Pfizer Supplied Evidence of GMP for manufacturing and testing sites
Catherine Jamieson made this Official Information request to Ministry of Health
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From: Catherine Jamieson
Dear Ministry of Health,
In respect of each site within the following categories of site under each Covid-19 vaccine provisional consent, please provide the date that evidence of current GMP was provided as part of Medsafe's evaluation process:-
- finished product manufacturing sites
- active ingredient manufacturing sites
- finished product testing sites.
Yours faithfully,
Catherine Jamieson
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Kia ora Catherine,
Thank you for your request for official information. The reference number
for your request is: H2024046670
As required under the Official Information Act 1982, Manatū Hauora will
endeavour to respond to your request no later than 20 working days after
the day your request was received. If you'd like to calculate the
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Ngā mihi
OIA Services Team
[9]Ministry of Health information releases
------------------- Original Message -------------------
From: Catherine Jamieson
<[FOI #27664 email]>;
Received: Wed Jul 17 2024 14:29:14 GMT+1200 (New Zealand Standard Time)
To: OIA Requests <[email address]>; OIA <[email address]>;
Subject: Official Information request - Pfizer Supplied Evidence of GMP
for manufacturing and testing sites
Dear Ministry of Health,
In respect of each site within the following categories of site under each
Covid-19 vaccine provisional consent, please provide the date that
evidence of current GMP was provided as part of Medsafe's evaluation
process:-
- finished product manufacturing sites
- active ingredient manufacturing sites
- finished product testing sites.
Yours faithfully,
Catherine Jamieson
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From: OIA Requests
Kia ora Catherine,
Thank you for your request under the Official Information Act 1982 (the
Act) to the Ministry of Health – Manatû Hauora (the Ministry) on 17 July
2024 for information regarding the Comirnaty (Pfizer) COVID-19 vaccine.
You requested:
“In respect of each site within the following categories of site under
each Covid-19 vaccine provisional consent, please provide the date that
evidence of current GMP was provided as part of Medsafe's evaluation
process:-
- finished product manufacturing sites
- active ingredient manufacturing sites
- finished product testing sites.”
All approved manufacturing sites had current evidence or Good
Manufacturing Practice at the time of approval, please refer to Medsafe’s
product search for the approval date and current manufacturing sites. The
consent date and information on approved manufacturing sites for each
Comirnaty vaccine is publicly available at:
[1]https://www.medsafe.govt.nz/regulatory/d...
Further information is available on Medsafe’s product detail search which
can be found here: [2]https://www.medsafe.govt.nz/regulatory/D...
Ngâ mihi
OIA Services Team
Manatû Hauora | Ministry of Health
M[3]inistry of Health information releases
U[4]nite against COVID-19
****************************************************************************
Statement of confidentiality: This e-mail message and any accompanying
attachments may contain information that is IN-CONFIDENCE and subject to
legal privilege.
If you are not the intended recipient, do not read, use, disseminate,
distribute or copy this message or attachments.
If you have received this message in error, please notify the sender
immediately and delete this message.
****************************************************************************
References
Visible links
1. https://www.medsafe.govt.nz/regulatory/d...
2. https://www.medsafe.govt.nz/regulatory/D...
3. https://www.health.govt.nz/about-ministr...
4. https://covid19.govt.nz/
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