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    • Regulatory
      • Technical File
      • Risk Management
      • Biological Evaluation
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      • Regulatory Intelligence (RI) Services
    • Quality
      • QMS implementation including ISO 13485 & MDSAP
      • QMS Packages
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      • Clinical Evaluation
      • Performance Evaluation
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    • Medical Device
      • Technical File
      • Risk Management
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      • Regulatory Intelligence
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    • Software as a Medical Device
      • Technical File
      • Risk Management
      • Regulatory Strategy / Market Access
      • Regulatory Intelligence
      • Clinical Evaluation
    • In Vitro Diagnostics
      • Technical File
      • Risk Management
      • Regulatory Strategy / Market Access
      • Regulatory Intelligence
      • Performance Evaluation for In Vitro Diagnostics
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Category: Uncategorised

Explore Our Supporting Services

LFH Regulatory offers an array of services to meet the diverse needs of our clients. Our comprehensive suite of services includes:

Regulatory

The evolving regulatory landscape, including the Medical Device Regulation 2017/745, makes bringing medical devices to market challenging.
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Technical File

Risk Management

Biological Evaluation

Regulatory Strategy / Market Access

Regulatory Intelligence (RI) Services

Quality

Ensuring quality is essential in the medical device industry. Patient safety, regulatory compliance, and market success all hinge on the quality and consistency of your medical products.
Learn more

We recognise the critical importance of your QMS to your organisation, customers, patients, and regulatory agencies.

Whether you are navigating the complex UK and European markets or expanding your reach globally, our QMS expertise is tailored to meet your specific needs.

QMS implementation including ISO 13485 & MDSAP

Clinical

Clinical and performance evaluations are a vital step in validating the safety and efficacy of your medical devices or IVDs.

Learn more

Clinical Evaluation

Performance Evaluation

Global Registrations

LFH Regulatory provides global registration services to help medical device and In Vitro Diagnostics manufacturers navigate international compliance and market access.
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We can help with everything from feasibility assessment to effective lifecycle management, as well as integrating a robust quality management system into your business operations.

Global registration services

Authorised Representative

LFH Regulatory offers UK Responsible Person and EU Authorised Representative services to ensure compliance with UK MDR 2002 and EU regulations for medical devices.
Learn more

UK Responsible Person Services

EU Authorised Representatives

Training

Understanding Medical Device and In Vitro Diagnostic (IVD) regulations is complex and requires a comprehensive understanding of the entire product lifecycle. 

Learn more
We can help with everything from feasibility assessment to effective lifecycle management, as well as integrating a robust quality management system into your business operations.

Training Solutions

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Simplify your path to compliance, reach out to our experts today!

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  • info@lfhregulatory.co.uk
  • +44 (0)1484 662575

About

  • Homepage
  • About Us
  • Meet The Team
  • Careers
  • Contact Us
  • Homepage
  • About Us
  • Meet The Team
  • Careers
  • Contact Us

Our Services

Regulatory

  • Technical File
  • Risk Management
  • Biological Evaluation
  • Regulatory Strategy / Market Access
  • Regulatory Intelligence (RI) Services

Quality

  • QMS implementation including ISO 13485 & MDSAP
  • QMS Packages

Clinical

  • Clinical Evaluation
  • Performance Evaluation

Authorised Representative

  • UK Responsible Person Services
  • EU Authorised Representatives

Global Registrations

Training

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