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AES

AESGP

Industry association · Belgium · EU Transparency Register 99565011637-64

28
positions filed
in the 665 files tracked
22
legislative files
of 665 tracked
24
with a full position paper
attached to a submission

Counts here are a floor, never a total: they cover the 665 consultation files tracked so far (57,774 submissions, mostly 2021–26), so an organization's real filing history is larger, not smaller.

Who they are

Among the 1518 trade and business associations on this site, they rank #129 by legislative files engaged, a count of participation, not a measure of influence.

4.5
declared lobbying FTE
self-declared
€200K+
declared costs / yr (floor)
2
EP accreditations
as declared to the register
2009
in the register since

Declares membership of

  • AESGP represents its members in the Global Self-Care Federation (GSCF), which represents the views of the self-care i…
  • AESGP is in contact with all relevant organisations in its area of activity.

Self-declared to the EU Transparency Register (snapshot 14 Oct 2026).

Register category
Trade and business associations
Registered as
Association of the European Self-Care Industry (AESGP)
Head office
Brussels, Belgium

Self-declared to the EU Transparency Register (snapshot 14 Oct 2026); cost bands are floors, not audited totals. Reused under Commission Decision 2011/833/EU.

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Their record over time

AESGP filed 28 positions between 23 Apr 2020 and 28 Sept 2026, across 22 of the 665 legislative files tracked here, attaching a full position paper 24 times.

2020 · 1 filed2021 · 4 filed2022 · 4 filed2023 · 7 filed2024 · 4 filed2025 · 1 filed2026 · 7 filed

What they argued

Simplifying and reducing the burden of the rules on medical devices and in vitro diagnostic medical devices, and support of the European Medicines Agency for the expert panels on medical devices and the list of Union harmonisation legislationfiled 21 Apr 2026PDFsource

AESGP, the Association of the European Self-Care Industry, generally welcomes the European Commissions legislative proposal on simplifying and reducing the burden of the rules on medical devices aiming to improve the functioning of the current regulatory framework, notably regarding the smooth functioning of the single market for medical devices, while ensuring a high level of health protection for patients and…

Simplifying and reducing the burden of the rules on medical devices and in vitro diagnostic medical devices, and support of the European Medicines Agency for the expert panels on medical devices and the list of Union harmonisation legislationfiled 6 Oct 2025PDFsource

AESGP Feedback to the European Commissions Call for Evidence on Targeted revision of the EU rules for medical devices and in vitro diagnostics. AESGP, the Association of the European Self-Care Industry, represents the manufacturers of non-prescription medicines, food supplements, and self-care medical devices in Europe, an area also referred to as self-care or consumer healthcare products.

Packaging and packaging wastefiled 24 Apr 2023PDFsource

AESGP, the Association of the European Self-Care Industry, represents the manufacturers of non-prescription medicines, food supplements, and self-care medical devices in Europe, an area also referred to as self-care or consumer healthcare products. Please find AESGPs detailed comments in the attached file.

Medicinal products for human usefiled 19 Jul 2023PDFsource

AESGP expresses support for the Commission Proposal to revise the EU general pharmaceutical legislation. We believe this long-awaited revision will consolidate and streamline legislation which underwent multiple updates over the past 20 years. While AESGP members acknowledge the legislation's goals, we raise concerns on unintended consequences for non-prescription medicines (NPMs).

Medicinal products for human usefiled 27 Apr 2021PDFsource

A FIT PHARMACEUTICAL LEGISLATION TO BENEFIT E.U. CITIZENS AND HEALTH SYSTEMS AESGP supports a pragmatic and risk-based regulatory framework that fosters a stronger role for self-care and prevention. The current structure is overall fit for purpose although some issues may arise from divergent interpretation, disharmonised application and addition of gold plating or administrative elements.

Artificial Intelligence Actfiled 6 Aug 2021PDFsource

AESGP welcomes the European Commission’s effort to develop a European approach for artificial intelligence (AI) that promotes Europe’s innovation capacity while ensuring the creation of an ethical and trustworthy AI. If properly addressed, AI could bring tremendous benefits to the healthcare sector as a whole and some of its potential applications are already described in numerous publications.

