Statutory Instrument 1993 No. 3050

      The Notification of New Substances Regulations 1993


      © Crown Copyright 1993

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STATUTORY INSTRUMENTS

1993 No. 3050

HEALTH AND SAFETY

The Notification of New Substances Regulations 1993

Made 15th December 1993
Laid before Parliament 23rd December 1993
Coming into force 31st January 1994


ARRANGEMENT OF REGULATIONS

PART I
Interpretation and General
1.  Citation and commencement
2.  Interpretation
3.  Application
PART II
Notifications
4.  Full notifications
5.  Requirements for further testing for substances notified under regulation 4
6.  Reduced notification requirements for substances placed on the market in quantities of less than one tonne per year by a single manufacturer
7.  Notifications relating to polymers
8.  Placing of notified substances on the market
9.  Requirements for further information
10.  Follow-up information
11.  Notification of substances previously notified
12.  Substances manufactured outside the Communities
13.  Further notifications of the same substances and avoidance of duplication of testing on vertebrate animals
14.  Tests under these Regulations to conform to the principles of good laboratory practice
15.  Notifications and reports to be in English
PART III
Rights and Duties of the Competent Authority
16.  Risk assessments
17.  Information to be sent by the competent authority to the European Copmmission
PART IV
Disclosure of Information
18.  Disclosure of information provided under Part II of these Regulations
19.  Treatment of confidential information
20.  Substances appearing in the list of notified substances
PART V
Miscellaneous and General
21.  Enforcement and civil liability
22.  Prohibition of importation and placing on the market of unnotified substances
23.  Exemption certificates
24.  Fees for notifications etc.
25.  Revocations, amendments and transitional provisions

  Schedule 1  Characteristic properties of dangerous substances

  Schedule 2  Information required to be in the technical dossiers (which sets out the provisions of Annex VII to the Directive)

  Schedule 3  Additional information and tests required under regulation 5 (which set out the provisions of Annex VIII to the Directive)

  Schedule 4  Fees for notifications etc.

 

Explanatory Note


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Prepared 20th September 2000