amend_renewal_app

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Application for an Amendment or Renewal to a Project

Authorisation under Scientific Animal Protection

Legislation

For details on completing this application form, please see the ‘Guide to Amendment and

Renewal Applications for Projects under Scientific Animal Protection Legislation’.

SECTION A: PURPOSE OF APPLICATION

PURPOSE OF APPLICATION

Tick the application type(s) required and enter details in the relevant section(s)below:

Renewal

Amendment

Project authorisation number:

User establishment name:

AE / P

SECTION B: PROPOSED RENEWAL DETAILS (if applicable)

PROPOSED RENEWAL

Date of expiry of current project authorisation:

Time extension sought (months):

Justification for request for time extension:

SECTION C: PROPOSED AMENDMENT (if applicable)

PROPOSED AMENDMENT

Tick all that apply and enter details in relevant section D (1-7) below:

1. Change to the project start date

2. Amendment to project manager

3. Amendment to or addition of deputy project manager(s)

4. Addition of new individuals who will be performing procedures

5. Addition of user establishment(s)/additional location(s)

6. Amendment(s) to procedure(s) including the addition of a new species/genetic strain and/or an increase in animal numbers and/or an increase in severity classification

7. Addition of new procedure(s)

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SECTION D: PROPOSED AMENDMENT DETAILS (if applicable)

D1. CHANGE TO THE PROJECT START DATE

This section should only be completed if procedures on animals have not commenced within one year of the issue date of project authorisation.

Issue date of project authorisation:

Proposed date of commencement of animal procedures:

Provide reason(s) as to why procedures on animals did not commence within one year of the issue date of project authorisation:

Provide information on how it was ensured that no alternatives to the use of live animals have been made available since the project was first authorised.

Provide information on how it was ensured that this work has not been carried out elsewhere since the project was first authorised. If this is a duplication of a previous study, justify why this duplication is necessary.

D2: AMENDMENT TO PROJECT MANAGER

Enter the details of the proposed project manager below:

Title:

First name:

Address 1:

Surname:

Address 2:

Address 3:

County:

E-mail:

Telephone:

Individual authorisation number: AE / I

If no current individual authorisation number exists, please state the date of application for an individual authorisation:

Please append CV (setting out education, training, experience and publication history). (A template

CV is available on the HPRA website if you wish to use it.)

D3: AMENDMENT TO OR ADDITION OF DEPUTY PROJECT MANAGER(S)

This section can be expanded by copying and pasting as many times as required. For multiple amendments/additions, select the entire table and copy and paste as required.

Title:

First name: Surname:

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Address 1:

Address 2:

Address 3:

County:

E-mail:

Telephone:

Individual authorisation number: AE / I

If no current individual authorisation number exists, please state the date of application for an individual authorisation:

State the reason for amendment to deputy project manager e.g. addition of an additional deputy project manager/replacement of deputy project manager stating full name and individual authorisation number of replaced person?

Please append CV, setting out education, training, experience and publication history. (A template

CV is available on the HPRA website if you wish to use it.)

D4. ADDITION OF NEW INDIVIDUALS WHO WILL BE PERFORMING PROCEDURES

FIRST NAME SURNAME INDIVIDUAL

AUTHORISATION

NUMBER

If no current individual authorisation number is held, state the date of application for an individual authorisation

D5. ADDITION OF USER ESTABLISHMENT(S)/ADDITIONAL LOCATION(S)

In the case of a collaboration, list the user establishment authorisation number of the new user establishment(s) at which project work is planned to take place:

USER ESTABLISHMENT NAME USER ESTABLISHMENT AUTHORISATION NO.

If an additional user establishment is being added please outline the reasons for the addition:

In the case of an amendment to a location other than the authorised user establishment(s) where procedures are planned to be carried out, list the additional location(s) where procedures are planned to be carried out and provide a scientific justification as to why each additional location is necessary:

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D6. AMENDMENT(S) TO PROCEDURE(S) INCLUDING THE ADDITION OF A NEW

SPECIES/GENETIC STRAIN AND/OR AN INCREASE IN ANIMAL NUMBERS AND/OR AN

INCREASE IN SEVERITY CLASSIFICATION

For multiple amendments, select the entire table and copy and paste as required.

