Information related to the NCE approval of tafenoquine succinate
Dear Therapeutic Goods Administration,
The new chemical entity (NCE) 'tafenoquine succinate' has recently been approved for registration as a schedule 4 substance on the TGA Poisons Register with effect from 1 February 2018.
Regarding this pre-registration and registration application information pertaining to the registration of tafenoquine succinate, clease can you provide the following information regarding this Schedule 4 approval, and the NCE application (the registration application and pre-submission documents) from which this approval was given:
1. The number and nature of all adverse event reports a) submitted for tafenoquine to the TGA adverse events database, and b) the number and nature of those adverse event reports considered at part of the delegates application review process;
2. The detailed consumer (patient) information statements submitted a) as part of the registration application and b) those approved for tafenoquine succinate including dose rates and treatment schedules;
3. All information in the application for registration and / or pre-registration documentation relating to requirements for cytochrome P450 (CYP450) screening in patients prior to treatment with tafenoquine succinate, either for prophylaxis or treatment of malaria.
This is the second iteration of this request. I hope that your department will be able to furnish me with this information.
As this information is not for commercial use and represents a public interest inquiry, I ask that the fees associated with this process be waived.
Yours faithfully,
Dr Jane Quinn
Dear Ms Quinn
I am writing in relation to the scope of your FOI request FOI275-1718.
Can you please clarify if you are seeking 'personal information' (e.g.,
the names and/or contact details of any individuals, or any information
that could reasonable identify an individual) of third parties contained
in the documents requested?
Confirmation from you that you are not seeking personal information may
enable more timely and less costly processing of your request. For
example, consultation with identified individuals can add to the time and
cost taken to process your request.
If you are not seeking access to personal information, you can simply
reply: 'no personal information requested'.
In relation to departmental staff, we advise the standard approach is that
Commonwealth employee names and contact details below Senior Executive
Service level and mobile telephone numbers of all staff are not released.
We look forward to hearing from you by COB Friday 13 April 2018.
Kind regards
Karen
Freedom of Information
Jodie | Karen | Heather | Shreya
(02) 6232 8720
Reporting and Collaboration Services Section
Regulatory Engagement and Planning Branch
Therapeutic Goods Administration
Address: PO Box 100, Woden ACT, 2606
Email: [1][email address]
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dissemination of this communication is strictly prohibited. If you receive
this transmission in error please notify the author immediately and delete
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Dear TGA FOI,
Many thanks for your response.
I can confirm that no personal information is required.
Yours sincerely,
Jane Quinn
Attention: Jane Quinn
FREEDOM OF INFORMATION REQUEST – NOTIFICATION OF RECEIPT
I am writing to notify you that the Department of Health (Department) has received your request (in your below email) for access to documents under the Freedom of Information Act 1982 (FOI Act).
The Department will take all reasonable steps to notify you of a decision no later than 30 calendar days after the date your request was received. You will be contacted where a charge is applied for processing your request or if we need to consult a third party.
Unless you advise otherwise, duplicate documents and Commonwealth employee names and contact details below Senior Executive Service level and mobile telephone numbers of all staff will be excluded from the scope of your request under s22(1)(a)(ii) of the FOI Act.
You can contact the FOI Unit on (02) 6289 1666, or via email at [email address], should you have any enquiries.
Regards
FOI Unit
Legal Advice & Legislation Branch
Legal & Assurance Division
Australian Government Department of Health
T: (02) 6289 1666 | E: [TGA request email]
PO Box 9848, Canberra ACT 2601, Australia
The Department of Health acknowledges the traditional owners of country throughout Australia, and their continuing connection to land, sea and community. We pay our respects to them and their cultures, and to elders both past and present.
-----Original Message-----
From: Jane Quinn [mailto:[FOI #4475 email]]
Sent: Monday, 9 April 2018 10:43 AM
To: FOI
Subject: Freedom of Information request - Information related to the NCE approval of tafenoquine succinate [SEC=No Protective Marking]
Dear Therapeutic Goods Administration,
The new chemical entity (NCE) 'tafenoquine succinate' has recently been approved for registration as a schedule 4 substance on the TGA Poisons Register with effect from 1 February 2018.
