Chemical-technical products

The product shall not be classified with the following hazard classifications and hazard statements in accordance with Regulation (EC) No.1272/2008 on classification, labelling and packaging of substances and mixtures (CLP regulation), neither in EU-harmonised classification (in accordance with appendix VI in the CLP-regulation), nor in  self-classification.

Exceptions:

Laundry detergents for professional use where the classification with hazard statement H410, H411 or H412 depends on the content of peracetic acid (Cas No 79-21-0) or hydrogen peroxide (Cas No 7722-84-1).

Ingredient substances¹ shall not be classified with the following hazard class and hazard statements in accordance with Regulation (EC) No 1272/2008 on classification, labelling and packaging of substances and mixtures (CLP regulation), neither in EU-harmonised classification (in accordance with appendix VI in the CLP regulation) nor in self-classification.

1272/2008 on classification, labelling and packaging of substances and mixtures (CLP Regulation).

Exemption:

Enzymes (including stabilizers and preservatives in the enzyme raw material). 

Ingredient¹ preservatives and colouring agents shall not be bioaccumulative, in accordance with Regulation (EC) No 1272/2008 on classification, labelling and packaging of substances and mixtures (CLP regulation).

Exceptions:

• Colouring agents approved as food additives in accordance with Regulation (EC) No 1333/2008 on food additives
• Preservatives with LC50, EC50 and IC50 > 100 mg/l or NOEC/ECx > 10 mg/l.
• Readily biodegradable preservatives whose degradation products have BCF or log Kow that fulfils the requirement.
• Preservatives that are not bioavailable (molar mass >700 g/mole)

Surfactants in the products shall be readily biodegradable (aerobic) according to OECD's guidelines test methods 301(A to F) or 310 or similar test methods  and anaerobically biodegradable according to OECD's guidelines test method 311  or similar test methods.

The product shall not be classified with the following hazard class and hazard statements in accordance with Regulation (EC) No 1272/2008 on classification, labelling and packaging of substances and mixtures (CLP regulation), neither in EU-harmonized classification (in accordance with appendix VI in the CLP regulation) nor in self-classification.

The product shall also not be subject to labelling requirements with the text "Contains (the name of the sensitizing substance). May cause an allergic reaction” (EUH208) according to Regulation (EC) No 1272/2008 on classification, labeling and packaging of substances and mixtures (CLP Regulation).

Exceptions:

Products where the labelling with EUH 208 is caused by the classification of the ingredient enzymes.

Concentrated detergents that are diluted at least 10 times with water by the user to the finished product if the user does not come into contact with the product during dilution.

Ingredient substances¹ shall not be classified with the following hazard class and hazard statements in accordance with Regulation (EC) No 1272/2008 on classification, labelling and packaging of substances and mixtures (CLP regulation), neither in EU-harmonised classification (in accordance with appendix VI in the CLP regulation) nor in self-classification.

1272/2008 on classification, labeling and packaging of substances and mixtures (CLP Regulation).

Exceptions:

• Enzymes (including stabilizers and preservatives in the enzyme raw material).
• Preservatives in liquid products included with less than 0,02 weight%

The product shall not contain¹ phosphates.

To be awarded points or price deduction in the evaluation of the bid, the supplier shall confirm in the bid that palm oil, palm kernel oil, palm oil derivatives or palm kernel oil derivatives are produced according to:

• Roundtable on Sustainable Palm Oil (RSPO)¹ or similar system, or
• Council Regulation (EC) nr 834/207 on organic production and labelling of organic products and repealing

Exemption:

Ingoing raw materials in the product  less than 1 percent.

Ingredient substances¹ shall not be classified with the following hazard class and hazard statements in accordance with Regulation (EC) No 1272/2008 on classification, labelling and packaging of substances and mixtures (CLP regulation), neither in EU-harmonised classification (in accordance with appendix VI in the CLP regulation) nor in self-classification.

Exceptions:

• For classification with acute toxicity and/or specific target organ toxicity, the following are exempted:

Enzymes (including stabilizers and preservatives in the enzyme raw material).

Fragrances

Colouring agents approved as food additives in accordance with Regulation (EC) No 1333/2008 on food additives.

Biological substances², for example plant extracts

• For classification with H351, the following are exempted:

Pollutants of NTA (Trisodium nitrilotriacetate, CAS 5064-31-3) in complexing agents at levels of up to 0.1 weight percent in the end product.