Approved procedure (as listed in the project authorisation) being amended

Nature of amendment including details on any increase in animal numbers for this procedure

Justification for amendment

Provide details on any impact to adverse effects, severity or humane endpoints this amendment may have.

1.

2.

Adverse effects

Severity

3. Humane endpoints

Please append the currently approved project protocol with the proposed amendments highlighted in yellow or added as tracked change. The specific details for each procedure must be provided in the project protocol.

Has this amendment(s) been approved by an ethics committee?

Yes No

If ‘yes’ please provide a copy of the ethical review application and associated approval documentation from the relevant ethics committee as outlined in the guide to projects.

If ‘no’ please provide justification as to why an ethical review was not performed?

If the amendment includes the addition of a new animal species/genetic strain, please answer the questions and complete the tables below.

Have the animals to be used in this project been bred for specific use in scientific procedures:

Yes No

If ‘no’ please provide scientific justification for the reasons the animals were not specifically bred for use in procedures?

Have the animals to be used in this project been taken from the wild?

Yes No

If ‘yes’ please provide scientific justification for the reasons a wild animal is required?

Are the animals to be used in this project stray or feral animals of a domestic species?

Yes No

If ‘yes’ please provide scientific justification for the reasons a stray or feral animal of a domestic

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species is required?

Are the animals to be used in this project an endangered species?

Yes No

If ‘yes’ please provide scientific justification for the reasons an endangered species is required?

NB - if total animal numbers have increased as a result of this amendment(s) please ensure to complete Section E of this form.

Species

Life stage

Strain/breed

Genetic status

Genetic alteration (if GA)

Breeder/supplier establishment authorisation number

Country of origin*

Yes No Have any individual animal(s) proposed for use in this project been previously used in a scientific study?

If yes, describe the cumulative effect of the procedures on the animal(s)?

Number of animals to be used

* If animal(s) are sourced outside of the Republic of Ireland, please indicate the source of the animals and provide a certificate confirming authorisation and registration of the supplier establishment (as required under Directive 2010/63/EU) where animal(s) were bred / supplied in the country of origin.

D7. ADDITION OF NEW PROCEDURES

For multiple additions, select the entire table and copy and paste as required.

Procedure number

Species

Strain/breed

Life stage

Technique

Duration of procedure

Frequency of procedure

Pain-relieving methods and/or anaesthesia

Proposed severity classification

Humane endpoints

Number of animals to be used

Adverse effect(s) of procedure on animal welfare

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What is the fate of the animals at the end of the procedure?

If the fate of the animals is euthanasia, please state the method of euthanasia

Provide detailed justification as to why it is necessary to add this new procedure:

Please append the currently approved project protocol with the proposed amendments highlighted in yellow or added as tracked change. The specific details for each procedure must be provided in the project protocol.

Has this amendment(s) been approved by an ethics committee?

Yes No

If ‘yes’ please provide a copy of the ethical review application and associated approval documentation from the relevant ethics committee as outlined in the guide to projects.

If ‘no’ please provide justification as to why an ethical review was not performed?

If the amendment includes the addition of a new animal species / genetic strain, please answer the questions and complete the tables below.

Have the animals to be used in this project been bred for specific use in scientific procedures:

Yes No

If ‘no’ please provide scientific justification for the reasons the animals were not specifically bred for use in procedures?

Have the animals to be used in this project been taken from the wild?

Yes No

If ‘yes’ please provide scientific justification for the reasons a wild animal is required?

Are the animals to be used in this project stray or feral animals of a domestic species?

Yes No

If ‘yes’ please provide scientific justification for the reasons a stray or feral animal of a domestic species is required?

Are the animals to be used in this project an endangered species?

Yes No

If ‘yes’ please provide scientific justification for the reasons an endangered species is required?

Note: if total animal numbers have increased as a result of this amendment(s), please ensure to complete Section E of this form.

