SPECTARIS Deutscher Industrieverband für Optik, Photonik, Analysen- und Medizintechnik e.V.

SPECTARIS · Trade and business associations · DE

Kategorija
Trade and business associations
Būstinė
Berlin DE
Registruota
2012-08-17
Deklaruotos metinės išlaidos
25 000–49 999 € (pačios deklaruota)
Svetainė
http://www.spectaris.de
Skaidrumo registras
55587639351-53 ↗
9
Susitikimai su EK
2
Pateiktos pozicijos
0
Pozicijos dokumentai
0
Paminėjimai spaudoje
Sumą deklaruoja pati organizacija Skaidrumo registre; institucijos jos netikrina.

Susitikimai pagal metus

2025720262

Šaltinis: Europos Komisijos skelbiami susitikimai, sutapatinti pagal skaidrumo registro numerį. n = 9 susitikimų; x — metai pagal susitikimo datą, y — susitikimų skaičius.

Susitikimai su Europos Komisija

Skelbiami tik susitikimai su Komisijos nariais, jų kabinetais ir generaliniais direktoriais. Susitikimai žemesniu lygiu ir daugelis kontaktų Parlamente bei Taryboje į registrą nepatenka.
DataPriėmėTema
2026-09-14Cabinet of Commissioner Jessika RoswallPFAS: emissions from fluoropolymers
2026-09-14Cabinet of Commissioner Jessika RoswallPFAS: emissions from fluoropolymers
2025-12-15Cabinet of Commissioner Jessika RoswallUpcoming PFAS restriction
2025-12-15Cabinet of Commissioner Jessika RoswallUpcoming PFAS restriction
2025-11-18Cabinet of Commissioner Olivér VárhelyiMedical device review
2025-11-18Cabinet of Commissioner Olivér VárhelyiMedical device review
2025-11-18Cabinet of Commissioner Olivér VárhelyiMedical device review
2025-11-04Cabinet of Executive Vice-President Stéphane SéjournéUniversal PFAS restriction under REACH
2025-11-04Cabinet of Executive Vice-President Stéphane SéjournéUniversal PFAS restriction under REACH

Ką pateikė viešoms konsultacijoms

2026-09-10 · Implementing rules on registering in and reporting to the register of producers ↗ originalus šaltinis
Please find our feedback attached as a PDF file.
2021-07-16 · Mid-term evaluation of the Union Customs Code ↗ originalus šaltinis
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Kokias ES temas nurodo sekanti

Medical Device Regulation
In Vitro Diagnostica Regulation
European Health Data Space
Standardisation / LADS (work towards an open standard for analytical and laboratory equipment)
Use of electronic instructions for use (eIFU)
Environmental and sustainabilty law (such as but not limited to REACH, RoHS, CLP, BPR, Batteries, Green Deal, CSS, PFAS, Safe and Sustainability by Design, Eco-Design, WEEE, Waste Frame Directive, Packaging and Packaging Waste, eIFU)
F-Gases Regulation
Cybersecurity and Cyber Resiliance Act
Artificial Intelligence Regulation
Digital topics such as European Health Data Space, EU Data Act
New Legislative Framework (such as but not limited to Machinery, low voltage, RED, Blue Guide)
Product liability