Regarding this pre-registration and registration application information pertaining to the registration of tafenoquine succinate, clease can you provide the following information regarding this Schedule 4 approval, and the NCE application (the registration application and pre-submission documents) from which this approval was given:
1. The number and nature of all adverse event reports a) submitted for tafenoquine to the TGA adverse events database, and b) the number and nature of those adverse event reports considered at part of the delegates application review process;
2. The detailed consumer (patient) information statements submitted a) as part of the registration application and b) those approved for tafenoquine succinate including dose rates and treatment schedules;
3. All information in the application for registration and / or pre-registration documentation relating to requirements for cytochrome P450 (CYP450) screening in patients prior to treatment with tafenoquine succinate, either for prophylaxis or treatment of malaria.
This is the second iteration of this request. I hope that your department will be able to furnish me with this information.
As this information is not for commercial use and represents a public interest inquiry, I ask that the fees associated with this process be waived.
Yours faithfully,
Dr Jane Quinn
-------------------------------------------------------------------
Please use this email address for all replies to this request:
[FOI #4475 email]
Is [TGA request email] the wrong address for Freedom of Information requests to Therapeutic Goods Administration? If so, please contact us using this form:
https://www.righttoknow.org.au/change_re...
This request has been made by an individual using Right to Know. This message and any reply that you make will be published on the internet. More information on how Right to Know works can be found at:
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If you find this service useful as an FOI officer, please ask your web manager to link to us from your organisation's FOI page.
-------------------------------------------------------------------
______________________________________________________________________
"Important: This transmission is intended only for the use of the addressee and may contain confidential or legally privileged information. If you are not the intended recipient, you are notified that any use or dissemination of this communication is strictly prohibited. If you receive this transmission in error please notify the author immediately and delete all copies of this transmission."
Dear Dr Quinn
Please find attached correspondence in relation to your Freedom of
Information request.
As set out in the attached correspondence, we seek your response within 14
days, being 17 May 2018.
Pursuant to section 24AB(8) of the Freedom of Information Act 1982, the
statutory timeframe for processing your request is set aside during this
consultation process.
If you have any questions, please do not hesitate to contact the FOI Team.
Kind regards
Jodie
Jodie Russell | Karen Bedford | Heather Davidson | Tara Condon
HPRG Regulatory Information Access
[1]cid:image002.png@01D3B7B3.BF8638F0
Reporting & Collaboration Services| Regulatory Engagement & Planning
Health Products Regulation Group
Australian Government Department of Health
T: 02 6232 8720 | 02 6232 8772 | 02 6232 8012 | 02 6232 8826 | E:
[2][email address]
Location: Symonston, GE26
PO Box 100, Canberra ACT 2601, Australia
The Department of Health acknowledges the traditional owners of country
throughout Australia, and their continuing connection to land, sea and
community. We pay our respects to them and their cultures, and to elders
both past and present.
--------------------------------------------------------------------------
"Important: This transmission is intended only for the use of the
addressee and may contain confidential or legally privileged information.
If you are not the intended recipient, you are notified that any use or
dissemination of this communication is strictly prohibited. If you receive
this transmission in error please notify the author immediately and delete
all copies of this transmission."
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Dear Mr McDonald,
With reference to your letter of 3^rd May 2018, please can you amend my
request to include only the following parameter:
1. The number and nature of all adverse event reports a) submitted
for tafenoquine to the TGA adverse events database, and b) the number and
nature of those adverse event reports considered as part of the delegates
application review process.
I confirm again that all information can be anonymized, I do not request
any individual to be identified in this information.
I look forward to your acknowledgement of receipt of this email, and a
response to my FOI inquiry.
Kindest regards,
Jane
Associate Professor Jane Quinn
Associate Dean Research (Acting), Faculty of Science
Charles Sturt University
Boorooma Street
Wagga Wagga NSW 2701
Tel: +61 (0)2 69334208
Email: [1][email address]
[2]CSU_Logo Mark_CMYK
[3]Charles Sturt University
| ALBURY-WODONGA | BATHURST | CANBERRA | DUBBO | GOULBURN | MELBOURNE | ORANGE | PORT
MACQUARIE | SYDNEY | WAGGA WAGGA |
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Dear TGA FOI,
I have responded to the email address identified in your letter of 3 May 2018 with the information below. The date today is 11 May.
Dear Mr McDonald,
With reference to your letter of 3rd May 2018, please can you amend my request to include only the following parameter:
1. The number and nature of all adverse event reports a) submitted for tafenoquine to the TGA adverse events database, and b) the number and nature of those adverse event reports considered as part of the delegates application review process.
I confirm again that all information can be anonymized, I do not request any individual to be identified in this information.
I look forward to your acknowledgement of receipt of this email, and a response to my FOI inquiry.