EDTA (CAS 60-00-4) shall not be ingredient¹ in the product in concentrations above 0.2 weight percent.

The following substances and substance groups shall not be ingredients¹ in the product:

• Alkylphenolethoxylates (APEOs )
• Organic chlorinated substances and hypochlorite's
• Substances evaluated by EU to be
• Substances evaluated by the EU to be PBT (persistent, bioaccumulative and toxic) or vPvB (very persistent and very bioaccumulative)²
• Substances on the Candidate list³
• Substances that are considered to be endocrine disruptors or potential endocrine disruptors⁴

Exception:

Organic chlorinated substances may be included in preservatives used in dishwasher detergents for professional use.

The product shall not be intended to have antimicrobial function, i.e it may only contain biocides in order to preserve the product or the raw material in the product.

For products with manual dosing, the dosage instructions shall appear on the packaging or the product sheet.

Primary packaging, closures and labels shall fulfill the following:

• The primary packaging¹ and closure² shall be made from one of the following plastics:

Polyethylene (PE)
Polypropylene (PP)
Polyethylene terephthalate (PET)

• The label shall not be made from PS (polystyrene) or halogenated plastics.
• Black primary packaging¹ shall not be coloured with Carbon black.

Exemption

Thermoplastics and rubber parts in closures.

Liners are exempted if they are easily separated from the packaging or closure.

Plastic parts in spray or pump nozzles or dosing systems.

Pouches.

To be awarded [points or price deduction] in the evaluation of the bid, the supplier shall confirm that the pouches used as packaging, in the bid, fulfils the following:

• The primary packaging¹ of laminate is made of:

monomaterial (PE, PP eller PET)

• The closure² is made of one of the following plastics:

Polyethylene (PE)
Polypropylene (PP)
Polyethylene terephthalate (PET)

• The label is not made from PS (polystyrene) or halogenated plastics.
• Black primary packaging¹ and closures are not coloured with Carbon black.
• Fillers (such as CaCO₃) can not be included in PE or PP packaging1 and closures² at a level that the density of the plastic exceeds 0.995g / cm³.
• Barrier coatings can only be made from EVOH (Ethylene vinyl alcohol) in maximum amounts of 2 percent related to the total weight.

Exception:

For cleaning products, pouches with closed-system automatic dosing are exempted.

Any perfumes¹ shall be produced in accordance with the International Fragarance Associations (IFRA² )standards or equivalent.

• The following compounds shall not be added to the product:

Nitromusk compounds and polycyclic musk compounds

Hydroxyisohexyl 3-Cyklohexene Carboxaldehyde, HICC (CASnr 31906-04-4, 51414-25-6)

Atranol (CASnr 526-37-4)

Chloroatranol (CASnr 57074-21-2)

• The following compounds may be added to the product with a maximum of 0,01 weight%:

Fragrances classified as sensitizing with H317

Fragrances that shall be declared according to Regulation (EC) No 648/2004 on detergents

The product shall not contain perfumes, i.e. substances/substance mixtures that are added with the purpose to improve product's fragrance characteristics.

For all products in the contract where safety data sheets are required in accordance with regulation (EC) No 1907/2006 concerning the Registration, Evaluation, Authorisation and Restriction of Chemicals (Reach-regulation), from the start of the contract the supplier shall make sure that:

• safety data sheets are freely available and downloadable in Swedish for the customer via the contractor's website or
• safety data sheets are provided in electronic form in Swedish, i.e. by email in PDF format or similar

The supplier of the products delivered according to the contract shall have routines for systematic quality work. The routines shall be documented, at least include the activities covered by the contract and shall be applied during the contract period. The systematic quality work shall include at least the following points:

• Routines for the requirements in the contract to be controlled and fulfilled during the contract period.
• Routines for the documentation that verifies fulfilment of the requirements are to be available.
• Routines for reporting and processing of deviations related to the set requirements.
• Routines for reporting, documentation and management of claims and complaints regarding the products
• Routines for traceability upstream in the supplier chain for the products covered by the contract.
• That there is a contact person with respect to the contracting authority.
• Routines for the contact person's annual reporting of the above points to the contracting authority

Upon request, the supplier shall be able to prove that the requirement has been met. If the supplier applies its own documented system, [The contracting organization] may request that the information is verified by an independent third party.

