BỘ Y TẾ |
CỘNG HÒA XÃ HỘI CHỦ NGHĨA VIỆT NAM |
Số: 20/2012/TT-BYT |
Hà Nội, ngày 15 tháng 11 năm 2012 |
BAN HÀNH QUY CHUẨN KỸ THUẬT QUỐC GIA ĐỐI VỚI SẢN PHẨM DINH DƯỠNG CÔNG THỨC CHO TRẺ ĐẾN 12 THÁNG TUỔI
BỘ TRƯỞNG BỘ Y TẾ
Căn cứ Luật an toàn thực phẩm ngày 17 tháng 6 năm 2010 và Nghị định số 38/2012/NĐ-CP ngày 25 tháng 4 năm 2012 của Chính phủ Quy định chi tiết thi hành một số điều của Luật an toàn thực phẩm;
Căn cứ Luật tiêu chuẩn và quy chuẩn kỹ thuật ngày 29 tháng 6 năm 2006 và Nghị định số 127/2007/NĐ-CP ngày 01 tháng 8 năm 2007 của Chính phủ Quy định chi tiết thi hành một số điều của Luật tiêu chuẩn và quy chuẩn kỹ thuật;
Căn cứ Nghị định số 63/2012/NĐ-CP ngày 31 tháng 8 năm 2012 của Chính phủ Quy định chức năng, nhiệm vụ, quyền hạn và cơ cấu tổ chức của Bộ Y tế;
Theo đề nghị của Cục trưởng Cục An toàn thực phẩm;
Bộ trưởng Bộ Y tế ban hành Thông tư ban hành quy chuẩn kỹ thuật quốc gia đối với sản phẩm dinh dưỡng công thức cho trẻ đến 12 tháng tuổi.
Điều 1. Ban hành kèm theo Thông tư này:
QCVN 11-1:2012/BYT - Quy chuẩn kỹ thuật quốc gia đối với sản phẩm dinh dưỡng công thức cho trẻ đến 12 tháng tuổi;
Điều 2. Thông tư này có hiệu lực kể từ ngày 01 tháng 6 năm 2013.
Điều 3. Cục trưởng Cục An toàn thực phẩm, thủ trưởng các đơn vị thuộc Bộ Y tế, các đơn vị trực thuộc Bộ Y tế; giám đốc Sở Y tế các tỉnh, thành phố trực thuộc trung ương và các tổ chức, cá nhân có liên quan chịu trách nhiệm thi hành Thông tư này./.
Nơi nhận: |
KT. BỘ TRƯỞNG |
THE MINISTRY
OF HEALTH |
SOCIALIST
REPUBLIC OF VIETNAM |
No. 20/2012/TT-BYT |
Hanoi, November 15th 2012 |
THE MINISTER OF HEALTH
Pursuant to the Law of Food safety dated June 17th 2010 and the Government's Decree No. 38/2012/ND-CP dated April 25th 2012, detailing the implementation of a number of articles of the Law of Food safety;
Pursuant to the Law on Technical regulations and standards dated June 29th 2006 and the Government's Decree No. 127/2007/ND-CP dated August 01st 2007 detailing the implementation of a number of articles of the Law on Technical regulations and standards;
Pursuant to the Government's Decree No. 63/2012/ND-CP dated August 31st 2012 defining the functions, tasks, powers and organizational structure of the Ministry of Health;
At the request of the Director of Vietnam Food Administration;
The Minister of Health issues a Circular promulgating the National Technical Regulation on infant formula( for children up to 12 months of age).
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Article 2. This Circular takes effect on June 01st 2013.
Article 3. The Director of Vietnam Food Administration, heads of units affiliated to the Ministry of Health, the Directors of Services of Health, relevant organizations and individuals are responsible for the implementation of this Circular./.