Yours sincerely,
Jane Quinn
Dear Ms Quinn,
Thank you for your email of 11 May 2018.
Following further consultation with the relevant line area, we can advise that the revised scope provided by you, as outlined below, is still too voluminous for the TGA to process since the context of what documents would fall within scope has not changed significantly.
Specifically, part b of the revised scope would require manually reviewing dossiers to identify the information you have requested. As advised in our correspondence of 3 May 2018, dossiers generally contain in excess of 100,000 pages and to undertake a review of these documents would unreasonably divert the resources of department staff.
The TGA may be able to provide documents relating to part a of your revised request. We note however, information relating to Adverse Event Reports are publically available on the Database for Adverse Event Notifications (DAEN) website via the following link: https://apps.tga.gov.au/PROD/DAEN/daen-e... .
Based on the above, we would like to provide an additional opportunity for you to consider revising the scope of your request.
Please note, if you indicate that you do not wish to revise your request or you revise it in such a way that the decision maker is still of the view that processing it would substantially and unreasonably divert TGA resources, the decision maker may refuse your request under section 24(1)(b) of the FOI Act.
Pursuant to section 24AB(5) of the FOI Act, the consultation timeframe has been extended until Thursday 24 May 2018, to allow you sufficient time to consider the above.
If you have any questions, please do not hesitate to contact the FOI Team.
Kind regards,
Freedom of Information
(02) 6232 8720
Reporting and Collaboration Services Section
Regulatory Engagement and Planning Branch
Therapeutic Goods Administration
Address: PO Box 100, Woden ACT, 2606
Email: [email address]
-----Original Message-----
From: Jane Quinn [mailto:[FOI #4475 email]]
Sent: Friday, 11 May 2018 3:59 PM
To: TGA FOI
Subject: Re: FW: FOI275-1718 - Request Consultation Process [SEC=UNCLASSIFIED]
Dear TGA FOI,
I have responded to the email address identified in your letter of 3 May 2018 with the information below. The date today is 11 May.
Dear Mr McDonald,
With reference to your letter of 3rd May 2018, please can you amend my request to include only the following parameter:
1.The number and nature of all adverse event reports a) submitted for tafenoquine to the TGA adverse events database, and b) the number and nature of those adverse event reports considered as part of the delegates application review process.
I confirm again that all information can be anonymized, I do not request any individual to be identified in this information.
I look forward to your acknowledgement of receipt of this email, and a response to my FOI inquiry.
Yours sincerely,
Jane Quinn
-----Original Message-----
Dear Dr Quinn
Please find attached correspondence in relation to your Freedom of
Information request.
As set out in the attached correspondence, we seek your response within 14
days, being 17 May 2018.
Pursuant to section 24AB(8) of the Freedom of Information Act 1982, the
statutory timeframe for processing your request is set aside during this
consultation process.
If you have any questions, please do not hesitate to contact the FOI Team.
Kind regards
Freedom of Information
(02) 6232 8720
Reporting and Collaboration Services Section
Regulatory Engagement and Planning Branch
Therapeutic Goods Administration
Address: PO Box 100, Woden ACT, 2606
Email: [email address]
The Department of Health acknowledges the traditional owners of country
throughout Australia, and their continuing connection to land, sea and
community. We pay our respects to them and their cultures, and to elders
both past and present.
-------------------------------------------------------------------
Please use this email address for all replies to this request:
[FOI #4475 email]
This request has been made by an individual using Right to Know. This message and any reply that you make will be published on the internet. More information on how Right to Know works can be found at:
https://www.righttoknow.org.au/help/offi...
If you find this service useful as an FOI officer, please ask your web manager to link to us from your organisation's FOI page.
-------------------------------------------------------------------
______________________________________________________________________
"Important: This transmission is intended only for the use of the addressee and may contain confidential or legally privileged information. If you are not the intended recipient, you are notified that any use or dissemination of this communication is strictly prohibited. If you receive this transmission in error please notify the author immediately and delete all copies of this transmission."
Dear TGA FOI,
I have sent this as an email also:
With reference to your letter of 16 May,
Please can I amend my request to the following:
1. The number and nature of all adverse event reports a) submitted for tafenoquine to the TGA adverse events database.
I am sure you are that tafenqouine succinate is not readily searchable in the TGA database as this drug has only been very recently
I confirm again that all information can be anonymized, I do not request any individual to be identified in this information.
I look forward to your acknowledgement of receipt of this email, and a response to my FOI inquiry.