1. The supplier's obligation 

Throughout the entire contract period, the supplier shall apply the contract terms under item 1-4. The contract shall be fulfilled in accordance with the following terms regarding workers’ rights:

• The eight core conventions of ILO regarding forced labour, child labour, discrimination, freedom of association, and the right to collective bargaining (no. 29, 87, 98, 100, 105, 111, 138, and 182).

The terms regarding workers’ rights are called “the Terms” hereafter.

In the event of the core conventions of the ILO are in conflict with national law, the supplier shall take reasonable measures to ensure compliancy with the international regulations.

The obligations concerns workers when they perform work within the frame of the contract.

The supplier shall, according to item 2, ensure that the Terms are fulfilled by hired subcontractors that directly contribute to the performance of the contract, regardless of the number of intermediaries. In addition, the supplier shall ensure that these subcontractors participate in the follow-up,
according to item 3.

The obligations concerns work carried out under such conditions where Swedish labour law is not applicable.

2. Policies and routines

To fulfil the obligations under item 1, the supplier shall take measures to prevent and manage any deviations from the Terms according to item 2.1-2.6 below. The measures shall be documented and applied throughout the entire contract period in their own operation and the operation of any subcontractors who directly contribute to the performance of the contract, regardless of the number of intermediaries.

At the start of the contract the supplier shall have:

2.1 adopted a commonly accessible policy, adopted by the highest management including a commitment to respect the Terms,

2.2. adopted routines to convey their commitment to respect the Terms in their own operation and in the supply chain,

2.3 appointed a manager at the highest management level, responsible for compliance with the Terms,

2.4 adopted routines to regularly carry out risk analyses, i.e. to identify and prioritise current and potential risks of deviation from the Terms, as well as mapping the supply chain with special regard to high risk operations,

2.5 adopted routines for regular follow-up of the Terms compliance, and

2.6 adopted routines to immediate action to prevent and limit deviations from the Terms, and to make amendments to identified deviations.

The measures shall be taken in accordance with the UN Guiding Principles on Business and Human Rights, or the equivalent.

3. Follow-up

[The contracting authority] has the right to follow-up that the supplier fulfils its obligations. The follow-up may be carried out in different steps; self-assessment and audit.

3.1 Self-assessment
Upon request from [the contracting authority] the supplier shall, [within six (6) weeks/other time period, specified by the contracting authority] from the receipt of the request, report compliance with the Terms in writing. The account can be submitted by form, according to appendix 1: self-assessment questionnaire. The supplier is expected to provide the information requested in the appendix.

3.2 Audit
The supplier shall enable [the contracting authority] to perform audits, on their own or through a representative, with the supplier and/or its subcontractors to ensure that the supplier fulfils the obligations according to item 1 and complies with the Terms. The supplier shall provide the information and documentation necessary in connection with the audit

4. Management of deficiencies

If the supplier does not participate in follow-up or if there are deficiencies in the documentation to be provided under item 3, a correction shall be made within the time determined by [the contracting authority].

In case of deficiencies in compliance to the Terms, the supplier shall amend this according to a schedule and action plan, developed by the supplier, and to be approved by [the contracting authority]. The schedule and action plan are to be developed within the time period decided by [the contracting authority] and must be proportionate to the nature of the deficiencies and clearly describe how these are to be remedied within the established schedule.

[The contracting authority] has the right to terminate the contract with immediate effect if the supplier do not make amendments within the established period or do not remedy deficiencies within the established
schedule.

[The contracting authority] has the right to terminate the contract with immediate effect in the case of severe deviations from the Terms.

1. The supplier’s obligation

Throughout the entire contract period, the supplier shall apply the contract terms under item 1-4. The contract shall be fulfilled in accordance with the following terms regarding human rights, workers’ rights, environmental protection, and anti-corruption (sustainable supply chains):

• the UN Universal Declaration on Human Rights,
• the UN Convention on the Rights of the Child, Article 32,
• the eight core conventions of the ILO regarding forced or compulsory labour, child labour, discrimination, as well as freedom of association and the right to collective bargaining, (no 29, 87, 98, 100, 105, 111, 138, and 182),
• the labour law in force in the country were the work is performed, including regulations for salary, working hours, leisure time, and work environment,
• the environmental law in force in the country were the work is performed, and
• the UN Convention against Corruption.