PP THE
MINISTER
DEPUTY MINISTER
Nguyen Thanh Long
PROMULGATING THE NATIONAL TECHNICAL REGULATION
ON INFANT FORMULA( FOR CHILDREN UP TO 12 MONTHS OF AGE)
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QCVN 11-1:2012/BYT is submitted by Vietnam Food Administration and promulgated together with the Circular No. 20/2012/TT-BYT dated November 15th 2012 of the Minister of Health.
PROMULGATING THE NATIONAL TECHNICAL REGULATION
ON FORMULATED FOODS FOR CHILDREN UP TO 12 MONTHS
1. Scope of regulation
This Regulation deals with the food safety standards of food safety and quality, and the requirements of the management of infant formula for children up to 12 months of age (hereinafter referred to as infant formula).
2. Subjects of application
This Regulation is applicable to:
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2.2. Relevant State management agencies
3. Interpretation of terms and abbreviations
In this Regulation, the terms and abbreviations below are construed as follows:
3.1. Infant formula are liquid or powdered products that satisfy the nutritional requirements of children up to 12 months of age (hereinafter referred to as infants), that are made from:
- Cow’s milk or other animals’ milk or their mixture,
- Other appropriate ingredients.
Infant formula could be used as a breast-milk substitute as prescribed in the Joint Circular No. 10/2006/TTLT/BYT-BTM-BVHTT-UBDSGDTE dated August 25th 2006, guiding the implementation of the Government's Decree No. 21/2006/ND-CP dated February 27th 2006 on the trade and use of dietary products for children.
3.2. GUL: Guidance Upper Level. These levels are for nutrients without sufficient information for a science-based risk assessment. These values are established based on the fulfillment of nutritional requirements of infants and the information about safe use. They may be adjusted based on relevant scientific or technological progress. The purpose of the GULs is to provide guidance for producers and they should not be interpreted as goal values.
Nutrient contents in infant formulas must not exceed the GULs unless higher nutrient levels cannot be avoided due to the change in ingredients or due to technological reasons. Producers must not increase the levels of nutrients to reach GULs when that of their products are lower than GUL.
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3.4. DHA: Docosahexaenoic acid.
3.5. IU: International Unit.
3.6. PUFA: Poly-unsaturated Fatty Acids.
1. Fundamental constituents
1.1. General requirements
1.1.1. Ingredients and food additives in the production must ensure the food safety and hygiene, be gluten-free, and suitable for the digestion of infants.
1.1.2. Nutritional safety and the nutritional adequacy must be scientifically proved to support the growth and development of infants.
1.2. Energy
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Unit
Minimum
Maximum
kcal/100 ml
60
70
kJ/100 ml
250
295
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Infant formula (prepared ready for consumption as recommended by the producer) must satisfy the following criteria:
1.3.1. Protein 1), 2), 3)
Unit
Minimum 4)
Maximum
GUL
Notes
g/100 kcal
1.8
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–
Applicable to products from cow’s milk protein.
2.25
3.0
–
Applicable to products from soy protein.
g/100 kJ
0.45
0.7
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Applicable to products from cow’s milk protein.
0.5
0.7
–
Applicable to products from soy protein.
Notes:
1) Protein content in infant formula (prepared ready for consumption as recommended by the producer) is equal to N x 6.25 (N is nitrogen content). Scientific justification must be provided for the use of a different conversion factor. The protein levels in this Regulation are based on the nitrogen conversion factor of 6.25. The value of 6.38 is generally established as a specific factor appropriate for conversion of nitrogen to protein in other milk products, and the value of 5.71 as a specific factor for conversion of nitrogen to protein in other soy products.
2) For an equal energy value, the product must contain an available quantity of each essential and semi-essential amino acid at least equal to that contained in the breast-milk (the reference values are provided in Annex I of this Regulation); for calculation purposes, the concentrations of tyrosine and phenylalanine may be added together. The concentrations of methionine and cysteine may be added together if the ratio is less than 2:1; in case the ratio is between 2:1 and 3:1, the suitability of the product has to be proved by clinical testing.
3) Isolated amino acids may be added to infant formula only to improve its nutritional value. Essential and semi-essential amino acids may be added only in amounts necessary for improving protein quality. Only L-forms of amino acids shall be used.
