About Rose Pharma Solutions
Rose Pharma Solutions is a UK-based pharmaceutical consultancy providing specialist support across regulatory affairs, GMP, GDP, quality systems and compliance for pharmaceutical, biotechnology and advanced therapy organisations.
We support organisations throughout the product lifecycle, helping them understand and meet MHRA, UK, EU and international regulatory requirements with clarity, confidence and practical expertise.
At the heart of Rose Pharma Solutions is a unique combination of pharmaceutical industry experience and direct regulatory authority experience.
Philip Rose — Pharmaceutical Consultant & EU Qualified Person
Rose Pharma Solutions is led by Philip Rose, an experienced pharmaceutical consultant and EU Qualified Person (QP)under permanent EU provisions.
Philip has more than 25 years' experience in the pharmaceutical industry, with senior roles spanning Quality Control, pharmaceutical manufacturing, regulatory compliance and executive leadership.
This extensive industry experience, combined with his background as a regulatory inspector, provides a unique perspective on pharmaceutical compliance and regulatory expectations.
Philip Rose's Regulatory Experience
Before founding Rose Pharma Solutions, Philip was a Lead Senior GMDP Inspector at the Medicines and Healthcare products Regulatory Agency (MHRA).
During his time with the MHRA, Philip led and conducted GMP and GDP inspections across the UK and internationally, including inspections carried out on behalf of the European Medicines Agency (EMA) and joint inspections with the EMA and the U.S. Food and Drug Administration (FDA).
His inspection experience covers a broad range of pharmaceutical operations, including biological medicinal products and vaccines, sterile and non-sterile manufacturing, Advanced Therapy Medicinal Products (ATMPs) and UK Specials.
Philip was also a member of the MHRA Compliance Management Team (CMT) and served as Inspectorate Technical Lead for Biological Medicinal Products, having previously held the role for sterile manufacturing.
This combination of first-hand regulatory authority experience and extensive pharmaceutical industry knowledge enables Philip to provide practical, independent and inspection-informed consultancy.
He is also one of the few consultants globally with direct accreditation and operational experience as an EU Inspector specialising in biological and advanced therapy medicinal products.
Specialist Areas of Expertise
Rose Pharma Solutions provides specialist expertise across:
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GMP compliance and implementation
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GMP and GDP inspections
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Regulatory compliance and consultancy
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Inspection readiness and post-inspection remediation
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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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UK Specials manufacturing oversight and regulatory support
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Training, mentoring and capability development
Our approach combines regulator-level insight with practical pharmaceutical industry experience, helping organisations identify risks, understand regulatory expectations and build effective, sustainable approaches to compliance.