The terms regarding sustainable supply chains are called “the Terms”  hereafter.

When international regulations prescribe a stronger protection for the individual than the national legislation, the supplier shall take reasonable measures to ensure compliancy with the international regulations.

The obligations concerns all operations connected to the performance of the contract.

The supplier shall, according to item 2, ensure that the Terms are fulfilled by hired subcontractors in all parts of the supply chain. In addition, the supplier shall ensure that these subcontractors participate in the follow-up, according to item 3.

2. Policies and routines

To fulfil the obligations under item 1, the supplier shall take measures to prevent andmanage any deviations from the Terms according to item 2.1-2.6 below. The measures shall be documented and applied concurrently throughout the entire contract period in their own operation as well as in the operation of any subcontractors in all parts of the supply chain.

At the start of the contract the supplier shall have:

2.1 adopted a commonly accessible policy, adopted by the highest management including a commitment to respect the Terms,

2.2. adopted routines to convey their commitment to respect the Terms in their own operation and in the supply chain,

2.3 appointed a manager at the highest management level, responsible for compliance with the Terms,

2.4 adopted routines to regularly carry out risk analyses, i.e. to identify and prioritise current and potential risks of deviation from the Terms, as well as mapping the supply chain with special regard to high risk operations,

2.5 adopted routines for regular follow-up of the Terms compliance, and

2.6 adopted routines to immediate action to prevent and limit deviations from the Terms, and to make amendments to identified deviations.

The measures shall be taken in accordance with the UN Guiding Principles on Business and Human Rights, or the equivalent.

3. Follow-up

[The contracting authority] has the right to follow-up that the supplier fulfils its obligations. The follow-up may be carried out in different steps; self-assessment and audit.

3.1 Self-assessment
Upon request from [the contracting authority] the supplier shall, [within six (6) weeks/other time period, specified by the contracting authority] from the receipt of the request, report compliance with the Terms in writing. The account can be submitted by form, according to appendix 1: self-assessment questionnaire. The supplier is expected to provide the information requested in the appendix.

3.2 Audit
The supplier shall enable [the contracting authority] to perform audits, on their own or through a representative, with the supplier and/or its subcontractors to ensure that the supplier fulfils the obligations according to item 1 and complies with the Terms. The supplier shall provide the information and documentation necessary in connection with the audit.

4. Management of deficiencies

If the supplier does not participate in follow-up or if there are deficiencies in the documentation to be provided under item 3, a correction shall be made within the time determined by [the contracting authority].

In case of deficiencies in compliance to the Terms, the supplier shall amend this according to a schedule and action plan, developed by the supplier, and to be approved by [the contracting authority]. The schedule and action plan are to be developed within the time period decided by [the contracting authority] and must be proportionate to the nature of the deficiencies and clearly describe how these are to be remedied within the established schedule.

[The contracting authority] has the right to terminate the contract with immediate effect if the supplier do not make amendments within the established period or do not remedy deficiencies within the established
schedule.

[The contracting authority] has the right to terminate the contract with  immediate effect in the case of severe deviations from the Terms.

Ingredient substances¹ shall not be classified with the following hazard class and hazard statements in accordance with Regulation (EC) No 1272/2008 on classification, labelling and packaging of substances and mixtures (CLP regulation), neither in EU-harmonised classification (in accordance with appendix VI in the CLP regulation) nor in self-classification.

Exemption:

Enzymes (including stabilizers and preservatives in the enzyme raw material) if they are in liquid form or as encapsulated granules. 

Ingredient¹ preservatives and colouring agents shall not be bioaccumulative, in accordance with Regulation (EC) No 1272/2008 on classification, labelling and packaging of substances and mixtures (CLP regulation).

Exceptions:

• Colouring agents approved as food additives in accordance with Regulation (EC) No 1333/2008 on food additives
• Preservatives with LC50, EC50 and IC50 > 100 mg/l or NOEC/ECx > 10 mg/l.
• Readily biodegradable preservatives whose degradation products have BCF or log Kow that fulfils the requirement.
• Preservatives that are not bioavailable (molar mass >700 g/mole)

Surfactants in the products shall be readily biodegradable (aerobic) according to OECD's guidelines test methods 301(A to F) or 310 or similar test methods and anaerobically biodegradable according to OECD's guidelines test method 311 or similar test methods.