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1.3.2. Lipids
Unit
Minimum
Maximum
GUL
Notes
Total fat 5), 6)
5) Hydrogenated oils and fats shall not be used in infant formula.
6) Lauric and myristic acids are constituents of fats, but their total amount must not exceed 20% of total fatty acids. The amount of trans fatty acids must not exceed 3 % of total fatty acids. Trans fatty acids are endogenous components of milk fat Up to 3% of trans fatty acids is accepted for the use of milk fat in infant formula. The amount of erucic acid must not exceed 1% of total fatty acids. The amount of phospholipids should not exceed 300 mg/100 kcal (72 mg/100 kJ).
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4.4
6.0
–
g/100 kJ
1.05
1.4
–
Linoleic acid
mg/100 kcal
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–
1,400
mg/100 kJ
70
–
330
a-linolenic acid
mg/100 kcal
50
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–
mg/100 kJ
12
–
–
Ratio of linoleicacid to a-linolenic acid
5:1
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1.3.3. Carbohydrates
Unit
Minimum
Maximum
GUL
Notes
Total carbohydrates 7)
7) Lactose and glucose polymers should be the preferred carbohydrates in products derived from cows’ milk protein and hydrolyzed protein. Only precooked and/or gelatinized starches gluten-free by nature may be added to products with an amount up to 30% of total carbohydrates and up to 2 g/100 ml. Because of potential threats to young infants with hereditary fructose intolerance, the use of sucrose and fructose in products should be avoided unless needed.
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9.0
14.0
–
g/100 kJ
2.2
3.3
–
1.3.4. Vitamins
Unit
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Maximum
GUL
Notes
Vitamin A
8) Expressed as µg RE. 1 µg RE = 3.33 IU Vitamin A = 1 µg all-trans retinol. Retinol contents shall be provided by preformed retinol, not including the amount of carotenoids in vitamin A.
mg8)/100 kcal
60
180
–
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14
43
–
Vitamin D3
9) Expressed as calciferol.
1 mg calciferol = 40 IU vitamin D
mg9) /100kcal
1
2.5
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mg9) /100 kJ
0.25
0.6
–
Vitamin E
10) Expressed as a-tocopherol equivalent (a-TE).
1 mg a-TE = 1 mg d-a-tocopherol
11) Vitamin E content shall be at least 0.5 mg α-TE per g PUFA, using the following factors of equivalence to adapt the minimal vitamin E content to the number of fatty acid double bonds in the product: 0.5 mg -TE/g linoleic acid (18:2 n-6); 0.75 α-TE/g α-linolenic acid (18:3 n-3); 1.0 mg α-TE/g arachidonic acid (20:4 n-6); 1.25 mg α-TE/g eicosapentaenoic acid (20:5 n-3); 1.5 mg α-TE/g docosahexaenoic acid (22:6 n-3)
mg10)/100 kcal
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–
5
mg10)/100 kJ
0.1211)
–
1.2
Vitamin K
mg/100 kcal
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–
27
mg/100 kJ
1
–
6.5
Vitamin B1 (Thiamin)
mg/100 kcal
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Mọi chi tiết xin liên hệ: ĐT: (028) 3930 3279 DĐ: 0906 22 99 66
–
300
mg/100 kJ
14
–
72
Vitamin B2 (Riboflavin)
mg/100 kcal
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Mọi chi tiết xin liên hệ: ĐT: (028) 3930 3279 DĐ: 0906 22 99 66
–
500
mg/100 kJ
19
–
119
Niacin12)
12) Applicable to preformed niacin
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300
–
1,500
mg/100 kJ
70
–
360
Vitamin B6
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35
–
175
mg/100 kJ
8.5
–
45
Vitamin B12
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0.1
–
1.5
mg/100 kJ
0.025
–
0.36
Pantothenic acid
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400
–
2,000
mg/100 kJ
96
–
478
Folic acid
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10
–
50
mg/100 kJ
2.5
–
12
Vitamin C
13) Expressed as ascorbic acid
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mg13)/100kcal
10
–
70 14)
mg13)/100 kJ
2.5
–
17 14)
Vitamin H (Biotin)
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mg/100 kcal
1.5
–
10
mg/100 kJ
0.4
–
2.4
The vitamins added in products must comply with the regulations of the Ministry of Health. The cases not provided for by the Ministry of Health must comply with the instructions of CODEX in CAC/GL 10-1979, Rev.1-2008 Advisory List of Mineral Salts and Vitamin compounds for Use in Foods for Infants and Children.