Yours sincerely,
Jane Quinn
Dear Mr McDonald,
With reference to your letter of 16 May,
Please can I amend my request to the following:
1. The number and nature of all adverse event reports a) submitted
for tafenoquine to the TGA adverse events database.
I am sure you are that tafenqouine succinate is not readily searchable in
the TGA database as this drug has only been very recently
I confirm again that all information can be anonymized, I do not request
any individual to be identified in this information.
I look forward to your acknowledgement of receipt of this email, and a
response to my FOI inquiry.
Yours sincerely,
Jane
From: Quinn, Jane
Sent: Friday, 11 May 2018 3:53 PM
To: '[FOI #4475 email]'
<[FOI #4475 email]>
Cc: Quinn, Jane <[email address]>
Subject: Response to letter of 3 May - FOI request 275-1718
Dear Mr McDonald,
With reference to your letter of 3^rd May 2018, please can you amend my
request to include only the following parameter:
1. The number and nature of all adverse event reports a) submitted
for tafenoquine to the TGA adverse events database, and b) the number and
nature of those adverse event reports considered as part of the delegates
application review process.
I confirm again that all information can be anonymized, I do not request
any individual to be identified in this information.
I look forward to your acknowledgement of receipt of this email, and a
response to my FOI inquiry.
Kindest regards,
Jane
Associate Professor Jane Quinn
Associate Dean Research (Acting), Faculty of Science
Charles Sturt University
Boorooma Street
Wagga Wagga NSW 2701
Tel: +61 (0)2 69334208
Email: [1][email address]
[2]CSU_Logo Mark_CMYK
References
Visible links
1. mailto:[email address]
Dear Dr Quinn
Thank you for your email of 21 May 2018.
Request consultation process for FOI 275-1718
With respect to the request consultation process that was initiated on 3
May 2018, the decision maker has considered your revised scope of 21 May
2018 and is satisfied that a practical refusal reason no longer exists. We
will therefore process your request as revised on 21 May 2018, being for
‘The number and nature of all adverse event reports submitted for
tafenoquine to the TGA adverse events database.’
Charges for FOI 275-1718
The decision maker has decided not to impose any charges for your new FOI
request of 9 April 2018.
A decision on your new request will be due to you on or before 27 May
2018.
However, we note the FOI Guidelines provide, at paragraph 3.141, that if
the last day for notifying a decision falls on a Saturday, Sunday or a
public holiday, the timeframe will expire on the first business day
following that day. Accordingly, as the due date is a Sunday and the
following day is a public holiday, a decision will be due to you on or
before Tuesday 29 May 2018.
If you have any questions, please do not hesitate to contact the FOI team.
Kind regards
Freedom of Information
(02) 6232 8720
Reporting and Collaboration Services Section
Regulatory Engagement and Planning Branch
Therapeutic Goods Administration
Address: PO Box 100, Woden ACT, 2606
Email: [1][email address]
[2]cid:image001.png@01D1D5D9.7DDEADA0
-----Original Message-----
From: Jane Quinn [mailto:[FOI #4475 email]]
Sent: Monday, 21 May 2018 10:19 AM
To: TGA FOI
Subject: RE: FW: FOI275-1718 - Request Consultation Process
[SEC=UNCLASSIFIED]
Dear TGA FOI,
I have sent this as an email also:
With reference to your letter of 16 May,
Please can I amend my request to the following:
1. The number and nature of all adverse event reports a)
submitted for tafenoquine to the TGA adverse events database.
I am sure you are that tafenqouine succinate is not readily searchable in
the TGA database as this drug has only been very recently
I confirm again that all information can be anonymized, I do not request
any individual to be identified in this information.
I look forward to your acknowledgement of receipt of this email, and a
response to my FOI inquiry.
Yours sincerely,
Jane Quinn
-----Original Message-----
Dear Ms Quinn,
Thank you for your email of 11 May 2018.
Following further consultation with the relevant line area, we can advise
that the revised scope provided by you, as outlined below, is still too
voluminous for the TGA to process since the context of what documents
would fall within scope has not changed significantly.
Specifically, part b of the revised scope would require manually reviewing
dossiers to identify the information you have requested. As advised in our
correspondence of 3 May 2018, dossiers generally contain in excess of
100,000 pages and to undertake a review of these documents would
unreasonably divert the resources of department staff.
The TGA may be able to provide documents relating to part a of your
revised request. We note however, information relating to Adverse Event
Reports are publically available on the Database for Adverse Event
Notifications (DAEN) website via the following link:
https://apps.tga.gov.au/PROD/DAEN/daen-e... .