Exemptions from anaerobic biodegradation:

• Emulsifiers and emollients
• Surfactants in toothpaste

Ingredient substances¹ shall not be classified with the following hazard classifications and hazard statements in accordance with Regulation (EC) No. 1272/2008 on classification, labelling and packaging of substances and mixtures (CLP regulation), neither in EU-harmonised classification (according to appendix VI in the CLP regulation) nor in self-classification.

Exceptions:

• Enzymes (including stabilizers and preservatives in the enzyme raw material) if they are in liquid form or as encapsulated granules.
• Tocopherol and tocopherol acetate.
• Amidoamine: max. 0,3 percent as impurity in Cocamidopropyl Betaine (CARB).

To be awarded points or price deduction in the evaluation of the bid, the supplier shall confirm in the bid that palm oil, palm kernel oil, palm oil derivatives or palm kernel oil derivatives are produced according to:

• Roundtable on Sustainable Palm Oil (RSPO)¹ or similar system, or
• Council Regulation (EC) nr 834/207 on organic production and labelling of organic products and repealing

Exemption:

Ingoing raw materials in the product less than 1 weight percent.

Ingredient substances¹ shall not be classified with the following hazard statements in accordance with Regulation (EC) No 1272/2008 on classification, labelling and packaging of substances and mixtures (CLP regulation), neither in EU-harmonized classification (in accordance with appendix VI in the CLP regulation) nor in self-classification.

Exceptions:

• Fluorine compounds in toothpaste and oral care products
• Benzoic acid in soap, creams and lotions. Products in spray form are not excluded.
• Enzymes (including stabilizers and preservatives in the enzyme raw material) if they are in liquid form or as encapsulated granules. The exception does not apply to enzymes in spray products.
• Colouring agents approved as food additives in accordance with Regulation (EC) No 1333/2008 on food additives.
• Biological substances², for example plant extracts

The following substances and substance groups shall not be ingredients¹ in the product:

• EDTA (CAS 60-00-4)
• Substances evaluated by the EU to be PBT (persistent, bioaccumulative and toxic) or vPvB (very persistent and very bioaccumulative)²
• Substances on the Candidate list³
• Substances that are considered to be endocrine disruptors or potential endocrine disruptors⁴

Exception:

EDTA at levels below 0.6 mg / g active content (AC) in solid soap.

The product shall not be intended to have an antimicrobial function, i.e it may only contain biocides in order to preserve the product or the raw material in the product.

Primary packaging, closures and labels shall fulfil the following:

• The primary packaging¹ and closure² shall be made from one of the following plastics:

Polyethylene (PE)
Polypropylene (PP)
Polyethylene terephthalate (PET)

• The label shall not be made from PS (polystyrene) or halogenated plastics.
• Black primary packaging¹ shall not be coloured with Carbon black.

Exemptions:

Thermoplastics and rubber parts in closures.

Liners are exempted if they are easily separated from the packaging or closure.

Plastic parts in spray or pump nozzles or dosing systems.

Pouches.

Toothpaste packaging

To be awarded points or price deduction in the evaluation of the bid, the supplier shall confirm that the pouches used as packaging, in the bid, fulfils the following:

• The primary packaging¹ of laminate is made of:

monomaterial (PE, PP eller PET)

The closure² is made of one of the following plastics:

Polyethylene (PE)
Polypropylene (PP)
Polyethylene terephthalate (PET)

• The label is not made from PS (polystyrene) or halogenated plastics.
• Black primary packaging¹and closures² are not coloured with Carbon black.
• Fillers (such as CaCO₃) can not be included in PE or PP packaging1 and closures² at a level that the density of the plastic exceeds 0.995g / cm³.
• Barrier coatings can only be made from EVOH (Ethylene vinyl alcohol) in maximum amounts of 2 percent related to the total weight.

Any perfumes¹ shall be produced in accordance with the International Fragrance AssociationsIFRA² standards or equivalent.

 Nitromusk compounds and polycyclic musk compounds shall not be added to the product:

The following compounds may be added to the product with a maximum of 0,01 weight percent:

• Fragrances classified as sensitizing with H317
• Fragrances that shall be declared according to Regulation (EC) No 1223/2009 on cosmetic products, in rinse-off products^3.