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Unit
Minimum
Maximum
GUL
Notes
Iron
mg/100 kcal
0.45
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Mọi chi tiết xin liên hệ: ĐT: (028) 3930 3279 DĐ: 0906 22 99 66
–
mg/100 kJ
0.1
–
–
Calcium
mg/100 kcal
50
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Mọi chi tiết xin liên hệ: ĐT: (028) 3930 3279 DĐ: 0906 22 99 66
140
mg/100 kJ
12
–
35
Phosphorus
15) This GUL should accommodate higher needs with soy formula.
mg/100 kcal
25
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100(15)
mg/100 kJ
6
–
24(15)
Ratio of calcium to phosphorus
1 :1
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–
Magnesium
mg/100 kcal
5
–
15
mg/100 kJ
1.2
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3.6
Sodium
mg/100 kcal
20
60
–
mg/100 kJ
5
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Mọi chi tiết xin liên hệ: ĐT: (028) 3930 3279 DĐ: 0906 22 99 66
–
Chloride
mg/100 kcal
50
160
–
mg/100 kJ
12
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Mọi chi tiết xin liên hệ: ĐT: (028) 3930 3279 DĐ: 0906 22 99 66
–
Potassium
mg/100 kcal
60
180
–
mg/100 kJ
14
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–
Manganese
mg/100 kcal
1
–
100
mg/100 kJ
0.25
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24
Iodine
mg/100 kcal
10
–
60
mg/100 kJ
2.5
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14
Selenium
mg/100 kcal
1
–
9
mg/100 kJ
0.24
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2.2
Copper
mg/100 kcal
35
–
120
mg/100 kJ
8.5
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Mọi chi tiết xin liên hệ: ĐT: (028) 3930 3279 DĐ: 0906 22 99 66
29
Zinc
mg/100 kcal
0.5
–
1.5
mg/100 kJ
0.12
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Mọi chi tiết xin liên hệ: ĐT: (028) 3930 3279 DĐ: 0906 22 99 66
0.36
The minerals and trace elements added in products must comply with the regulations issued by the Ministry of Health. The cases not provided for by the Ministry of Health must comply with the instructions of CODEX in CAC/GL 10-1979, Rev.1-2008 Advisory List of Mineral Salts and Vitamin compounds for Use in Foods for Infants and Children.
1.3.6. Other ingredients
Unit
Minimum
Maximum
GUL
Notes
Choline
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mg/100 kcal
7
–
50
mg/100 kJ
1.7
–
12
Myo-inositol
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mg/100 kcal
4
–
40
mg/100 kJ
1
–
9.5
L-Carnitine
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mg/100 kcal
1.2
–
–
mg/100 kJ
0.3
–
–
2. Optional ingredients
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Scientific justification for the safety and suitability for nutritional uses of infants must be provided. The amount of these ingredients in infant formula must be sufficient to achieve the intended effect (with account taken of their amount in breast-milk).
Criteria for optional ingredients:
Unit
Minimum
Maximum
GUL
Notes
Taurine
In infant formula prepared ready for consumption as recommended by the producer
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–
12
–
mg/100 kJ
–
3
–
Docosahexaenoic acid 16)
In infant formula prepared ready for consumption as recommended by the producer
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% of fatty acids
–
–
0.5
- Only cultures that produce L(+)lactic acid may be used.
