UK Responsible Person (UKRP) Services by Global Regulatory Services (GRS): Your Trusted Partner for UK Compliance

 

The UK’s regulatory landscape demands precision, expertise, and unwavering compliance. For manufacturers across the life sciences industry, Global Regulatory Services (GRS) ensures seamless market access through our comprehensive UK Responsible Person (UKRP) services. Whether you're in medical devices, pharma, cosmetics, or advanced therapeutics, we’ve got you covered.

 

Our Comprehensive UKRP Services

1. Broad Sector Expertise

GRS proudly serves manufacturers in the following life sciences sub-industries:

• Medical Devices and In Vitro Diagnostics (IVDs)
• Pharmaceuticals and Biologics
• Advanced Therapy Medicinal Products (ATMPs): Cell and gene therapies.
• Cosmetics and Personal Care Products
• Nutraceuticals and Food Supplements
• Veterinary Products
• Digital Health and Software as a Medical Device (SaMD)
• Cannabis-Based Medicinal Products (CBMPs)

2. Ensuring Market Compliance

• Device and Product Registration: We handle the registration of medical devices, pharmaceuticals, IVDs, and more with the MHRA.
• Conformity Verification: GRS ensures your products comply with UK regulations, including UKCA and CE marking (where applicable).
• Technical Documentation Management: We maintain and manage your technical files, declarations of conformity, and certificates to meet MHRA standards.

3. Independent Representation

• Neutral and Objective Support: As an independent UKRP, GRS offers impartial oversight, prioritizing compliance, safety, and market integrity.
• Economic Operator Role: We serve as your designated Economic Operator, bridging regulatory requirements between manufacturers and the MHRA.

4. Comprehensive Post-Market Surveillance

• Complaint Handling: We maintain a complaint register in line with UK reporting standards.
• Incident Reporting: GRS works directly with the MHRA to report and address adverse incidents or risks.
• Corrective Actions: We assist with Preventive and Corrective Actions (CAPA) to resolve compliance issues efficiently.

5. Labelling and Packaging Compliance

• UKRP Identification: GRS ensures its details are included on product labels, packaging, or instructions for use (IFU), as required for UKCA-marked products.
• Verification of Compliance: From labelling to instructions, we ensure that all materials meet UK regulatory standards across all life sciences sub-industries.

 

Why Choose GRS as Your UK Responsible Person?

• Comprehensive Industry Knowledge: We understand the unique regulatory needs of every life sciences sub-industry.
• Proven Expertise: With years of experience in regulatory compliance, GRS ensures your obligations as a manufacturer are met with precision.
• Proactive Compliance: We stay ahead of regulatory changes, ensuring you remain compliant at every stage.
• Global Reach, Local Expertise: While based in the UK, we’re equipped to support manufacturers from all over the world.

 

Take the Next Step with GRS

Whether you're a pharmaceutical innovator, a medical device manufacturer, or a cosmetics company, GRS ensures your products meet all UK regulatory requirements. Let us be your partner in compliance and market success.

📩 Contact Us Today

• Email: grs@globalregulatoryservices.com
• Web Form: Contact GRS

With GRS as your UKRP, your compliance across the life sciences spectrum is in trusted hands.