The following compounds may be added to the product with a maximum of 0,001 weight percent:

• Fragrances that shall be declared according to Regulation (EC) No 1223/2009 on cosmetic products, in leave-on products⁴

The product shall not contain perfumes, i.e. substances/substance mixtures that are added with the purpose to improve product's fragrance characteristics.

Exemption:

Toothpaste intended for children.

The supplier of the products delivered according to the contract shall have routines for systematic quality work. The routines shall be documented, at least include the activities covered by the contract and shall be applied during the contract period. The systematic quality work shall include at least the following points:

• Routines for the requirements in the contract to be controlled and fulfilled during the contract period.
• Routines for the documentation that verifies fulfilment of the requirements are to be available.
• Routines for reporting and processing of deviations related to the set requirements.
• Routines for reporting, documentation and management of claims and complaints regarding the products
• Routines for traceability upstream in the supplier chain for the products covered by the contract.
• That there is a contact person with respect to the contracting authority.
• Routines for the contact person's annual reporting of the above points to the contracting authority

Upon request, the supplier shall be able to prove that the requirement has been met. If the supplier applies its own documented system, [The contracting organization] may request that the information is verified by an independent third party.

1. The supplier's obligation 

Throughout the entire contract period, the supplier shall apply the contract terms under item 1-4. The contract shall be fulfilled in accordance with the following terms regarding workers’ rights:

• The eight core conventions of ILO regarding forced labour, child labour, discrimination, freedom of association, and the right to collective bargaining (no. 29, 87, 98, 100, 105, 111, 138, and 182).

The terms regarding workers’ rights are called “the Terms” hereafter.

In the event of the core conventions of the ILO are in conflict with national law, the supplier shall take reasonable measures to ensure compliancy with the international regulations.

The obligations concerns workers when they perform work within the frame of the contract.

The supplier shall, according to item 2, ensure that the Terms are fulfilled by hired subcontractors that directly contribute to the performance of the contract, regardless of the number of intermediaries. In addition, the supplier shall ensure that these subcontractors participate in the follow-up,
according to item 3.

The obligations concerns work carried out under such conditions where Swedish labour law is not applicable.

2. Policies and routines

To fulfil the obligations under item 1, the supplier shall take measures to prevent and manage any deviations from the Terms according to item 2.1-2.6 below. The measures shall be documented and applied throughout the entire contract period in their own operation and the operation of any subcontractors who directly contribute to the performance of the contract, regardless of the number of intermediaries.

At the start of the contract the supplier shall have:

2.1 adopted a commonly accessible policy, adopted by the highest management including a commitment to respect the Terms,

2.2. adopted routines to convey their commitment to respect the Terms in their own operation and in the supply chain,

2.3 appointed a manager at the highest management level, responsible for compliance with the Terms,

2.4 adopted routines to regularly carry out risk analyses, i.e. to identify and prioritise current and potential risks of deviation from the Terms, as well as mapping the supply chain with special regard to high risk operations,

2.5 adopted routines for regular follow-up of the Terms compliance, and

2.6 adopted routines to immediate action to prevent and limit deviations from the Terms, and to make amendments to identified deviations.

The measures shall be taken in accordance with the UN Guiding Principles on Business and Human Rights, or the equivalent.

3. Follow-up

[The contracting authority] has the right to follow-up that the supplier fulfils its obligations. The follow-up may be carried out in different steps; self-assessment and audit.

3.1 Self-assessment
Upon request from [the contracting authority] the supplier shall, [within six (6) weeks/other time period, specified by the contracting authority] from the receipt of the request, report compliance with the Terms in writing. The account can be submitted by form, according to appendix 1: self-assessment questionnaire. The supplier is expected to provide the information requested in the appendix.

3.2 Audit
The supplier shall enable [the contracting authority] to perform audits, on their own or through a representative, with the supplier and/or its subcontractors to ensure that the supplier fulfils the obligations according to item 1 and complies with the Terms. The supplier shall provide the information and documentation necessary in connection with the audit

4. Management of deficiencies

If the supplier does not participate in follow-up or if there are deficiencies in the documentation to be provided under item 3, a correction shall be made within the time determined by [the contracting authority].