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- Fluoride should not be added to infant formula.
- Fluoride content:
Unit
Maximum
Notes
mg/100 kcal
100
In infant formula prepared ready for consumption as recommended by the producer
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24
4. Requirements after preparation
After being prepared ready for consumption as recommended by the producer, the products must be suitable for infants and free of lumps
5. Processing by ionizing irradiation
The product and ingredients must not be treated by ionizing irradiation
6. Food additives
The food additives used in infant formula must comply with the provisions of the Ministry of Health.
7. Contaminants
7.1. Pesticide residues
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If pesticide residues are technically unavoidable, they must be reduced to the maximum extent possible.
8.2. Melamine
Unit
Maximum
Notes
mg/kg
1
In powdered infant formula
8.3. Heavy metal
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8.4. Mycotoxin
Specified in QCVN 8-1:2011/BYT – National Technical Regulation on the limit of mycotoxin contamination in food
8.5. Other contaminants
The product must not contain undesirable substances (e.g. biologically active substances) in amounts which may harm the health of infants.
The products covered by the provisions of this Regulation shall comply with the maximum limits prescribed by the Ministry of Health. Codex’s provisions shall apply if the Ministry of Health does not have specific provisions.
9. Microorganisms
Specified in QCVN 8-3:2012/BYT – National Technical Regulation on the limit of mycotoxin contamination in food.
10. Labeling
The labels of infant formula must comply with the Government's Decree No. 89/2006/ND-CP dated August 30th 2006 on goods labels, the Government's Decree No. 21/2006/ND-CP dated February 27th 2006 on the trade and use of dietary products for young infants, and their guiding documents.
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1. Sampling
The sampling method is specified in the Circular No. 16/2009/TT-BKHCN dated June 02nd 2009 of the Ministry of Science and Technology on the inspection of goods quality; the Circular No. 14/2011/TT-BYT dated April 01st 2011 of the Ministry of Health, guiding the sampling of foods serving the inspection of food quality, safety and hygiene, and relevant laws.
2. Test methods
The technical requirements in this Regulation must be tested using the methods in Annex 2 of this Regulation (these methods are not compulsory, and equivalent test methods may be used)
When inspecting the standards using the test methods that are not stated in this Regulation, the Ministry of Health shall provide the accredited methods in Vietnam or abroad.
IV. PROVISIONS FOR THE MANAGEMENT
1. Declaration of conformity
1.1. Infant formula must have the declaration of conformity before being imported, produced, or sold in Vietnam in accordance with this Regulation.
1.2. The formality and procedure for declaration of conformity are provided in the Government's Decree No. 38/2012/ND-CP dated April 25th 2012, detailing the implementation of a number of articles of the Law of Food safety, the Circular No. 19/2012/TT-BYT dated September 11th 2012, guiding the declaration of conformity and declaration of compliance to food safety regulations, and other laws.
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The safety and quality inspection of infant formula must comply with law.
V. RESPONSIBILITY OF ORGANIZATIONS AND INDIVIDUALS
1. Infant formula producers, importers, and traders must make the declaration of conformity in accordance with the technical provision in this Regulation, and register the declaration of conformity at a competent agency under the appointment of the Ministry of Health, and ensure the declared quality and safety.
2. Infant formula is only produced, imported, or sold after the declaration of conformity is registered, and the quality, safety, labels are conformable with law.
VI. IMPLEMENTATION ORGANIZATION
1. Vietnam Food Administration shall cooperate with relevant functional agencies in the implementation of this Regulation.
2. Vietnam Food Administration shall request the Ministry of Health to amend this Regulation based on the requirements of management.
3. Where the standards and law cited in this Regulation are amended or replaced, the newer ones shall apply.
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REFERENCE AMOUNTS OF ESSENTIAL AND SEMI-ESSENTIAL AMINO ACIDS IN BREAST-MILK
No.
Amino acid
Average amount
mg/g nitrogen
mg/g protein
mg/100 kcal
1
Cysteine
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21
38
2
Histidine
141
23
41
3
Iso-leucine
...
