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Contents

Long Title

Part I PRELIMINARY

Part II LICENCES AND CERTIFICATES RELATING TO MEDICINAL PRODUCTS

Part III FURTHER PROVISIONS RELATING TO DEALINGS WITH MEDICINAL PRODUCTS

Part IV PHARMACIES

Part V CONTAINERS, PACKAGES AND IDENTIFICATION OF MEDICINAL PRODUCTS

Part VI PROMOTION OF SALES OF MEDICINAL PRODUCTS AND MEDICAL ADVERTISEMENTS

Part VII MISCELLANEOUS AND SUPPLEMENTARY PROVISIONS

FIRST SCHEDULE Diseases and Conditions

SECOND SCHEDULE Amendments to the Poisons Act (Chapter 234)

Legislative History

 
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On 23/05/2013, you requested for the version in force on 23/05/2013 incorporating all amendments published on or before 23/05/2013. The closest version currently available is that of 01/09/2008.
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Special defences under section 20
21.
—(1)  Where the holder of a product licence is charged with an offence under section 20 in respect of any medicinal product which has been manufactured or assembled to his order by another person and has been so manufactured or assembled as not to comply with the provisions of that licence which are applicable to it, it shall be a defence for him to prove —
(a)
that he had communicated those provisions to that other person; and
(b)
that he did not know, and could not by the exercise of reasonable care have discovered, that those provisions had not been complied with.
(2)  Where the holder of a manufacturer’s licence is charged with an offence under section 20 in respect of any medicinal products which have been manufactured or assembled by him, in circumstances where he is not the holder of a product licence which is applicable to those products, but the products were manufactured or assembled to the order of another person, it shall be a defence for him to prove that he believed, and had reasonable grounds for believing —
(a)
that the other person in question was the holder of a product licence applicable to those products; and
(b)
that the products were manufactured or assembled in accordance with that product licence.