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The Adequacy of the Mauritian Biosafety Framework

Published online by Cambridge University Press:  02 January 2014

Abstract

This article analyses the Mauritian regulatory framework on genetically modified organisms (GMOs) and highlights its shortcomings, with the aim of improving the regulation of the approval and monitoring of the use of GMOs in Mauritius. It examines key issues regarding the application for a GMO permit, risk assessment requirements, identification and labelling obligations, post-market monitoring, and liability and redress in the case of damages. There is a need for greater public participation in decision-making on the approval of GMO permits and the monitoring stage procedure, specific civil liability provisions for damage as well as regulation of the coexistence of genetically modified (GM) and non-GM crops in the Mauritian biosafety framework. Pending the proclamation of the entire Mauritian GMO Act 2004, relevant transitional provisions should also be provided. Beyond legal provisions on biosafety, a national policy on GM products and GMO-related activities should be elaborated.

Type
Research Article
Copyright
Copyright © SOAS, University of London 2014 

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References

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8 Any living organism that possesses a novel combination of genetic material obtained through the use of modern biotechnology and is capable of replication as per art 3(g) of the Cartagena Protocol. An LMO is a sub-category of the broader category of GMOs. The Cartagena Protocol refers to LMOs rather than GMOs because there was controversy on the scope of GMOs to be covered during the negotiation of this protocol. It was finally agreed that the protocol will cover only transboundary movements of LMOs to the extent that they may have a potential impact on biological diversity while not all GMOs as a broader category may have any impact on biological diversity. Both terms are used in this paper.

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25 Act 3 of 2004.

26 Cartagena Protocol, art 1.

27 GMO Act, sec 6(2)(b).

28 Act 10 of 2006.

29 Act 1 of 1998.

30 GMO Act, sec 2.

31 An organism means a cellular or non-cellular biological entity, capable of metabolism, replication, reproduction or of transferring genetic material and includes a microorganism. Art 3(h) of the Cartagena Protocol defines a “living organism” as “any biological entity capable of transferring or replicating genetic material, including sterile organisms, viruses and viroids”.

32 Art 1 of the draft African Model Law on Biosafety includes the “products of a GMO” which it defines as “any material derived by processing, or otherwise, from any genetically modified organism or from a product of a genetically modified organism”.

33 GMO Act, sec 3(1)(a).

34 Id, sec 3(1)(b).

35 Id, sec 3(1)(c).

36 Id, sec 3(2).

37 Id, sec 2.

38 Ibid.

39 A “facility” means any place where activities involving GMOs are carried on (for instance a building, laboratory, greenhouse, insectary or field).

40 See the first sched of the GMO Act. Category A enumerates the different kinds of trials targeted: laboratory experimentation, greenhouse trial, small field testing and large field trial.

41 Ibid. See the request for approval of a GMO permit: category B food and feedstuffs.

42 Neeliah et al National Policy Regarding Commercial GM Imports, above at note 19 at 5.

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46 All designated national focal points are registered in the biosafety clearing house in accordance with art 19 of the Cartagena Protocol.

47 The International Centre for Genetic Engineering and Biotechnology in collaboration with the Faculty of Agriculture of the University of Mauritius and the FARC held a three day stakeholder workshop on biosafety risk communication in June 2011. FARC, which operates under the Ministry of Agro Industry and Food Security, held (with the support of UNEP and GEF) a one day workshop on public information and participation regarding biosafety issues in March 2011. A two day workshop on handling applications for GMO permits was held in March 2009. Details are on file with the author.

48 GMO Act, sec 4(1).

49 The minister may revoke appointments in accordance with powers given to him under sect 4(2)(b) of the GMO Act, for any reason specified in sec 37(3)(b) of the Interpretation and General Clauses Act 33 of 1974.

50 See the second national report for Mauritius submitted in September 2011, available at: <http://bch.cbd.int/database/record.shtml?documentid=102328> (last accessed 7 May 2012).

51 GMO Act, sec 2.

52 Id, sec 19(2).

53 Id, sec 7.

54 Id, sec 7(3)(a).

55 There should be advance informed consent before the export of GM products in accordance with art 7 of the Cartagena Protocol and art 1 of the draft African Model Law on Biosafety.