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51
92
4
Leucine
586
94
169
5
Lysine
...
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63
114
6
Methionine
85
14
24
7
Phenylalanine
...
...
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45
81
8
Threonin2
268
43
77
9
Tryptophan
...
...
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18
33
10
Tyrosine
259
42
75
11
Valine
...
...
...
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50
90
LIST OF METHODS FOR TESTING INFANT FORMULA
I. Protein
1. TCVN 8099-5:2009 (ISO 8968-5:2001) Milk -- Determination of nitrogen content -- Part 5: Determination of protein-nitrogen content
2. TCVN 8100:2009 (ISO 14891:2002) Milk and milk products -- Determination of nitrogen content -- Routine method using combustion according to the Dumas principle
3. AOAC 960.48 Protein Efficiency Ratio
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4. TCVN 6688-1:2007 (ISO 8262-1:2005) Milk products and milk-based foods -- Determination of fat content by the Weibull-Berntrop gravimetric method (Reference method) -- Part 1: Infant foods
5. TCVN 7084:2002 (ISO 1736:2000) Dried milk and dried milk products -- Determination of fat content -- Gravimetric method (Reference method)
6. AOAC 996.06 Fat (Total, Saturated, and Unsaturated) in Foods. Hydrolytic Extraction Gas Chromatographic Method
7. ISO 23065:2009 Milk fat from enriched dairy products – Determination of omega-3 and omega-6 fatty acid content by gas-liquid chromatography
8. AOAC 992.25 - Linoleic Acid in Ready-To-Feed Milk-Based Infant Formula. Gas Chromatographic Method
III. Carbohydrates
9. AOAC 986.25 Proximate Analysis of Milk-Based Infant Formula
IV. Vitamins
10. EN 12823-1:2000 Foodstuffs – Determination of vitamin A by high performance liquid chromatography – Part 1: Measurements of all-trans-retinol and 13-cis-retinol
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12. AOAC 974.29 Vitamin A in Mixed Feeds, Premixes, and Human and Pet Foods. Colorimetric Method
13. AOAC 941.15 Carotene in Fresh Plant Materials and Silages. Spectrophotometric Method
14. AOAC 992.06 Vitamin A (Retinol) in Milk-Based Infant Formula. Liquid Chromatographic Method
15. AOAC 992.04 Vitamin A (Retinol Isomers) in Milk and Milk-Based Infant Formula. Liquid Chromatographic Method
16. EN 12821:2009 Foodstuffs – Determination of vitamin D by high performance liquid chromatography – Measurement of cholecalciferol (D3) or ergocalciferol (D2)
17. AOAC 936.14 Vitamin D in Milk, Vitamin Preparations, and Feed Concentrates
18. AOAC 995.05 Vitamin D in Infant Formulas and Enteral Products. Liquid Chromatographic Method
19. AOAC 992.26 Vitamin D3 (Cholecalciferol) in Ready-To-Feed Milk-Based Infant Formula. Liquid Chromatographic Method
20. TCVN 8276:2010 (EN 12822:2000) Foodstuffs - Determination of vitamin E by high performance liquid chromatography - Measurement of α-, β-, γ- and δ-tocopherols
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22. AOAC 992.03 Vitamin E Activity (All-rac--Tocopherol) in Milk-Based Infant Formula. Liquid Chromatographic Method
23. EN 14148:2003 Foodstuffs – Determination of vitamin K1 by HPLC
24. AOAC 999.15 Vitamin K in Milk and Infant Formulas. Liquid Chromatographic Method
25. AOAC 992.27 trans-Vitamin K1 (Phylloquinone) in Ready-To-Feed Milk-Based Infant Formula. Liquid Chromatographic Method
26. TCVN 5164:2008 (EN 14122:2003) Foodstuffs - Determination of vitamin B1 by high performance liquid chromatography (HPLC)