In case of deficiencies in compliance to the Terms, the supplier shall amend this according to a schedule and action plan, developed by the supplier, and to be approved by [the contracting authority]. The schedule and action plan are to be developed within the time period decided by [the contracting authority] and must be proportionate to the nature of the deficiencies and clearly describe how these are to be remedied within the established schedule.

[The contracting authority] has the right to terminate the contract with immediate effect if the supplier do not make amendments within the established period or do not remedy deficiencies within the established
schedule.

[The contracting authority] has the right to terminate the contract with immediate effect in the case of severe deviations from the Terms.

1. The supplier’s obligation

Throughout the entire contract period, the supplier shall apply the contract terms under item 1-4. The contract shall be fulfilled in accordance with the following terms regarding human rights, workers’ rights, environmental protection, and anti-corruption (sustainable supply chains):

• the UN Universal Declaration on Human Rights,
• the UN Convention on the Rights of the Child, Article 32,
• the eight core conventions of the ILO regarding forced or compulsory labour, child labour, discrimination, as well as freedom of association and the right to collective bargaining, (no 29, 87, 98, 100, 105, 111, 138, and 182),
• the labour law in force in the country were the work is performed, including regulations for salary, working hours, leisure time, and work environment,
• the environmental law in force in the country were the work is performed, and
• the UN Convention against Corruption.

The terms regarding sustainable supply chains are called “the Terms”  hereafter.

When international regulations prescribe a stronger protection for the individual than the national legislation, the supplier shall take reasonable measures to ensure compliancy with the international regulations.

The obligations concerns all operations connected to the performance of the contract.

The supplier shall, according to item 2, ensure that the Terms are fulfilled by hired subcontractors in all parts of the supply chain. In addition, the supplier shall ensure that these subcontractors participate in the follow-up, according to item 3.

2. Policies and routines

To fulfil the obligations under item 1, the supplier shall take measures to prevent andmanage any deviations from the Terms according to item 2.1-2.6 below. The measures shall be documented and applied concurrently throughout the entire contract period in their own operation as well as in the operation of any subcontractors in all parts of the supply chain.

At the start of the contract the supplier shall have:

2.1 adopted a commonly accessible policy, adopted by the highest management including a commitment to respect the Terms,

2.2. adopted routines to convey their commitment to respect the Terms in their own operation and in the supply chain,

2.3 appointed a manager at the highest management level, responsible for compliance with the Terms,

2.4 adopted routines to regularly carry out risk analyses, i.e. to identify and prioritise current and potential risks of deviation from the Terms, as well as mapping the supply chain with special regard to high risk operations,

2.5 adopted routines for regular follow-up of the Terms compliance, and

2.6 adopted routines to immediate action to prevent and limit deviations from the Terms, and to make amendments to identified deviations.

The measures shall be taken in accordance with the UN Guiding Principles on Business and Human Rights, or the equivalent.

3. Follow-up

[The contracting authority] has the right to follow-up that the supplier fulfils its obligations. The follow-up may be carried out in different steps; self-assessment and audit.

3.1 Self-assessment
Upon request from [the contracting authority] the supplier shall, [within six (6) weeks/other time period, specified by the contracting authority] from the receipt of the request, report compliance with the Terms in writing. The account can be submitted by form, according to appendix 1: self-assessment questionnaire. The supplier is expected to provide the information requested in the appendix.

3.2 Audit
The supplier shall enable [the contracting authority] to perform audits, on their own or through a representative, with the supplier and/or its subcontractors to ensure that the supplier fulfils the obligations according to item 1 and complies with the Terms. The supplier shall provide the information and documentation necessary in connection with the audit.

4. Management of deficiencies

If the supplier does not participate in follow-up or if there are deficiencies in the documentation to be provided under item 3, a correction shall be made within the time determined by [the contracting authority].

In case of deficiencies in compliance to the Terms, the supplier shall amend this according to a schedule and action plan, developed by the supplier, and to be approved by [the contracting authority]. The schedule and action plan are to be developed within the time period decided by [the contracting authority] and must be proportionate to the nature of the deficiencies and clearly describe how these are to be remedied within the established schedule.

[The contracting authority] has the right to terminate the contract with immediate effect if the supplier do not make amendments within the established period or do not remedy deficiencies within the established
schedule.

[The contracting authority] has the right to terminate the contract with  immediate effect in the case of severe deviations from the Terms.