Overview
Since 20 September 2021 self-declared 'non-commercial organisations' are no longer required to provide a lobby budget. See above timeline for this registrant's historical lobby budget.
Lobbying Costs
None declared
Financial year: Aug 2023 - Jul 2024
Lobbyists (Full time equivalent)
4.75 Fte (11)
Lobbyists with EP accreditation
0
High-level Commission meetings
1
Lobbying Costs over the years
-
Info
PETA Science Consortium International e.V. (PSCI)
EU Transparency Register
484576440734-93 First registered on 18 Dec 2020
Goals / Remit
PSCI was established in Germany (Registration Number VR 724927) as a result of the UK’s withdrawal from the EU, in order to carry forward in the EU the work of the UK-based PETA International Science Consortium Ltd. (“PISC”, registered in England and Wales as company number 08312511 and transparency register identification number 83485908659-40). The goals, activities, and structure are essentially the same as those of PISC, as set forth herein. PSCI represents the interests of its members and their individual supporters. PSCI co-ordinates its own and its members' scientific and regulatory expertise to promote reliable and relevant strategies to reduce and replace the use of animals in experiments. Building on the previous work of PISC at the EU level, PSCI provides technical support to companies and researchers seeking to replace, reduce, or refine the use of animal tests, and advises its members with regard to providing financial support to companies to achieve this goal.
Main EU files targeted
• REGULATION (EC) 1107/2009 – Placing of Plant Protection Products on the market
• REGULATION (EC) No 1907/2006: Regulation concerning the Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH)
• REGULATION (EC) No 440/2008: Regulation laying down test methods (TMR) pursuant to Regulation (EC) No 1907/2006
• REGULATION (EC) No 1272/2008: Regulation on classification, labelling and packaging (CLP) of substances and mixtures
• REGULATION (EU) No 528/2012: Regulation concerning the making available on the market and use of biocidal products
• REGULATION (EC) No 1223/2009 Regulation on cosmetic products
• REGULATION (EU) No 503/2013 on applications for authorisation of genetically modified food and feed
• DIRECTIVE 2010/63/EU: Directive on the protection of animals used for scientific purposes
• European Union Reference Laboratory for Alternatives to Animal Testing (EURL ECVAM)
• European Partnership for Alternatives Approaches to Animal Testing (EPAA)
• Organisation for Economic Co-operation and Development (OECD) Test Guidelines Programme
• OECD Adverse Outcome Pathway (AOP) development programme
• OECD programme on the safety of manufactured nanomaterialsAddress
Head Office
Friolzheimer Str. 3
Stuttgart 70499
GERMANYEU Office
Friolzheimer Str. 3
Stuttgart 70499
GERMANYWebsite
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People
Total lobbyists declared
11
Employment time Lobbyists 75% 2 50% 4 25% 5 Lobbyists (Full time equivalent)
4.75
Lobbyists with EP accreditation
No lobbyists with EP accreditations
Complementary Information
None declared
Person in charge of EU relations
Data not provided by Register Secretariat due to GDPR
Person with legal responsibility
Data not provided by Register Secretariat due to GDPR
-
Categories
Category
Non-governmental organisations, platforms and networks and similar
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Networking
Affiliation
none
Member organisations
None declared
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Financial Data
Interests represented
Does not represent commercial interests
Closed financial year
Aug 2023 - Jul 2024
Lobbying costs for closed financial year
Since 20 September 2021 self-declared 'non-commercial organisations' are no longer required to provide a lobby budget. See above timeline for this registrant's historical lobby budget.
Total organisational budget in closed year
260,850€
Major funding types in closed year
Member's contributions
Major contributions in closed year
None declared
Other financial info
None declared
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EU Structures
Groups (European Commission)
High Level Roundtable on the implementation of the Chemicals Strategy for Sustainability#E03757#https://ec.europa.eu/transparency/expert-groups-register/screen/expert-groups/consult?lang=en&groupID=3757 #MEMBER #C#Civil societyCompetent Authorities' Expert Group on the protection of animals used for scientific purposes#E02539#https://ec.europa.eu/transparency/expert-groups-register/screen/expert-groups/consult?lang=en&groupID=2539 #OBSERVER #C#OtherSub-group on GHS ATPs#E02385/5#https://ec.europa.eu/transparency/expert-groups-register/screen/expert-groups/consult?lang=en&groupID=105092 #OBSERVER #C#OtherCompetent Authorities for Registration, Evaluation, Authorisation and restriction of CHemicals (REACH) and Classification, Labelling and Packaging (CLP)#E02385#https://ec.europa.eu/transparency/expert-groups-register/screen/expert-groups/consult?lang=en&groupID=2385 #OBSERVER #C#Other
Groups (European Parliament)
N/A
Communication activities
In addition to assisting research organisations and private industries in the development of best practices, PSCI has taken over PISC’s interactions with national and international regulatory bodies and standards organisations in the EU to ensure that opportunities exist to increase and harmonise the use of validated non-animal test methods. PSCI engages with a number of regulatory bodies, including but not limited to the European Chemicals Agency (ECHA) and the European Union Reference Laboratory for alternatives to animal testing (EURL ECVAM) Stakeholder Forum (ESTAF). This engagement involves, for example, participation in expert working groups, submission of comments on regulatory initiatives and direct communication as appropriate.
An area of primary concern is the REACH (Registration, Evaluation, Authorisation and Restriction of Chemical Substances) regulation. This on-going extensive project includes working with ECHA and the European Commission regarding the use of animals as a last resort, and liaising with companies to ensure they implement validated non-animal methods.
PSCI works to minimise animal testing conducted to meet data requirements included in the biocides and plant protection products regulations.
A significant objective is to influence international testing guidelines which determine the number of animals and the exact nature of the procedures to be used in globally standardised toxicity tests. PSCI works extensively on these guidelines through the International Council on Protection of Animals in Organisation for Economic Cooperation and Development (OECD) Programmes (ICAPO), and seeks to ensure the best possible science and animal welfare (using reduction and refinement strategies) and the widest possible integration of alternatives to in vivo test methods in OECD guidelines and programmes. This work is critical to ensuring that the OECD's international test standards for human health and ecological safety use non-animal methods and approaches. When working on behalf of ICAPO, PSCI scientists represent animal protection organisations from North America, Europe, Japan and India.
PSCI and its members submit detailed scientific comments on a wide range of new test guidelines or those undergoing revision, thus influencing the development and validation of test guidelines from an early stage.
PSCI ensures that information regarding the use of non-animal tests is accessible to all audiences by publishing technical briefs and articles in peer-reviewed journals, hosting webinars and workshops and by presenting at scientific, administrative and legislative conferences.
In cases where promising in vitro techniques require additional development or validation in order to gain regulatory acceptance, PSCI advises its members to assist in providing funding.
PSCI also organises training sessions to help scientists become more proficient with in vitro and in silico methods.Other activities
None declared
Meetings
Meetings
1 meetings found. Download meetings
The list below covers meetings with Commissioners/Cabinet members/Directors-general (high-level) Commission meetings published December 2014 to December 2024, and the meetings of Commissioners/Cabinet members/Directors-general and officials holding "management functions" in the Commission published since 1 January 2025. Other lobby meetings with lower-level staff may well have taken place, but the Commission doesn't proactively publish information about these meetings. All information below comes from the Commission and not from the registrant.
1 July 2024: We have noted that some meetings are appearing in duplicate, ie. some meetings seem to be listed twice. This seems to be because the Commission changes some element of a meeting data after the meeting has first been listed, which causes LobbyFacts to register it as a new meeting. We are investigating further.