27. AOAC 942.23 Thiamine (Vitamin B1) in Human and Pet Foods. Fluorometric Method
28. AOAC 986.27 Thiamine (Vitamin B1) in Milk-Based Infant Formula. Fluorometric Method
29. EN 14152:2003 Foodstuffs – Determination of vitamin B2 by HPLC
30. AOAC 970.65 Riboflavin (Vitamin B2) in Foods and Vitamin Preparations. Fluorometric Method
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31. AOAC
985.34 Niacin and Niacinamide (Nicotinic Acid and Nicotinamide)
in Ready-to-Feed Milk-Based Infant Formula. Microbiological-Turbidimetric
Method
33. AOAC
944.13 Niacin and Niacinamide (Nicotinic Acid and Nicotinamide)
in Vitamin Preparations. Microbiological Methods
34. AOAC 961.14 Niacin and Niacinamide in Drugs, Foods, and Feeds. Colorimetric Method
35. EN 14164:2008 Foodstuffs – Determination of vitamin B6 by HPLC
36. EN 14166:2009 Foodstuffs – Determination of vitamin B6 by microbiological assay
37. EN 14663:2005 Foodstuffs – Determination of vitamin B6 (including its glycosylated forms) by HPLC
38. AOAC 961.15 Vitamin B6 (Pyridoxine, Pyridoxal, Pyridoxamine) in Food Extracts. Microbiological Method
39. AOAC 985.32 Vitamin B6 (Pyridoxine, Pyridoxal, Pyridoxamine) in Ready-to-Feed Milk-Based Infant Formula. Microbiological Method
40. AOAC 986.23 Cobalamin (Vitamin B12 Activity) in Milk-Based Infant Formula. Turbidimetric Method
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42. AOAC 992.07 Pantothenic Acid in Milk-Based Infant Formula. Microbiological Turbidimetric Method
43. AOAC 945.74 Pantothenic Acid in Vitamin Preparations. Microbiological Methods
44. EN 14131:2003 Foodstuffs – Determination of folate by microbiological assay
45. AOAC 992.05 Folic cid (Pteroylglutamic Acid) in Infant Formula. Microbiological Methods
46. AOAC 944.12 Folic Acid (Pteroylglutamic Acid) in Vitamin Preparations. Microbiological Methods
47. EN 14130:2003 Foodstuffs – Determination of vitamin C by HPLC
48. AOAC 985.33 VitaminC(Reduced Ascorbic Acid) in Ready-to-Feed Milk-Based Infant Formula. 2,6-Dichloroindophenol Titrimetric Method
49. AOAC 967.22 Vitamin (Total) in Vitamin Preparations. Microfluorometric Method
50. AOAC 984.26 VitaminC(Total) in Food. Semiautomated Fluorometric Method
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V. Minerals and trace elements
52. TCVN 8126:2009 Foods. Determination of lead, cadmium, zinc, copper, and iron. Atomic absorption spectrophotometry after microwave digestion (AOAC 999.10)
53. AOAC 984.27 Calcium, Copper, Iron, Magnesium, Manganese, Phosphorus, Potassium, Sodium, and Zinc in Infant Formula. Inductively Coupled Plasma Emission Spectroscopic Method
54. AOAC 985.35 Minerals in Infant Formula, Enteral Products, and Pet Foods. Atomic Absorption Spectrophotometric Method
55. TCVN 6269:2008 (ISO 8070:2007) Milk and milk products -- Determination of calcium, sodium, potassium and magnesium contents -- Atomic absorption spectrometric method
56. TCVN 6838:2001 (ISO 12081:1998) Milk -- Determination of calcium content -- Titrimetric method
57. TCVN 6271:2007 (ISO 9874:2006) Milk -- Determination of total phosphorus content -- Method using molecular absorption spectrometry
58. AOAC 986.24Phosphorus in Infant Formula and Enteral Products. Spectrophotometric Method
59. AOAC 976.25 Sodium in Foods for Special Dietary Use. Ion Selective Electrode Method
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61. TCVN 7080:2002 (ISO 14378:2000) Milk and dried milk -- Determination of iodide content -- Method using high-performance liquid chromatography
