Northern Ireland Statutory Rule 2016 United Kingdom

The Animals and Animal Products (Examination for Residues and Maximum Residue Limits) Regulations (Northern Ireland) 2016

At a glance

What's here

4 compliance obligations

Who this Act binds

Business-side actors with duties under this Act, ranked by how often they appear.

  • Any Person 1

Plus 3 non-business duties on Crown ministers, regulators, local authorities or tribunals — shown collapsed under each section below.

Other Acts binding the same actors

For each actor bound by this Act, the other UK Acts that bind them most often. Useful for understanding the full compliance landscape facing each role.

Any Person also bound by 2337 other Acts (top 5 shown)

What this Act requires

Sections that create concrete duties on businesses or carry penalties. Procedural and definitional sections are folded into the “Browse other sections” expander at the bottom of each group. Click any section title to read the source text on legislation.gov.uk.

s.014

Primary analysis of official samples

  • Submit official samples to approved lab for primary analysis Any Person
s.015

Results of primary analysis

Other duties (1) — Crown / regulator
  • Analyst must record test results and notify when residues found Statutory regulator
s.016

Reference analysis

Other duties (1) — Crown / regulator
  • Authorised officer must refer Group A positive samples for reference analysis Crown / Minister / Government department
s.019

Certificates of analysis

Other duties (1) — Crown / regulator
  • Analyst must sign certificates and include officer and enforcement authority details Local authority
Browse 29 other sections — procedural / definitional / commencement
s.001

Citation and commencement

s.002

Interpretation

s.003

Prohibition on the sale of list A and list B substances

s.004

Prohibition on possession of beta-agonists

s.005

Prohibition on administration of beta-agonists or hormonal substances

s.006

Prohibition of administration to animals of unlicensed substances or products

s.007

Prohibition of administration of Table 2 substances

s.008

Prohibition of possession or slaughter of animals and of processing

s.009

Prohibition on the sale of animals

s.010

Prohibition of the sale of animal products

s.011

Prohibition of disposal of a slaughtered animal or batch of animals

s.012

Exception to prohibition on slaughter

s.013

Procurement of samples

s.017

Notification to analyst

s.018

Methods of analysis

s.020

Animal inspections

s.021

Examination of an animal or batch of animals

s.022

Notice on completion of examination

s.023

Offences, penalties and enforcement

s.024

Defences and exceptions

s.025

Compliant Products

s.026

Exception to prohibition on administration for testosterone and progesterone

s.027

Exception to prohibition on administration for allyl trenbolone and beta-agonists

s.028

Exception to prohibition on administration for products having oestrogenic, androgenic or gestagenic action

s.029

Responsibilities of processors

s.030

Unavailability of defence

s.031

Keeping and retention of records

s.032

Application and modification of provisions of the Food Safety (Northern Ireland) Order 1991

s.033

Revocations

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