Control of prohibited drugs and drug residues in the carcass, meat and edible offal of cattle, pigs, sheep, goat, poultry and their products and fish and fishery products intended for human consumption imported into Malaysia.

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Distribution date: 10 August 2004

In order to protect the consumer from dangers of consuming food contaminated with drugs and drug residues, the Ministry of Health Malaysia has been enforcing the ban of the following prohibited drugs in food intended for human consumption since 16 January 1998: Beta-agonists, Nitrofurans and Chloramphenicol. All imported carcass, meat and edible offal of cattle, pigs, sheep, goat, poultry and their products and fish and fishery products intended for human consumption must be accompanied by a Health Certificate from the competent authority stating the absence of the prohibited drugs and drug residues as follows: Beta-agonists in the carcass, meat and edible offal of cattle, pigs, sheep, goat and their products Nitrofurans in the carcass, meat and edible offal of poultry and their products, and fish and fishery products Chloramphenicol in the carcass, meat and edible offal of poultry and their products, and fish and fishery products

Products Covered: The carcass, meat and edible offal of cattle, pigs, sheep, goat, poultry and their products, and fish and fishery products intended for human consumption.

Regulation Type: Regular notification

Human health Food safety Veterinary drugs

Interim Marketing Authorization regarding the use of carrageenan as a stabilizing agent of the water content and sodium carbonate as a pH-adjusting agent in squid meat (available in English and French; pages 2102-2103).

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Distribution date: 06 August 2004

Provision currently exists in the Food and Drug Regulations for the use of carrageenan as a gelling agent and sodium carbonate as a pH-adjusting agent in a variety of foods. Health Canada has received a submission to permit the use of carrageenan as a stabilizing agent of the water content and sodium carbonate as a pH-adjusting agent in squid meat for further processing at levels consistent with good manufacturing practice. Evaluation of available data supports the safety and effectiveness of this new use of carrageenan and sodium carbonate. Therefore, it is the intention of Health Canada to recommend that the Food and Drug Regulations be amended to permit the use of sodium carbonate as a pH-adjusting agent and carrageenan as a stabilizing agent of the water content in squid meat intended for further processing at levels consistent with good manufacturing practice. As a means to improve the responsiveness of the regulatory system, an Interim Marketing Authorization (IMA) is being issued to permit the immediate use of carrageenan and sodium carbonate, as indicated above, while the regulatory process is undertaken to formally amend the Regulations. A revision to this notification will be published at the start of the amendment process and Members will be given the opportunity at that time to submit comments on this proposed measure.

Products Covered: Carrageenan and sodium carbonate (ICS: 67.220.20)

Regulation Type: Regular notification

Food safety Human health Food additives

Interim Marketing Authorization regarding the use of carrageenan as a stabilizing agent of the water content and sodium carbonate as a pH-adjusting agent in squid meat (available in English and French; pages 2102-2103).

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Distribution date: 06 August 2004

Provision currently exists in the Food and Drug Regulations for the use of carrageenan as a gelling agent and sodium carbonate as a pH-adjusting agent in a variety of foods. Health Canada has received a submission to permit the use of carrageenan as a stabilizing agent of the water content and sodium carbonate as a pH-adjusting agent in squid meat for further processing at levels consistent with good manufacturing practice. Evaluation of available data supports the safety and effectiveness of this new use of carrageenan and sodium carbonate. Therefore, it is the intention of Health Canada to recommend that the Food and Drug Regulations be amended to permit the use of sodium carbonate as a pH-adjusting agent and carrageenan as a stabilizing agent of the water content in squid meat intended for further processing at levels consistent with good manufacturing practice. As a means to improve the responsiveness of the regulatory system, an Interim Marketing Authorization (IMA) is being issued to permit the immediate use of carrageenan and sodium carbonate, as indicated above, while the regulatory process is undertaken to formally amend the Regulations. A revision to this notification will be published at the start of the amendment process and Members will be given the opportunity at that time to submit comments on this proposed measure.

Products Covered: Carrageenan and sodium carbonate (ICS: 67.220.20)

Regulation Type: Regular notification

Food safety Human health Food additives

Assessment Reports for Maximum Residue Limits Application A539 (26 pages in English).