62. EN 15111:2007 Foodstuffs – Determination of trace elements – Determination of iodine by ICP-MS (inductively coupled plasma mass spectrometry)
63. AOAC 992.24 Iodide in Ready-To-Feed Milk-Based Infant Formula. Ion-Selective Electrode Method
64. EN 14627:2005 Foodstuffs – Determination of trace elements – Determination of total arsenic and selenium by hydride generation atomic absorption spectrometry (HGAAS) after pressure digestion
65. AOAC 986.15 Arsenic, Cadmium, Lead, Selenium, and Zinc in Human and Pet Foods. Multielement Method
66. AOAC 974.15 Seleniumin Human and Pet Food. Fluorometric Method
67. TCVN 7086:2007 (ISO 5738:2004) Milk and milk products -- Determination of copper content -- Photometric method (Reference method)
68. TCVN 6841:2001 (ISO 11813:1998) Milk and milk products -- Determination of zinc content -- Flame atomic absorption spectrometric method
69. TCVN 7929:2008 (EN 14083:2003) Foodstuffs - Determination of trace elements - Determination of lead, cadmium, chromium and molybdenum by graphite furnace atomic absorption spectrometry (GFAAS) after pressure digestion
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70. AOAC 999.14 Choline in Infant Formula and Milk Enzymatic Colorimetric Method
71. AOAC 991.39 Fatty Acids in Encapsulated Fish Oils and Fish Oil Methyl and Ethyl Esters. Gas Chromatographic Method
VII. Fluoride
72. AOAC 944.08 Fluorine in Food. Distillation Method
73. AOAC 961.16 Microchemical Determination of Fluorine. Titrimetric Method
VIII. Contaminants
74. TCVN 7602:2007 Foodstuff – Determination of lead content by atomic absorption spectrophotometric method
75. TCVN 7933:2009 (ISO/TS 6733:2006) Milk and milk products -- Determination of lead content -- Graphite furnace atomic absorption spectrometric method
76. TCVN 7788:2007 Canned foods - Determination of tin content by atomic absorption spectrophotometric method
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78. ISO 15495:2010 Milk, milk products and infant formulae – Guidelines for the quantitative determination of melamine and cyanuric acid by LC-MS/MS
79. TCVN 6685:2009 (ISO 14501:2007) Milk and milk powder -- Determination of aflatoxin M1 content -- Clean-up by immunoaffinity chromatography and determination by high-performance liquid chromatography
80. TCVN 7785:2007 (ISO 14674:2005) Milk and milk powder - Determination of aflatoxin M1 content - Clean-up by immunoaffinity chromatography and determination by thin-layer chromatography
81. TCVN 7700-1:2007 (ISO 11290-1:1996, With Amd 1:2004) Microbiology of food and animal feeding stuffs -- Horizontal method for the detection and enumeration of Listeria monocytogenes -- Part 1: Detection method
82. TCVN 7850:2008 (ISO/TS 22964:2006) Milk and milk products -- Detection of Enterobacter sakazakii
83. TCVN 5518-1:2007 (ISO 21528-1:2004) Microbiology of food and animal feeding stuffs -- Horizontal methods for the detection and enumeration of Enterobacteriaceae -- Part 1: Detection and enumeration by MPN technique with pre-enrichment
;
Thông tư 20/2012/TT-BYT về Quy chuẩn kỹ thuật quốc gia đối với sản phẩm dinh dưỡng công thức cho trẻ đến 12 tháng tuổi do Bộ trưởng Bộ Y tế ban hành
Số hiệu: | 20/2012/TT-BYT |
---|---|
Loại văn bản: | Thông tư |
Nơi ban hành: | Bộ Y tế |
Người ký: | Nguyễn Thanh Long |
Ngày ban hành: | 15/11/2012 |
Ngày hiệu lực: | Đã biết |
Tình trạng: | Đã biết |
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