EUROLAB European Federation of National Associations of Measurement, Testing and Analytical Laboratories

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EUROLAB European Federation of National Associations of Measurement, Testing and Analytical Laboratories

Transatlantic Trade and Investment Partnership Impact on accreditation and laboratories

What is TTIP? TTIP is the Transatlantic Trade and Investment Partnership agreement currently being negotiated by the EU and US. The future agreement would cover more that 40% of global GDP and account for large shares of world trade and foreign direct investment. TTIP wants to Ease market access for EU companies to the US Cut red tape ( Technical Barriers to Trade ) Put in place new rules for future cooperation 2bn daily Current EU US trade

How did it start? In February 2013, the US President Barack Obama, the European Council President Herman Van Rompuy and the European Commission President José Manuel Barroso announced the launch of the negotiations. A high-standard Transatlantic Trade and Investment Partnership would advance trade and investment liberalization and address regulatory and other non-tariff barriers.

How did it start? Originally the aim was to come to an agreement by the end of 2015. The current goal is to finalise the negotiations while the Obama administration is still in power. Since 2013, 14 negotiating rounds have taken place so far. In November 2014, in an effort to enhance transparency, the new Juncker Commission committed to providing greater access to documents relating to the negotiations. The stakeholders involvement has also gradually increased. In May 2016, Greenpeace leaked textual negotiation proposals for the first time the public could get an idea of the US negotiation position

14th negotiation round in July: Proposals for almost all chapters are now on the table TBT chapter: Text has been consolidated Where are we now? Under discussion: Issues related to the conformity assessment of products How to improve the recognition by one Party of certification carried out in the territory of the other Party on the basis of the requirements of the importing Party What will be the role of respective governmental authorities in the designation and monitoring of the conformity assessment bodies located in their territory The role of the accreditation bodies in evaluating the technical competence of the conformity assessment bodies. Both sides exchanged views on the EU demands for the improvement of the US third party conformity assessment scheme applicable to engineering products (double testing, use of accreditation for the designation of conformity assessment bodies and the possibility to have a common mark to identify compliant products)

TTIP in the news

The Industry View

Next Steps Next negotiation round 3-7 October 2016 US: finalise talks before Obama leaves office in January 2017 Political pressure from the US side US might be willing to take high level political decisions instead of continuing with the more detailed negotiation work EU side does not seem to share this feeling of urgency, is not willing to go for a TTIP Lite and they feel that the negotiations are not yet at a stage were high level political decisions can be made. The US and Italy proposing a Step 1 or TTIP light deal European Commission not willing to agree on TTIP light

Why is TTIP relevant for us? Cutting red tape reducing technical barriers to trade (TBTs) reducing differences in standards and conformity assessment procedures

Why is TTIP relevant for us? Initially, the TTIP negotiators have declared their intention to tackle TBTs through harmonising standards and mutual recognition of conformity assessment results. BUT Mutual recognition requires the same - Conformity assessment methods - Standards - Accreditation requirements Example Consumer Products: SDoC Suppliers Declaration of Conformity 3 rd Party Independent 3 rd Party Certification

Why is TTIP relevant for us? Both the US and the EU have highly sophisticated regulatory systems. But they have very distinct processes and procedures for developing standards and use of conformity assessment modules. These differences arise from material law, standards and standards development procedures, conformity assessment, regulatory, and market authorisation requirements that differ or are not mutually recognised. There is insufficient compatibility between the legal systems and there is no a common institutional framework. The principle of mutual recognition can only be effective when products share common standards and the same, trusted mode of conformity assessment.

Example 1: TTIP and Accreditation Basis for accreditation and conformity assessment in the EU: Regulation (EC) No 765/2008 Key principles: Accreditation is a service of public interest NABs exercise public authority, irrespective of their legal status NABs are not-for-profit organisations NABs are mandated from their national governments and notified to the European Commission One single AB per Member State

Example 1: TTIP and Accreditation The implementation of these principles are of special importance for the operation of the Single Market regulators, stakeholders, CABs, users of conformity assessment services and finally the society may have confidence in accreditation and the conformity assessment principles introduced and applied in European legislation. the principles of Regulation (EC) No 765/2008 should be taken into account when negotiating international trade agreements The requirements established in Regulation 765/2008 are in line with the requirements of ISO / IEC 17011 Conformity Assessment General requirements for accreditation bodies accrediting conformity assessment bodies

Example 1: TTIP and Accreditation The EU is the only economic area where Member States have adopted a common legislation for accreditation in order to support and facilitate trade. This also supports the principle of mutual recognition of accreditations as well as of reports and certificates issued by conformity assessment bodies. In some countries the principles for operating accreditation bodies are not stated in the national legislation but are operated on a voluntary basis in accordance with ISO / IEC 17011 some of the European principles do not apply in the US (e.g. not-for-profit, no competition between accreditation bodies ).

Example 1: TTIP and Accreditation Challenge: In Europe accreditation is the preferred tool for the assessment of competence of CABs European Commission has an interest in introducing the European system of accreditation and conformity assessment when negotiating trade deals If a country operates accreditation on a voluntary basis the EU needs to introduce in the agreement provisions for the recognition of ABs and CABs to ensure that the European accreditation model is not undermined CABs are recognised by the other Party Examples for such provisions are included in CETA, the free trade agreement between the EU and Canada, e.g. Provisions for the accreditation of CABs located in the other Party s territory Provisions for the recognition of ABs

Example 2: TTIP and Conformity Assessment Mutual recognition of conformity assessment results Mutual recognition of conformity assessment results can only occur when products share the same common standards, the methods to establish conformity are the same in both markets and those providing conformity services fulfil the same levels of recognition/accreditation EU US 3 rd party certification 3 rd party certification SDoC SDoC SDoC 3 rd party certification

Example 2: TTIP and Conformity Assessment Comparison SDoC 3 rd party certification

Example 2: TTIP and Conformity Assessment Perception of Conformity Assessment in TTIP EU Textual Proposal for a chapter on TBT, Art. 1: The objective of this Chapter is to promote convergence in regulatory approaches by reducing or eliminating conflicting technical requirements as well as redundant and burdensome conformity assessment requirements. Conformity assessment is not a redundant and burdensome requirement but rather a method to comply with local laws and legal requirements. The legislator must define the appropriate conformity assessment requirements in relation to the potential risk of the product. Compliance with rules and regulations is not an option.

Final considerations A. Legal harmonization and mutual recognition instruments are, in the short or medium term, not appropriate methods to facilitate the removal of existing barriers to trade. B. Assessment bodies at the home location should be authorized to test certain products in accordance with the legal and technical (standard-based) requirements that apply in the other economic area. C. The application of such a national treatment approach would facilitate one-stop shopping for conformity assessment ( Transatlantic Conformity Assessment ) and would achieve a significant facilitation of trade in the context of TTIP through the use of one accreditation body for both markets.

Questions?

International Forum for the Laboratory Community Thank you for you attention!