Who We Are
The UK, Ireland, and the wider European Union (EU) and European Economic Area (EEA) remain global hubs for pharmaceutical innovation, biotechnology research, advanced therapies, medical technology, and digital health. Successfully operating across these diverse markets requires navigating evolving regulatory frameworks, market access requirements, quality expectations, emerging technologies, and commercialisation challenges. Organisations must balance local market needs with broader European requirements while maintaining compliance, accelerating innovation, and delivering value throughout the product lifecycle.
PLG UK & Ireland helps life sciences companies transform these challenges into opportunities through integrated support across regulatory affairs, quality, digital quality, safety, clinical development, market access, and lifecycle management.
Whether you are launching products, expanding operations, establishing a local presence, or managing post-approval obligations, or implementing quality digital solutions, we provide practical expertise that helps you move faster and operate with confidence.
Who We Support
We provide support across a broad range of regulated healthcare products and sectors, helping clients navigate complex requirements throughout the product lifecycle, including:
- Human Medicines
- Veterinary Medicines
- Herbal Medicines
- Medical Devices
- Biological Products
- Biocides
- Borderline Products
- Cosmetics
- Food Supplements
This immediately tells visitors that your expertise extends far beyond traditional pharmaceuticals.
Licensed Capabilities
Our clients benefit from working with a partner that holds key UK and European authorisations, enabling us to provide practical operational support alongside strategic consulting services.
Our licences include:
- MIA (Manufacturer's/Importer's Authorisation)
- MIA (IMP)for importation into Europe
- ManA(Manufacturer's Authorisation for Veterinary Medicines)
- WDA(Wholesale Distribution Authorisation)
- CD Licence(Controlled Drug Licence)
- VIA(Veterinary Import Authorisation)
These authorisations enable us to support manufacturing, importation, distribution, controlled drug management, and veterinary product activities across the UK and European markets.
Local Services
A complete set of local services for life science companies that we can scale globally.
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Regulatory Affairs
- Regulatory strategy and planning
- Product registrations and submissions
- Post-approval lifecycle management
- UK and Ireland market entry support
- Regulatory intelligence and compliance
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Quality & Compliance
- Quality management systems
- GMP, GDP, and GCP compliance
- Inspection readiness and remediation
- Audits and supplier qualification
- Quality oversight and governance
- Computerised System
- Validation/Computer Software
- Quality Operational Excellence
- Global Audit Program
- Data Integrity Program
- QMS Performance Improvement
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Safety & Vigilance
- Pharmacovigilance services
- Medical device vigilance
- Risk management activities
- Safety reporting and operations
- Benefit-risk monitoring
- QPPV
- UK Local Contact for PV
- Audits
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Clinical & Development Support
- Clinical development support
- Regulatory documentation
- Clinical trial compliance
- Scientific and operational consulting
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Market Access & Commercial Excellence
- Pricing and reimbursement support
- Market access strategy
- Evidence generation planning
- Product launch readiness
- Commercial support services
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Digital & Transformation Services
- Process optimization
- Regulatory and quality digital solutions
- Data governance and compliance
- Operational transformation initiatives
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Local Affiliate & Outsourcing Services
- Local affiliate support
- Responsible person and local representation services
- Outsourced operational support
- End-to-end lifecycle management
Why Work With PLG UK & Ireland?
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Navigate an Evolving Healthcare Landscape with Confidence
Stay ahead of evolving regulatory requirements, quality expectations, market access challenges, and emerging technologies with practical guidance from experts who actively contribute to industry groups such as ISPE GAMP and bring deep experience across the UK, Ireland, EU, and EEA life sciences landscape.
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Access the Expertise You Need When You Need It
Access a multidisciplinary team of experts across regulatory affairs, quality, pharmacovigilance, clinical development, digital transformation, and market access. Through active participation and leadership in industry organisations such as ISPE GAMP, our specialists provide practical, up-to-date guidance without the complexity of managing multiple service providers.
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Accelerate Development, Approval, and Commercial Success
Move products forward more efficiently through coordinated support that reduces delays, streamlines processes, and improves cross-functional alignment.
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Reduce Risk While Maintaining Compliance
Protect your organization and products through proactive support that helps you meet regulatory obligations, maintain quality standards, and navigate change with confidence.
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Scale Resources to Match Your Business Goals
Whether you need strategic consulting, project-based support, managed services, or full outsourcing, our flexible engagement models help you adapt as priorities evolve.
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Benefit from Local Expertise Backed by Global Capabilities
Leverage deep expertise in the UK, Ireland, EU, and EEA healthcare and life sciences landscape while benefiting from ProductLife Group's global network of specialists, integrated capabilities, and proven best practices across the product lifecycle.
Supporting Success Across the UK, Ireland, and Beyond
Whether you're launching a new product, expanding into new markets, or managing ongoing compliance requirements, our PLG UK & Ireland team helps simplify complexity and accelerate progress.
By combining local market insight with global capabilities, we help clients reduce risk, improve efficiency, and bring innovative healthcare solutions to patients faster.
Local expertise. Global capabilities. A trusted partner for every stage of your product lifecycle.
Integrity
Callisto Pharma Group
Through ProductLife Group's integrated network, clients can access expertise across regulatory affairs, safety, quality, clinical development, digital transformation, commercialization, and lifecycle management through regional and global centers of excellence.
Callisto Pharma Group EU Office
Office 107, Regus Block 1, Blanchardstown Corporate Park, Dublin, Ireland, D15 AKK1
Callisto Pharma Group UK Office
5 Garden Court, Lockington Hall, Main Street, Lockington, DE74 2RH