Substantiation and communication of explicit environmental claims (Green Claims Directive)filed 20 Jul 2023PDFsource

AESGP feedback European Commission’s proposal for a Directive on substantiation and communication of explicit environmental claims (Green Claims Directive) July 2023 AESGP, the Association of the European Self-Care Industry, is interested to provide input on the public consultation concerning the published legislative proposal for a Directive on the Substantiation and Communication of Explicit Environmental Claims…

Opening of the attached position paper · the full paper is on the Commission’s record (source link above)

Classification, labelling and packaging of substances and mixturesfiled 30 Mar 2023PDFsource

The European Association of the Self-Care Industry (AESGP) expresses its full support for the overarching objectives of the Chemical Strategy for Sustainability (CSS). Furthermore, the AESGP welcomes the chance to offer feedback on the open public consultation regarding the Revision of the Regulation on Classification, Labelling, and Packaging of Substances and Mixtures (CLP).

European Health Data Spacefiled 28 Jul 2022PDFsource

Accompany enhanced data sharing with necessary (digital) literacy programs AESGP welcomes the European Commission’s proposal for a regulation on the European Health Data Space and its ambition to support innovation, take advantage of digital technology developments and deliver concrete results to improve healthcare in Europe.

European Health Data Spacefiled 3 Feb 2021PDFsource

LET THE KNOWLEDGE CONTAINED IN DATA OPEN DOORS TO THE FUTURE OF HEALTHCARE AESGP welcomes the European Commission’s Combined Evaluation Roadmap and Inception Impact Assessment on A European Health Data Space and its ambition to introduce innovation, to take advantage of digital technology developments and to deliver concrete results to improve healthcare in Europe.

Sustainability criteria for plastic recycling technologiesfiled 16 Sept 2026PDFsource

As the European association representing manufacturers of self-care products, including non-prescription medicines, medical devices, and food supplements, AESGP supports the main objectives of the Packaging and Packaging Waste Regulation (PPWR) to promote circularity and contribute to a more resource-efficient packaging system across the European Union.

Rules for the calculation and verification of recycled content in plastic packagingfiled 16 Sept 2026PDFsource

As the European association representing manufacturers of self-care products, including non-prescription medicines, medical devices, and food supplements, AESGP supports the main objectives of the Packaging and Packaging Waste Regulation (PPWR) to promote circularity and contribute to a more resource-efficient packaging system across the European Union.

Urban wastewater treatment. Recastfiled 14 Mar 2023PDFsource

AESGP welcomes the opportunity to submit feedback to the UWWTD proposal, due to direct impact on pharmaceutical industry, by including an Extended Producer Responsibility (EPR) scheme to finance the establishment of quaternary treatment in UWWTPs to deal with contaminants of emergent concern (CEC).

Conditions for importing recycled materials into the EU for use in packagingfiled 16 Sept 2026PDFsource

As the European association representing manufacturers of self-care products, including non-prescription medicines, medical devices, and food supplements, AESGP supports the main objectives of the Packaging and Packaging Waste Regulation (PPWR) to promote circularity and contribute to a more resource-efficient packaging system across the European Union.

Common data platform on chemicals, establishing a monitoring and outlook framework for chemicalsfiled 3 Apr 2024PDFsource

AESGP, the Association of the European Self-Care Industry, is a non-profit organisation that represents the manufacturers of non-prescription medicines, food supplements, and self-care medical devices in Europe, an area also referred to as self-care or consumer healthcare products, takes the opportunity to share its views on the One Substance, One Assessment (OSOA) package of legislative proposals published on 7…

Re-attribution of scientific and technical tasks and improving cooperation among Union agencies in the area of chemicalsfiled 3 Apr 2024PDFsource

AESGP, the Association of the European Self-Care Industry, is a non-profit organisation that represents the manufacturers of non-prescription medicines, food supplements, and self-care medical devices in Europe, an area also referred to as self-care or consumer healthcare products, takes the opportunity to share its views on the One Substance, One Assessment (OSOA) package of legislative proposals published on 7…