56 Cartagena Protocol, art 11.

57 Art 13(1) and 13(2) of the draft African Model Law on Biosafety mention the need for a threshold below 0.9% for adventitious presence of GMOs.

58 GMO Act, sec 16(2).

59 Neeliah et al National Policy Regarding Commercial GM Imports, above at note 19 at 16.

60 Plant Protection Act 2006, sec 18.

61 Id, secs 22 and 23.

62 Id, sec 24.

63 Cartagena Protocol, art 23.

64 GMO Act, second sched.

65 Art 10(6) of the Cartagena Protocol acknowledges that there are scientific uncertainties due to lack of information and relevant scientific knowledge on the extent of negative effects of an LMO on conservation and sustainable biodiversity.

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69 Environment Protection Act 19 of 2002, sec 5.

70 The following are also included: impacts likely to occur as a result of substituting traditional crops, products and indigenous technologies through modern biotechnology out of their agro-climatic zones; anticipated social and economic costs due to loss of genetic diversity, market opportunities and, in general, means of livelihood of the communities likely to be affected by the introduction of the GMOs or products and; possible effects which are contrary to the social, cultural, ethical and religious values of communities arising from the use or release of the GMO.

71 GMO Act, sec 18.

72 Id, sec 20.

73 Id, sec 20(2)(a) and (b).

74 Id, sec 20(1).

75 Strategic Options in Crop Diversification and Livestock Sector (2007–15) (consultation draft, 2007, Ministry of Agro Industry and Fisheries) at 60.

76 Id at 58.

77 GMO Act, sec 21(1).

78 Food Regulations 1999, made by the minister under sec 18 of the Food Act 1998.

79 See id, sec 2: “pre-packed food” means “food, including cooked and uncooked which has been packed in a container before being sold to [sic] ultimate consumer, and which is sealed in such a manner that the contents cannot in any way be altered without the package being opened or undergoing perceptible modifications”.

80 Id, sec 3(1)(m).

81 See draft African Model Law on Biosafety, annex II C; Van Tassel, KAGenetically modified plants used for food, risk assessment and uncertainty principles: Does the transition from ignorance to indeterminacy trigger the need for post-market surveillance” (2009) 15 Boston University Journal of Science & Technology LawGoogle Scholar 220 at 222.

82 Codex Alimentarius “General Standard for the Labelling of Prepacked Foods (1985)”: CODEX STAN 1-1985, available at <http://www.codexalimentarius.org/standards/list-of-standards/> (last accessed 30 November 2013).

83 Art 18(1) of the Cartagena Protocol refers to international rules and standards.

84 Draft African Model Law on Biosafety, art 13(2).

85 Neeliah et al National Policy Regarding Commercial GM Imports, above at note 19 at 16.

86 Previously the labelling of GM foods was based on regulation (EC) 258/97 on novel foods and novel food ingredients (Official Journal L43, 14 February 1997 at 1–6) but regulation (EC) 1829/2003 on genetically modified food and feed (Official Journal L268, 18 October 2003 at 1) provides a more comprehensive regime on the labelling of GM food and feed products.

87 Compton “Applying World Trade Organization rules”, above at note 68 at 385.

88 See the Swiss Federal Law relating to Non-Human Gene Technology (2003) Recueil systématique 814.91.

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90 Reg 7 (GN no R 293 of 1 April 2011) in terms of sec 120(1) of the Consumer Protection Act 68 of 2008.

91 Act 32 of 1977.

92 GMO Act, sec 11.

93 Id, sec 10.

94 Id, sec 23(1).

95 Mauritian Civil Code, arts 1382 and 1383.

96 The Nagoya-Kuala Lumpur Supplementary Protocol on Liability and Redress to the Cartagena Protocol on Biosafety, adopted in October 2012, available at: <http://bch.cbd.int/protocol/supplementary/> (last accessed 2 May 2012).

97 See GMO Act, sec 24(1): the minister may make any regulation he thinks fit for the purposes of the act.

98 Only secs 1–5, 6(1)(a)–(c) and 24 have been proclaimed; they entered into force on 1 January 2005.