Sciom, Your UK-Based Strategic Pharmaceutical Partner
Sciom is a UK-based pharmaceutical partner operating within MHRA-approved, GMP-aligned, and ISO-certified frameworks, supporting organisations across the full product lifecycle.
We combine scientific expertise with regulatory rigour to deliver compliant, inspection-ready solutions that protect data integrity, patient safety, and product quality.
- Pharmacovigilance services
- CDMO services
- Regulatory services
- Audit and compliance services
- Validation and Qualification services
Compliant. Certified. Trusted.
Operating to UK and global pharmaceutical standards, Sciom ensures quality, compliance and confidence at every stage.
MIA 58738
GMP 58738/34801864
Holding Schedule 1 - 5
ISO 9001: 2015-GB60393A
Integrated Pharmaceutical Services
Pharmacovigilance Services
- AI-Enabled Safety Platform
- Expert-Led PV Oversight
- Global Inspection-Ready Systems
- Seamless & No Cost Data Migration
- Quality-Driven delivery
- End-to-End Pharmacovigilance Support
CDMO Services
- Full Lifecycle Support (Development to Launch)
- GMP-Compliant End-to-End CDMO Services
- Sterile & Injectable Formulation Development
- Tablets, Suspension & Complex Dosage Forms
- Scalable GMP Manufacturing Support
- Inspection-Ready Quality Systems
Regulatory Affairs Services
- Global Submissions Expertise (IND/NDA/ANDA)
- End-to-End Regulatory Lifecycle Support
- Integrated Medical & Regulatory Writing
- Seamless eCTD Platform
- Proactive Gap Analysis & Risk Mitigation
- Real-Time Regulatory Intelligence
Compliance Management
- Expert-Led Audit Team (QP, QPPV, RP & Lead Auditors)
- Risk-Based Audit Frameworks
- GMP, GDP & PV Audit Expertise
- MHRA & Global Inspection Support
- End-to-End Compliance Assurance
- Patient Safety-Focused Audit Approach
Validation & Qualification
- End-to-End Validation & Qualification Services
- GMP & Regulatory-Compliant Validation Expertise
- Equipment, Process & System Qualification (IQ/OQ/PQ)
- Computer System Validation (CSV) Support
- Risk-Based Validation Approach (QbD Aligned)
- Audit-Ready Validation Documentation
Our Impact
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Years Of Combined Industry Experience
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Products Under Ongoing Management
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Batches Tested and Released
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Countries Covered
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Case Reports Processed Annually
What Makes Sciom
Different
Precision-driven integrated pharmaceutical expertise driven by compliance, AI-enabled innovation, and regulatory excellence, delivering end-to-end support across the entire product lifecycle.
Integrated Partner
Cross-functional expertise across pharmacovigilance, regulatory affairs, CDMO, Compliance, Importation and Validation services under one coordinated structure.
AI-Enabled Solutions
Advanced technology accelerates operations while expert oversight ensures quality and compliance.
Regulatory Excellence
Built-in alignment with global regulatory standards for continuous audit readiness.
Client Visibility
End-to-end traceability from receipt to release through secure, role-based interactive dashboards
Flexible Engagement
Tailored solutions designed to adapt to your organisation's evolving needs.
Insights & Industry Trends
Stay informed with expert commentary on pharmacovigilance services, regulatory consulting services, analytical science and audit compliance services across the pharmaceutical industry.
12 May 2026