Based on the above, we would like to provide an additional opportunity for
you to consider revising the scope of your request.
Please note, if you indicate that you do not wish to revise your request
or you revise it in such a way that the decision maker is still of the
view that processing it would substantially and unreasonably divert TGA
resources, the decision maker may refuse your request under section
24(1)(b) of the FOI Act.
Pursuant to section 24AB(5) of the FOI Act, the consultation timeframe has
been extended until Thursday 24 May 2018, to allow you sufficient time to
consider the above.
If you have any questions, please do not hesitate to contact the FOI Team.
Kind regards,
Freedom of Information
(02) 6232 8720
Reporting and Collaboration Services Section
Regulatory Engagement and Planning Branch
Therapeutic Goods Administration
Address: PO Box 100, Woden ACT, 2606
Email: [email address]
-------------------------------------------------------------------
Please use this email address for all replies to this request:
[FOI #4475 email]
This request has been made by an individual using Right to Know. This
message and any reply that you make will be published on the internet.
More information on how Right to Know works can be found at:
https://www.righttoknow.org.au/help/offi...
If you find this service useful as an FOI officer, please ask your web
manager to link to us from your organisation's FOI page.
-------------------------------------------------------------------
--------------------------------------------------------------------------
"Important: This transmission is intended only for the use of the
addressee and may contain confidential or legally privileged information.
If you are not the intended recipient, you are notified that any use or
dissemination of this communication is strictly prohibited. If you receive
this transmission in error please notify the author immediately and delete
all copies of this transmission."
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Dear TGA FOI,
Further to your message of 24 May, I did not receive a reply to my FOI request on 29 May as advised.
Please can you advise exactly when I will be furnished with a response to my request?
Yours sincerely,
Jane Quinn
Dear Dr Quinn,
The TGA has been attempting to send you a Notice of Decision in relation to your FOI request, FOI275-1718, since 29 May 2018. However, we are continually receiving a delayed receipt, indicating that your email server cannot be reached.
We’d be grateful if you could please provide an alternate email address which we can send the Notice of Decision to, or alternatively, contact the FOI Team on the below number to provide another method of contact.
Kind regards,
Freedom of Information
(02) 6232 8720
Reporting and Collaboration Services Section
Regulatory Engagement and Planning Branch
Therapeutic Goods Administration
Address: PO Box 100, Woden ACT, 2606
Email: [email address]
-----Original Message-----
From: Jane Quinn [mailto:[FOI #4475 email]]
Sent: Sunday, 3 June 2018 6:15 PM
To: TGA FOI
Subject: RE: FOI275-1718 - Request Consultation Process [SEC=UNCLASSIFIED]
Dear TGA FOI,
Further to your message of 24 May, I did not receive a reply to my FOI request on 29 May as advised.
Please can you advise exactly when I will be furnished with a response to my request?
Yours sincerely,
Jane Quinn
-----Original Message-----
Dear Dr Quinn
Thank you for your email of 21 May 2018.
Request consultation process for FOI 275-1718
With respect to the request consultation process that was initiated on 3 May 2018, the decision maker has considered your revised scope of 21 May
2018 and is satisfied that a practical refusal reason no longer exists. We will therefore process your request as revised on 21 May 2018, being for ‘The number and nature of all adverse event reports submitted for tafenoquine to the TGA adverse events database.’
Charges for FOI 275-1718
The decision maker has decided not to impose any charges for your new FOI request of 9 April 2018.
A decision on your new request will be due to you on or before 27 May 2018.
However, we note the FOI Guidelines provide, at paragraph 3.141, that if the last day for notifying a decision falls on a Saturday, Sunday or a public holiday, the timeframe will expire on the first business day following that day. Accordingly, as the due date is a Sunday and the following day is a public holiday, a decision will be due to you on or before Tuesday 29 May 2018.
If you have any questions, please do not hesitate to contact the FOI team.
Kind regards
Freedom of Information
(02) 6232 8720
Reporting and Collaboration Services Section
Regulatory Engagement and Planning Branch
Therapeutic Goods Administration
Address: PO Box 100, Woden ACT, 2606
Email: [1][email address]
[2]cid:image001.png@01D1D5D9.7DDEADA0
-------------------------------------------------------------------
Please use this email address for all replies to this request:
[FOI #4475 email]
This request has been made by an individual using Right to Know. This message and any reply that you make will be published on the internet. More information on how Right to Know works can be found at:
https://www.righttoknow.org.au/help/offi...
