欧洲(非欧盟)Europe (non-EU)
🇬🇧

英国United Kingdom

脱欧后独立登记体系,与欧盟平行Independent post-Brexit regime running parallel to the EU

主要作物Key Crops
小麦 / 油菜 / 马铃薯 / 牧草Wheat / Rapeseed / Potato / Grass
农业占 GDPAgri GDP Share
约 1%~1%
核心产区Core Region
英格兰 / 苏格兰England / Scotland
监管体系Regime
GB 独立体系Independent GB Regime

01农业基本情况Agricultural Overview

市场规模、主要作物与农业结构Market scale, key crops and farm structure

英国农业以谷物、油菜、马铃薯与畜牧业为主,英格兰低地、苏格兰与威尔士草场各具特色。脱欧后,农药管理建立独立的 GB(大不列颠)体系,与北爱尔兰安排不同,需分别对待。UK agriculture centers on cereals, rapeseed, potatoes and livestock; England's lowlands and Scottish/Welsh pastures differ. Post-Brexit, pesticide regulation runs as an independent GB (Great Britain) regime, distinct from Northern Ireland — treat them separately.

  • GB 与 EU 体系平行但独立。GB and EU regimes run parallel but separate.
  • 北爱尔兰适用不同安排。Northern Ireland follows a different arrangement.
  • 残留限量参考但需独立核对。MRLs are referenced but checked independently.

02农药基本情况Pesticide Overview

主管机构、登记制度与市场Authority, registration system and market

主管机构Regulatory Authority

GB 农药登记由健康与安全执行局(HSE)下属的化学法规司(CRD)负责。GB pesticide registration is handled by HSE's Chemicals Regulation Division (CRD).

登记制度Registration System

脱欧后英国建立独立的 GB 登记体系;可参考欧盟数据但需单独提交与评审,标签须英文(及威尔士语如适用)。The UK built an independent GB regime; EU data can inform but must be submitted and reviewed separately; labels in English (and Welsh where applicable).

市场概况Market Snapshot

成熟、规范的高端市场。A mature, regulated premium market.

  • 须有英国境内主体或授权代理。A UK-established entity or authorized agent is required.
  • 原药需 GB 层面的评估/认可。AI needs GB-level assessment / recognition.
  • 资料以英文提交。Documents in English.

03登记注册门槛Registration Thresholds

取得英国登记的一般门槛(初稿,供参考):General thresholds for a UK registration (draft, for reference):

1申请人资格Eligibility

英国境内设立的主体或授权代理人。A UK-established entity or authorized agent.

2技术资料Technical Dossier

毒理、生态、残留与药效数据。Toxicology, ecotox, residue and efficacy data.

3原药评估AI Assessment

原药须取得 GB 层面认可。AI must gain GB-level recognition.

4标签合规Label Compliance

英文标签符合 GB 格式要求。English labels per GB format rules.

04登记周期与时间Registration Timeline

典型登记周期(仅供参考):Typical timeline (indicative):

资料准备Data Prep

3–9 个月3–9 months

撰写、翻译与本地化。Author, translate and localize.

CRD 评审CRD Review

12–24+ 个月12–24+ months

技术评审与补正。Technical review and deficiencies.

核发Issuance

1–3 个月1–3 months

获证与公示。Certificate and publication.

提示Note:整体约 1.5–2.5 年,视资料完整度。Overall ~1.5–2.5 years depending on dossier completeness.

05联系我们Contact Us

该国本地办公室与对接人Local office and point of contact for this market

🏢
办公室Office · 伦敦办公室 · 英国及爱尔兰业务部London Office · UK & Ireland Desk
英国诺福克郡诺里奇 诺里奇研究园 NR4 7TJNorwich Research Park, Norwich, Norfolk, NR4 7TJ, United Kingdom
📞
电话Phone
+44 20 7000 0000
✉️
邮箱Email
alan@suncoop.cn
🕘
工作时间Hours
周一至周五 9:00–18:00 (GMT+2)Mon–Fri 9:00–18:00 (GMT+2)
📍
英国诺福克郡诺里奇 诺里奇研究园 NR4 7TJNorwich Research Park, Norwich, Norfolk, NR4 7TJ, United Kingdom
免责声明Disclaimer: 本页登记主管机构、流程与周期为基于公开资料的初稿,标注"以官方为准"。具体登记要求、周期与费用以各国官方主管部门最新规定为准,正式提交前请由专业顾问核实。本网站不构成法律或合规意见。The authorities, procedures and timelines on this page are a draft based on public sources, marked "subject to official rules". Exact requirements, timelines and fees are governed by each national authority's latest regulations and must be verified by a professional advisor before filing. This site is not legal or compliance advice.