欧盟农药登记合规代理EU Pesticide Registration Agent

中国农化企业进入欧盟的登记通道Your Gateway into the European Union

我们只做一件事:把中国农药原药与制剂送进欧盟 27 国市场。欧盟总部设在保加利亚普罗夫迪夫,作为欧盟境内的登记持证与法定代理主体;配合覆盖 24 个成员国的制剂登记数据与 421 个已批准活性物质动态库,从可行性初筛到拿证续展,每一步都可查、可分阶段交付。We do one thing: get Chinese pesticide active ingredients and formulations into all 27 EU member states. Our EU headquarters in Plovdiv, Bulgaria acts as the in-country certificate holder and legal agent, backed by formulation records from 24 member states and a live database of 421 approved active substances — from feasibility screening to certificate renewal, every step traceable and delivered in phases.

27
欧盟成员国覆盖EU Member States
24
国有制剂登记数据States with Formulation Data
421
欧盟已批准活性物质Approved Active Substances
分阶段
预付·可控交付Phased Delivery
服务能力Capabilities

我们能为您做什么What We Do

从首次可行性评估到取得登记证,提供端到端的代理与合规支持。End-to-end agency and compliance support — from the first feasibility check to the certificate in hand.

🌿

原药登记 / 等同性评估Active-Ingredient & TE

新有效成分登记、原药来源等同性评估(Test of Equivalence)与卷宗撰写。New active-ingredient registration, source equivalence (TE) and dossier authoring.

🧪

制剂登记Formulation Registration

终端制剂产品在各国主管机构的登记提交与跟进。End-use product registration and follow-up with national authorities.

📑

资料撰写与 GLP 对接Dossier & GLP Liaison

按目标市场格式撰写登记资料,对接 GLP 试验机构。Author dossiers to local formats and liaise with GLP study labs.

🏛️

当地法定代理人Local Legal Agent

以保加利亚实体作为欧盟境内登记持证与法定代理主体,满足属地要求。Our Bulgarian entity acts as the EU-established certificate holder and legal agent.

📊

MRL 与进口容许量MRL & Import Tolerance

最大残留限量查询、申请与进口容许量(Import Tolerance)办理。MRL lookups, applications and import-tolerance filings.

🔄

续展与变更Renewals & Changes

登记证续展、标签变更、扩作与持有人转移等后续事务。Renewals, label changes, uses expansion and holder transfers.

欧盟三大评审分区EU Zonal Assessment

欧盟按分区评审,选对分区是关键The EU Reviews by Zone — Choosing the Right One Matters

依据 (EC) 1107/2009,制剂由选定的牵头成员国(RMS)评审,评审结论只在同一分区内成员国之间互认,跨分区不互认。分区选错,等于把卷宗重做一遍。Under (EC) 1107/2009 a formulation is assessed by a chosen Rapporteur Member State (RMS), and that assessment is recognised only within the same zone — not across zones. Pick the wrong zone and the dossier gets done twice.

保加利亚属 南部分区(Zone C),我们的欧盟总部与持证主体设在此处,南部卷宗路径最短。 需要查某成分在各国已有哪些制剂登记?进入欧盟登记查询 → Bulgaria sits in Zone C (Southern), where our EU headquarters and certificate-holding entity are based — the shortest route for southern dossiers. Looking for existing registrations of a substance by country? Open the EU lookup →
免费查询工具Free Lookup Tool

欧盟农药登记查询EU Pesticide Registration Lookup

覆盖 421 个欧盟已批准活性物质与 24 个成员国的制剂登记记录:支持中文名、英文名、CAS 号模糊搜索,可查批准状态、有效期与法规原文,并提供制剂成分解析、靶标反查与化学类别市场规模。数据随各国官方登记册持续更新。421 EU-approved active substances plus formulation records from 24 member states: fuzzy search by Chinese or English name or CAS number, with approval status, expiry and legal references — plus formulation breakdown, reverse target lookup and market size by chemical class. Updated against national registers.

进入查询 →Open the Tool →
🔎 原药查询Substance Lookup查批准状态、有效期、MRL 与法规链接,支持按状态筛选。Approval status, expiry, MRLs and legal links, filterable by status.
🧪 制剂成分解析Formulation Breakdown输入商品名或成分,自动拆分并核对各原药登记状态。Enter a trade name or composition to break it down and check each active substance.
🎯 靶标反查Reverse Target Lookup按作物与防治对象反查可用有效成分,辅助选药与登记规划。Look up viable active substances by crop and target pest for planning.
工作方式How We Operate

服务流程How We Work

全程透明、分阶段交付,每一阶段都对应明确的预付款与成果。Transparent and phased — every stage maps to a clear prepayment and a defined deliverable.

01

可行性评估Feasibility

明确目标国别、登记类型与数据缺口,出具路线与报价。Define target country, registration type and data gaps; provide roadmap & quote.

02

资料与试验Data & Studies

撰写卷宗、对接 GLP 试验,完成本地化与公证认证。Author dossier, commission GLP studies, localize and notarize.

03

提交与跟进Submission

以当地主体提交,跟踪评审意见并补正答复。Submit via local entity, track queries and respond to deficiencies.

04

获证与维护Certificate

取得登记证,协助续展、变更与市场监管应对。Obtain certificate; assist renewals, changes and post-regulatory needs.

我们的优势Our Edge

为什么选择双润Why Suncoop

我们将是您在目标市场合规延伸的最佳拍档。We will be your best partner for compliance extension in your target markets.

🌍

本地办公室网络Local Presence

在核心市场设办公室,作为登记持证/代理主体。Offices in core markets acting as your local holder/agent.

🗣️

双语专家团队Bilingual Team

中英文资料撰写与官方沟通,消除信息差。ZH/EN authoring and official communication, no lost-in-translation.

📐

分阶段·可控Phased & Controlled

预付一点、交付一点,风险与现金流可控。Pay-as-you-go phases keep risk and cash flow under control.

🔍

透明可追溯Full Transparency

进度、费用、官方来文全程可见可追溯。Progress, fees and official correspondence are fully visible.

📑

登记国本语言交付Native-language Delivery

登记资料、产品标签与 SDS 按成员国官方语言出具,覆盖欧盟 24 种官方语言,不止中英文。Dossiers, labels and SDS in each member state's official language — all 24 official EU languages, beyond ZH/EN.

准备好把产品带进欧盟了吗?Ready to Enter the EU Market?

告诉我们目标成员国与产品类型,获取一份初步可行性评估与报价。Tell us your target member states and product type — get a preliminary feasibility assessment and quote.