Your Authorised Representative for PPE Manufacturers

Assumption of Manufacturer Obligations under PPE Regulation (EU) 2016/425

As an authorised representative for manufacturers of personal protective equipment (PPE), we take on specific tasks defined in Regulation (EU) 2016/425 – ensuring your products can be placed on the EU market in full compliance.

Our Tasks

Perform the following manufacturer obligations under PPE Regulation (EU) 2016/425, Art. 9:

• Keeping the EU declaration of conformity available
• Retaining technical documentation for 10 years
• Submitting documents to market surveillance authorities
• Coordinating translations
• Supporting authorities in official measures

 
Professional certification management

• Coordination with notified bodies
• Administration of certification processes
• Deadline tracking and document management
• Interface between manufacturer and testing body
• Monitoring of certificate validity periods
• Organisation of recertifications
• Management of multiple PPE product lines
  
  

Requirements

• Written authorisation by the manufacturer
• Complete technical documentation
• Valid EU declaration of conformity
• Clear communication channels

Your Benefits

• Legally compliant EU representation for all manufacturers
• Professional certification management
• Single point of contact for authorities and notified bodies
• Risk minimisation during market surveillance

 
PPE manufacturers trust our expertise. We relieve you of administrative burdens, allowing you to focus on your core business.

Note

•  Our authorised representative service includes the legal representation function and administrative coordination of certification procedures only.
• For consulting services on product conformity, please refer to other sections of our website.

How It Works

1. Contact us for a non-binding consultation.
2. We review your documentation.
3. We take on your duties as Authorised Representative.
   
   

Please stop by again. Thank you for your interest!