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Distribution date: 04 August 2004

This Application seeks to amend the Australia New Zealand Food Standards Code (the Code) to align maximum residue limits (MRLs) for the antibiotic avilamycin in pig commodities so that they are consistent with other national regulations relating to the safe and effective use of agricultural and veterinary chemicals. In administrative terms and consistent with international practice, MRLs assist in regulating the use of agricultural and veterinary chemical products. MRLs indicate whether agricultural and veterinary chemical products have been used in accordance with the registered conditions of use. MRLs in the Code also act to protect public health and public safety by ensuring that chemical residues are no higher than necessary, and act as international trading standards. The MRLs prescribed in the Code constitute a mandatory requirement applying to all food products of a particular class, whether produced domestically or imported. Food products with a residue that exceeds the relevant MRL set out in the Code cannot legally be supplied or sold in Australia. This Application contains variations to MRLs, which are not addressed in the Codex Alimentarius Commission standard. These MRLs may also relate to chemicals used in the production of heavily traded agricultural commodities, which may indirectly affect trade of derivative food products between WTO Members.

Products Covered: Foods in general.

Regulation Type: Regular notification

Food safety Human health Maximum residue limits (MRLs) Veterinary drugs

Assessment Reports for Maximum Residue Limits Application A539 (26 pages in English).

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Distribution date: 04 August 2004

This Application seeks to amend the Australia New Zealand Food Standards Code (the Code) to align maximum residue limits (MRLs) for the antibiotic avilamycin in pig commodities so that they are consistent with other national regulations relating to the safe and effective use of agricultural and veterinary chemicals. In administrative terms and consistent with international practice, MRLs assist in regulating the use of agricultural and veterinary chemical products. MRLs indicate whether agricultural and veterinary chemical products have been used in accordance with the registered conditions of use. MRLs in the Code also act to protect public health and public safety by ensuring that chemical residues are no higher than necessary, and act as international trading standards. The MRLs prescribed in the Code constitute a mandatory requirement applying to all food products of a particular class, whether produced domestically or imported. Food products with a residue that exceeds the relevant MRL set out in the Code cannot legally be supplied or sold in Australia. This Application contains variations to MRLs, which are not addressed in the Codex Alimentarius Commission standard. These MRLs may also relate to chemicals used in the production of heavily traded agricultural commodities, which may indirectly affect trade of derivative food products between WTO Members.

Products Covered: Foods in general.

Regulation Type: Regular notification

Food safety Human health Maximum residue limits (MRLs) Veterinary drugs

TIS 15: Part 12532(1989) Portland Cement: Part 1 Specification (7 pages, available in English)

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Distribution date: 03 August 2004

The Thai Industrial Standards Institute (TISI) has proposed to enforce TIS 15: Part 1-2532(1989) as a mandatory standard. The standard classifies Portland cement into 5 types. Specifies chemical properties (e.g. aluminium oxide, loss on ignition, insoluble residue) and physical properties (e.g. air content of mortar, fineness, time of setting, etc.). Includes packaging, marking and labelling, sampling and criteria for conformity and testing.

Products Covered: Cement, Gypsum, Lime. Mortar (HS Chapter 2523, ICS:  91.100.10)

Regulation Type: Regular notification

TIS 15: Part 12532(1989) Portland Cement: Part 1 Specification (7 pages, available in English)

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Distribution date: 03 August 2004

The Thai Industrial Standards Institute (TISI) has proposed to enforce TIS 15: Part 1-2532(1989) as a mandatory standard. The standard classifies Portland cement into 5 types. Specifies chemical properties (e.g. aluminium oxide, loss on ignition, insoluble residue) and physical properties (e.g. air content of mortar, fineness, time of setting, etc.). Includes packaging, marking and labelling, sampling and criteria for conformity and testing.

Products Covered: Cement, Gypsum, Lime. Mortar (HS Chapter 2523, ICS:  91.100.10)

Regulation Type: Regular notification

Proposed Changes to the Dietary Supplements Regulations 1985. Part two: Sections 4, 5,6 (available in English).