Re-attribution of scientific and technical tasks and improving cooperation among Union agencies in the area of chemicalsfiled 3 Apr 2024PDFsource

AESGP, the Association of the European Self-Care Industry, is a non-profit organisation that represents the manufacturers of non-prescription medicines, food supplements, and self-care medical devices in Europe, an area also referred to as self-care or consumer healthcare products, takes the opportunity to share its views on the One Substance, One Assessment (OSOA) package of legislative proposals published on 7…

Re-attribution of scientific and technical tasks and improving cooperation among Union agencies in the area of chemicalsfiled 12 Apr 2022PDFsource

AESGP welcomes the consultation initiative and the stakeholder engagement on the principle of ‘One Substance – One Assessment’ as part of the commitment in the ‘European Green Deal’. It is essential for AESGP that the implementation of the ‘One Substance - One Assessment’ (OSOA) concept which aims to reduce the administrative burden, duplication of efforts and to optimize resources does not have a negative impact on…

European Chemicals Agency and amending regulationsfiled 10 Oct 2022source

AESGP, the Association of the European Self-Care Industry, represents the manufacturers of non-prescription medicines, food supplements, and self-care medical devices in Europe, an area also referred to as “self-care” or “consumer healthcare” products. AESGP welcome the opportunity to provide our feedback on the foreseen proposal for a founding regulation of the European Chemicals Agency (ECHA).

Protection of groundwater against pollution and environmental quality standards in the field of water policyfiled 14 Mar 2023PDFsource

The Association of the European Self-Care Industry (AESGP) along with the European Federation of Pharmaceutical Industries and Associations (EFPIA) and Medicines for Europe (MfE) note positive aspects in the revision of the Directive 2000/60/EC establishing a framework for Community action in the field of water policy, Directive 2006/118/EC on the protection of groundwater against pollution and deterioration and the…

European Health Data Space HealthData@EU requirementsfiled 28 Sept 2026source

AESGP welcomes the proposed technical framework for HealthData@EU and would like to highlight three aspects that are critical for the long-term value, interoperability and scientific utility of the European Health Data Space. 1. Future-proof metadata standards and capture of OTC medicines Metadata requirements should be designed to support future use cases and evolving research needs.

European Health Data Space Board operationsfiled 5 Jan 2026source

AESGP welcomes the opportunity to comment on the draft Commission Implementing Act laying down the measures for the establishment and operation of the European Health Data Space (EHDS) Board. AESGP expresses its support for the establishment of the EHDS Board, recognizing it as a fundamental component for achieving a successful and harmonised implementation of the EHDS.

Evaluation of the European Food Safety Authority (EFSA) 2017-2024filed 8 Apr 2024PDFsource

AESGP, the Association of the European Self-Care Industry, welcomes the opportunity to provide feedback on the performance of the European Food Safety Authority (EFSA) as part of its evaluation for the period 2017-2024. You will find our feedback attached. We thank you in advance for your consideration.

European Medicines Agencyfiled 2 Feb 2021PDFsource

The Association of the European Self-Care Industry (AESGP), representing the European manufactures of consumer healthcare products (including non-prescription medicines and selfcare medical devices), would like to use the opportunity provided by the Commission to comment on the draft Regulation on a reinforced role for the European Medicines Agency in crisis preparedness and management for medicinal products and…

Fees and charges payable to the European Medicines Agencyfiled 7 Feb 2023PDFsource

Please see below the AESGP comments on the European Commission proposal on updating the rules on fees payable to the European Medicines Agency. The detailed comments are provided in the attached document. The EMA is currently funded at 86% by fees, 13% by EU contribution and 1% by other sources.

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Turns up on the same files

Organizations that also filed on at least two of the same consultations. A shared interest in the same dossiers, not evidence of coordination, and we do not suggest any.

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Quotes are verbatim from submissions published by the European Commission, trimmed to their opening passage and never summarized by a model. Organizations only, never individuals. Reused under Commission Decision 2011/833/EU; the European Commission is not liable for this reuse.