Taylored Solutions for EU Responsible Person and EU Regulations

Do You Need Support With

  • Complex and Revolving Regulations

  • Documentation and Technical Files

  • Product Labeling and Claims

  • Registration and Approvals

  • Market Access Challenges

  • Quality Control and Product Safety

  • Non-Compliance Resolution

  • Cosmetics, Medical Devices & Food Supplements Regulation

Taylored Consultancy provides expert guidance and tailored regulatory solutions through our certified legal team, working closely with your company to manage documentation and ensure full compliance, making it easy to meet all legal requirements for the medical devices, cosmetics and food supplements

Need Expert Advice?

Let’s Make Compliance Simple

Committed to Compliance Excellence

Food Supplements

Cosmetics

Medical Devices

Why Do I Need A EU Responsible Person? (EURP)

Appointing an EU Authorized Representative is crucial for non-EU manufacturers to ensure the proper preparation and maintenance of essential documents, such as the EU Declaration of Conformity and technical files for medical devices. For companies seeking to import their product(s) into the EU, having an authorized representative is a mandatory requirement.

What Are The EURP Responsibilities?

Regulatory Requirements:

Medical device, food supplements and cosmetics manufacturers intending to import their products into the EU must appoint an EU Authorized Representative. This representative ensures compliance with EU regulations, serves as a point of contact with European authorities, and ensures the accuracy and completeness of all required documentation.

Market Access:

Appointing an EU Authorized Representative goes beyond regulatory compliance—it offers a strategic edge when entering the market. By ensuring your products meet EU standards, we help you establish trust with distributors and customers.

Mitigating Risk:

An EU Authorized Representative plays a key role in risk mitigation by ensuring your products meet EU standards. This helps safeguard against potential legal and financial consequences resulting from non-compliance.

Ongoing Compliance:

After your product enters the market, we ensure your product(s) continue to meet compliance standards. We handle authority requests, provide required documentation, and demonstrate conformity on your behalf.

Ready to Simplify Compliance?

Let us handle the complexities of UK and EU regulations, so you can focus on growing your business.

What Our Clients Say

I am writing to wholeheartedly recommend Bethany, whose collaboration has not only been immensely valuable but truly transformative in our recent project. Bethany stands out as a beacon of professionalism, demonstrating a level of dedication and expertise that is rare and highly commendable. Her dynamic approach to challenges is both refreshing and effective, allowing our team to navigate complexities with confidence. Bethany possesses a unique ability to anticipate the needs of a project, taking informed, proactive steps that ensure success. This foresight, combined with her willingness to take initiative in key decision-making processes, has significantly contributed to our achievements. I highly recommend Bethany, without hesitation!

Sven, Managing Director

Quotation Marks

Taylored Consultancy were clear with direction, great at communicating, and easy to get in contact with.

Jan, Director

Quotation Marks

Working with Taylored Consultancy has brought an additional layer of expertise to our business. Collaborating with Bethany has allowed us to remain compliant, whilst offering practical solutions that help us to clearly and effectively communicate with our customers. From formulations through to consumer-facing claims, Bethany remains a joy to work with, always on hand to expertly offer tailored regulatory advice.

Heather, Head of Marketing

Quotation Marks

Frequently Asked Questions

Not sure about something? Check our FAQ for answers to the most common questions about compliance, documentation, and regulations.

  • We provide end-to-end regulatory solutions, including product registrations, compliance documentation, technical file creation, labeling reviews, marketing claims verification, and appointment of UK/EU Responsible Persons.

  • We specialize in regulatory compliance for medical device manufacturers, cosmetics companies, and food supplement producers.

  • We manage the entire registration process, from documentation preparation to regulatory submissions, approvals and post market compliance.

  • We monitor regulatory updates and changes to ensure our clients’ products remain compliant with the latest requirements.

  • Timelines vary depending on the product type and regulatory body, but we aim to streamline the process and keep you informed every step of the way.

  • Yes, we assist with the implementation of QMS, including ISO 13485, ISO 9001, ISO 22716 and HACCP to ensure product quality and compliance.