If you find this service useful as an FOI officer, please ask your web manager to link to us from your organisation's FOI page.
-------------------------------------------------------------------
______________________________________________________________________
"Important: This transmission is intended only for the use of the addressee and may contain confidential or legally privileged information. If you are not the intended recipient, you are notified that any use or dissemination of this communication is strictly prohibited. If you receive this transmission in error please notify the author immediately and delete all copies of this transmission."
Dear Dr Quinn
I am resending the email below as we received an email on 30 May 2018
stating that there was an issue delivering the email.
We received another email on 1 June 2018 again stating that there was an
issue delivering the email.
This is our third attempt to send you a decision for your FOI request
275-1718 that was originally sent to you on Tuesday 29 May 2018.
Kind regards
Freedom of Information
(02) 6232 8720
Reporting and Collaboration Services Section
Regulatory Engagement and Planning Branch
Therapeutic Goods Administration
Address: PO Box 100, Woden ACT, 2606
Email: [1][email address]
[2]cid:image001.png@01D1D5D9.7DDEADA0
From: TGA FOI
Sent: Tuesday, 29 May 2018 4:36 PM
To: 'Jane Quinn'
Cc: TGA FOI
Subject: FOI275-1718 - Notice of Decision [SEC=UNCLASSIFIED]
Dear Dr Quinn
Please find attached correspondence in relation to your Freedom of
Information request.
If you have any questions, please do not hesitate to contact the FOI Team.
Kind regards
Freedom of Information
(02) 6232 8720
Reporting and Collaboration Services Section
Regulatory Engagement and Planning Branch
Therapeutic Goods Administration
Address: PO Box 100, Woden ACT, 2606
Email: [3][email address]
[4]cid:image001.png@01D1D5D9.7DDEADA0
--------------------------------------------------------------------------
"Important: This transmission is intended only for the use of the
addressee and may contain confidential or legally privileged information.
If you are not the intended recipient, you are notified that any use or
dissemination of this communication is strictly prohibited. If you receive
this transmission in error please notify the author immediately and delete
all copies of this transmission."
References
Visible links
1. mailto:[email address]
3. mailto:[email address]
Dear Dr Quinn
Please find attached correspondence in relation to your Freedom of
Information request.
If you have any questions, please do not hesitate to contact the FOI Team.
Kind regards
Freedom of Information
(02) 6232 8720
Reporting and Collaboration Services Section
Regulatory Engagement and Planning Branch
Therapeutic Goods Administration
Address: PO Box 100, Woden ACT, 2606
Email: [1][email address]
[2]cid:image001.png@01D1D5D9.7DDEADA0
--------------------------------------------------------------------------
"Important: This transmission is intended only for the use of the
addressee and may contain confidential or legally privileged information.
If you are not the intended recipient, you are notified that any use or
dissemination of this communication is strictly prohibited. If you receive
this transmission in error please notify the author immediately and delete
all copies of this transmission."
References
Visible links
1. mailto:[email address]
Dear Dr Quinn
I am resending the email below as we received an email stating that there
was an issue delivering the email.
Kind regards
Freedom of Information
(02) 6232 8720
Reporting and Collaboration Services Section
Regulatory Engagement and Planning Branch
Therapeutic Goods Administration
Address: PO Box 100, Woden ACT, 2606
Email: [1][email address]
[2]cid:image001.png@01D1D5D9.7DDEADA0
From: TGA FOI
Sent: Tuesday, 29 May 2018 4:36 PM
To: 'Jane Quinn'
Cc: TGA FOI
Subject: FOI275-1718 - Notice of Decision [SEC=UNCLASSIFIED]
Dear Dr Quinn
Please find attached correspondence in relation to your Freedom of
Information request.
If you have any questions, please do not hesitate to contact the FOI Team.
Kind regards
Freedom of Information
(02) 6232 8720
Reporting and Collaboration Services Section
Regulatory Engagement and Planning Branch
Therapeutic Goods Administration
Address: PO Box 100, Woden ACT, 2606
Email: [3][email address]
[4]cid:image001.png@01D1D5D9.7DDEADA0
--------------------------------------------------------------------------
"Important: This transmission is intended only for the use of the
addressee and may contain confidential or legally privileged information.
If you are not the intended recipient, you are notified that any use or
dissemination of this communication is strictly prohibited. If you receive
this transmission in error please notify the author immediately and delete
all copies of this transmission."
References
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