About Rose Pharma Solutions
Rose Pharma Solutions is a UK-based pharmaceutical consultancy providing specialist support in regulatory affairs, GMP, GDP, quality systems, and compliance for pharmaceutical, biotechnology, and advanced therapy companies.
We support organisations across the product lifecycle, helping them meet MHRA, UK, EU, and global regulatory requirements with clarity, confidence, and practicality.
Leadership
Rose Pharma Solutions is led by Philip Rose, an experienced pharmaceutical consultant and EU Qualified Person (QP) under permanent EU provisions.
Philip has over 25 years’ experience in the pharmaceutical industry, with senior roles spanning Quality Control (QC), pharmaceutical manufacturing, regulatory compliance, and executive leadership. His background uniquely combines hands-on industry expertise with direct regulatory authority experience, enabling informed, inspection-ready consultancy.
Experience & Regulatory Expertise
Before founding Rose Pharma Solutions, Philip Rose was a Lead Senior GMDP Inspector at the Medicines and Healthcare products Regulatory Agency (MHRA).
He led and conducted GMP and GDP inspections across the UK and internationally, including inspections on behalf of the European Medicines Agency (EMA) and joint inspections with the EMA and the U.S. Food and Drug Administration (FDA).
Philip’s inspection experience covers biological medicinal products (including vaccines), sterile and non-sterile manufacturing, Advanced Therapy Medicinal Products (ATMPs), and UK Specials.
During his time at the MHRA, he was a member of the Compliance Management Team (CMT) and served as Inspectorate Technical Lead for Biological Medicinal Products, having previously held the role for sterile manufacturing.
Philip combines first-hand regulatory authority experience with extensive industry knowledge and is one of the few consultants globally with direct accreditation and operational experience as an EU Inspector specialising in biological and advanced therapy medicinal products.
Recognised Areas of Expertise
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Manufacturing, testing, and distribution of biological, sterile, non-sterile, and advanced therapy medicinal products (ATMPs)
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Specialist cross-contamination audits and mock regulatory inspections
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Global auditing and mock inspection services
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Good Manufacturing Practice (GMP) compliance and implementation
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UK Specials manufacturing oversight and regulatory support
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Training, mentoring, and capability development
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Inspection readiness and post-inspection remediation
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Regulatory compliance and consultancy advice