Species

Life stage

Strain/breed

Genetic status

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Genetic alteration (if GA)

Breeder/supplier establishment authorisation number

Country of origin*

Have any individual animal(s) proposed for use in this project been previously used in a scientific study?

If yes, describe the cumulative effect of the procedures on the animal(s)?

Number of animals to be used

Yes

No

* If animal(s) are sourced outside of the Republic of Ireland, please indicate the source of the animals and provide a certificate confirming authorisation and registration of the supplier establishment (as required under Directive 2010/63/EU) where animal(s) were bred / supplied in the country of origin.

SECTION E: TOTAL ANIMAL NUMBERS

If the amendment(s) involves an increase in animal numbers please state:

1

2

Total number of animals currently authorised for use

Amended total number of animals

SECTION F: DECLARATION AND UNDERTAKING

The declaration and undertaking below should be signed by or on behalf of the applicant i.e. by the project manager or proposed new project manager (designated pursuant to Regulation 47 of

S.I. No. 543 of 2012 as amended), who is responsible for the overall implementation of the project and its compliance with the project authorisation.

I hereby declare that:

I have been designated by the user to make this application on the user’s behalf.

The information contained in this application is true and correct.

I hereby undertake that in the event of the amendment or renewal of the project authorisation being granted:

To ensure fulfilment of the obligations arising by virtue of the terms and conditions of the project authorisation.

To ensure fulfilment of the requirements of S.I. No. 543 of 2012, including:

-

-

To submit an application for an amendment if any further substantial changes to the project are required.

To ensure that the project manager has a valid individual authorisation.

-

-

-

To ensure that, if appointed, the deputy project manager has a valid individual authorisation for the purpose of project management.

To ensure that all persons carrying out procedures under this project have a valid individual authorisation.

To ensure that all persons performing euthanasia under this project have a valid individual authorisation.

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-

-

-

-

-

-

-

To ensure the methods of euthanasia performed are in accordance with Annex IV of

Directive 2010/63/EU unless an exemption is granted by the HPRA.

To report any project deviations that have an adverse effect on animal health or welfare, and to report any changes to a severity classification that have an adverse effect on animal health or welfare to the designated veterinarian and/or the animal welfare body at the user establishment.

To keep written records of all animals used under this project authorisation for a minimum of 3 years, and to make all written records or project documentation available to the HPRA upon request or as part of an inspection.

To provide the user establishment with an end of project report for the finished project to be made available to the HPRA upon request.

To fulfil all reporting requirements including annual statistical returns to the HPRA.

To provide updates (if any) to the non-technical project summary (where relevant) to the

HPRA, which will be made publically available by the HPRA.

To comply with the requirements of S.I. No. 543 of 2012 for the care and accommodation of animals.

Signature of project manager: _________________________

Print/type name:

Date:

The declaration below should be signed by the compliance officer (designated pursuant to

Regulation 44 of S.I. No. 543 of 2012 as amended) responsible for ensuring compliance with the provisions of S.I. No. 543 of 2012 at the relevant user establishment.

I hereby declare that:

The applicant is affiliated to the user establishment referred to in section A.

I understand that if the applicant fails to uphold his/her responsibilities under S.I. No. 543 of

2012, this may have implications for the continued authorisation of the user establishment.

Signature of compliance officer: __________________________

(on behalf of breeder/supplier/user)

Print/type name:

Date:

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CHECKLIST

Amended project protocol (relevant sections only) – highlighted to identify changes

Certificate confirming authorisation and registration of breeding / supplying establishment (for animals sourced outside the Republic of Ireland)

Copy of ethical review application and associated documentation (where relevant)

Ethics approval document (where relevant)

CV (setting out education, training, experience and publication history) (where relevant)

Animal welfare body recommendation (where relevant)

Submit the completed form with attachments via CESP, or to sapsubmit@hpra.ie

or in hard copy to:

Receipts and Validation Department

Health Products Regulatory Authority

Kevin O’Malley House

Earlsfort Centre

Earlsfort Terrace

Dublin 2

Tel: + 353 1 676 4971

Fax: + 353 1 676 7836

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