Background information: previous EU acts 96/98 are abandoned and new EU act 2014/90 took effect. All marine products to EU must meet the requirement of EU Act 2014/90 since Sep 18, 2016, otherwise Declaration of Conformity cannot be issued, and products might be rejected by EU. Clause 13 of Act 2014/90 says:

　　Non-EU Marine equipment manufacturers must appoint a MED AUTHORIZED REPRESENTITIVE：
　　- Keep related EU conformity declarations and technical documents for more than 10 years based on life cycle of products
　　- Provide all required information and documentation during inspection of authorities in charge
　　- Work with authorities in charge to take due actions to eliminate potential risks of authorized products


McSea provides below service according to the new rules.
　　• Consultation and training for new rules
　　• Guide the manufacturers to issue DOC certificate in right form
　　• Check & record MED certificates for member manufacturer
　　• Present the manufacturers to handle the matters regarding MED certificate at Europe