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Distribution date: 26 July 2004

Proposal 1 Amend the Dietary Supplements Regulations 1985 to permit a maximum daily dose of 500mcg of folic acid in a dietary supplement. Proposal 2 Amend the Dietary Supplement Regulations to permit the following sweeteners currently permitted under the Food Standards Code Saccharin or its calcium or ammonium or sodium salt Cyclamate (cyclohexysulphamic acid or its sodium or calcium salt) Aspartame Acesulphame potassium Thaumatin Sucralose Alitame Neotame Proposal 3 Amend the Dietary Supplement Regulations 1985 to include the following labelling provisions currently mandated for food under the Australia New Zealand Food Standards Code: Clause 4 of Standard 1.2.3 [Mandatory Warning and Advisory Statements and Declarations] which provides for the mandatory declaration of substances identified as having potential to cause severe adverse reaction; and Clause 2 of Standard 1.2.9 [Legibility Requirements], which requires food labelling to be written in the English language.

Products Covered: Proposal 1 Folic Acid Supplements Proposal 2 Artificial Sweeteners Proposal 3 Cereals containing gluten and their products, wheat, rye, barley, oats and spelt Crustacea and their products Eggs and egg products Fish and fish products Milk and mild products 789 Peanuts and soybeans, and their products Added sulphites in concentrations of 10 mg/kg or more Tree nuts and sesame seeds and their products.

Regulation Type: Regular notification

Food safety Labelling Human health

Proposed Changes to the Dietary Supplements Regulations 1985. Part two: Sections 4, 5,6 (available in English).

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Distribution date: 26 July 2004

Proposal 1 Amend the Dietary Supplements Regulations 1985 to permit a maximum daily dose of 500mcg of folic acid in a dietary supplement. Proposal 2 Amend the Dietary Supplement Regulations to permit the following sweeteners currently permitted under the Food Standards Code Saccharin or its calcium or ammonium or sodium salt Cyclamate (cyclohexysulphamic acid or its sodium or calcium salt) Aspartame Acesulphame potassium Thaumatin Sucralose Alitame Neotame Proposal 3 Amend the Dietary Supplement Regulations 1985 to include the following labelling provisions currently mandated for food under the Australia New Zealand Food Standards Code: Clause 4 of Standard 1.2.3 [Mandatory Warning and Advisory Statements and Declarations] which provides for the mandatory declaration of substances identified as having potential to cause severe adverse reaction; and Clause 2 of Standard 1.2.9 [Legibility Requirements], which requires food labelling to be written in the English language.

Products Covered: Proposal 1 Folic Acid Supplements Proposal 2 Artificial Sweeteners Proposal 3 Cereals containing gluten and their products, wheat, rye, barley, oats and spelt Crustacea and their products Eggs and egg products Fish and fish products Milk and mild products 789 Peanuts and soybeans, and their products Added sulphites in concentrations of 10 mg/kg or more Tree nuts and sesame seeds and their products.

Regulation Type: Regular notification

Food safety Labelling Human health

Interim Marketing Authorization regarding the use of microcrystalline cellulose as a bodying and texturizing agent in breath freshening strips (available in English and French; pages 1953-1954).

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Distribution date: 26 July 2004

Provision currently exists in the Food and Drug Regulations for the use of microcrystalline cellulose as a bodying and texturizing agent in a variety of foods. Health Canada has received a submission to permit the use of microcrystalline cellulose as a bodying and texturizing agent in breath freshening strips at a maximum level of use of nine percent. Evaluation of available data supports the effectiveness and safety of this new use for microcrystalline cellulose. Therefore, it is the intention of Health Canada to recommend that the Food and Drug Regulations be amended to permit the optional use of microcrystalline cellulose as a bodying and texturizing agent in the manufacture of breath freshening strips at a maximum level of use of nine percent. As a means to improve the responsiveness of the regulatory system, an Interim Marketing Authorization (IMA) is being issued to permit the immediate use of microcrystalline cellulose, as indicated above, while the regulatory process is undertaken to formally amend the Regulations. A revision to this notification will be published at the start of the amendment process and Members will be given the opportunity at that time to submit comments on this proposed measure

Products Covered: Microcrystalline cellulose (ICS: 67.180.20)

Regulation Type: Regular notification

Food safety Food additives Human health

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