage the appropriate storage of a medicine procured by the listed organisation for use in an emergency
•    oversee and manage the appropriate conditions for storage of such medicine
•    ensure that the medicine is procured from a registered retail pharmacy business or where the medicine is the medical gas mixture of 50% nitrous oxide and 50% oxygen (for example Entonox) from the holder of a wholesaler’s authorisation
•    ensure that such medicine is only supplied to a person(s) (who may also be the accountable person) employed by or engaged by the listed organisation for supply and administration in an emergency
•    maintain confidential records at the premises of the listed organisation for the procurement and storage of such medicine
•    ensure that the person(s) with responsibility for supplying and administering such medicines in an emergency are appropriately trained and that their training certificate is valid
•    assist An Gard Síochána or any other investigative body with its investigations in the event of an adverse event or incident relating to the procurement, storage, supply or administration of the medicine.

5. What do I need to do to be able to administer any of these medications?

You must complete a Cardiac First Response (CFR) course in accordance with PHECC current CFR Education and Training Standards. In addition to CFR skills, you will be trained in the administration of the specific medication for the course chosen.  You will also be taught how to manage a person in the following circumstances:

a)   severe reaction (anaphylaxis) in an out-of-hospital environment,
b)   hypoglycaemia,
c)    severe angina attack,
d)   respiratory depression secondary to known or suspected narcotic overdose and
e)   acute asthmatic attack in an out-of-hospital setting until handover (or referral) to the appropriate practitioner.

* Note: The administration of Medical gas mixture of 50% nitrous oxide and 50% oxygen is directed at those training as Emergency First Responders (EFRs) and who are employed by or volunteering with an emergency rescue organisation that is listed with HPRA.

6. Where can I access a course(s)?​

Only PHECC recognised institutions (RI) approved for each course can deliver this training. Our website will list the RIs that are approved to deliver these courses and training.  DX2 is a Recognised Institution to deliver these courses, view the information here.
The courses will be available to:
•    existing and new CFR responders who wish to avail of PHECC certified additional training in any or all of the 5 medications (adrenaline auto-injector, glucagon hydrochloride injection, glyceryl trinitrate sublingual spray, naloxone hydrochloride pre-filled syringe, salbutamol multi-dose inhaler)
•    existing and new EFR responders who are practising on behalf of a listed emergency rescue organisations – for Medical gas mixture of 50% nitrous oxide and 50% oxygen only.

7. What can I expect on the Cardiac First Response course with one/or more of the medications for listed organisations?​

The CFR part of the course uses a video to guide course delivery as well as instructor and student manuals. This part of the course takes about 4-5 hours.   These courses consist of the following modules:

•    Module 1 Basic Emergency Care
•    Module 2 Access and use of an Automated External Defibrillator
•    Module 3 Safety and Communication
•    Module 4 Medication Management
•    Module 5 Medication Administration

The duration of the Medication Management – Module 4 and Medication Administration Module 5 including assessment is no less than 2-4 hours. The assessment will be skills based designed scenarios and multiple choice questions to support your knowledge and skills learned in the course.

8. Will I get a certificate?​

Yes, if you are successful in the course you will be issued with a joint PHECC/Recognised Institution CFR or EFR certificate and named medicinal product cards/certificates as appropriate.  The CFR certification lapses after 2 years when a new course must be undertaken.

The EFR certification lapses after 3 years. It is also necessary for you to retain certification in CFR (every 2 years).

9. How can I obtain these medicines for use in an emergency?​

A listed organisation can obtain emergency medicines from a pharmacy to hold as stock on their premises for use in the event of an emergency.  An order for the medicine must be presented to the pharmacy that has been signed by the accountable person taking responsibility for the medicine.

The legislation does not allow for individual persons to obtain these medicines.  The Health Product Regulatory Authority (HPRA) is the regulator responsible for establishing and maintaining the list of organisations authorised to obtain these medicines.

SI 449 of 2015 requires the listed organisation to appoint a person or persons employed or engaged by that organisation, (including volunteers) to carry out/perform certain responsibilities/functions which include safe management, storage and recording.  The person(s) appointed is called the accountable person(s).

The Eleventh Schedule of SI 449 of 2015 details what a listed organisation must provide to HPRA in order to be registered as a listed organisation and obtain the medicines for use in emergencies. The details are:

1.    Organisation name and address
2.    Name of the accountable person(s) appointed
3.    Business name or trading style to be used by the organisation where that name is different to the name required above
4.    Permanent address of the premises where your organisation is going to store the medicines and from which/where they are to be supplied
5.    Starting date for when the listed organisation is going to be holding the medications for use in emergencies.
6.    Name of the medicine(s) the listed organisation wishes to procure/obtain
7.    Declaration/statement that the procurement, storage, supply and administration of medication for use in emergencies will be conducted in compliance with the SI 449.

The HPRA has an online system for organisations – the Emergency Medicines Portal to notify HPRA of their intention to procure or purchase a specific medicine from a pharmacy or other supplier for supply and administration in the event of an emergency situation.

Our Medications for Listed Organisations Courses

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