Business Details
16 Years
experience
Regulatory Compliance & Testing Services London
Medic Pro is a London-based regulatory affairs consultancy with over a decade of experience supporting businesses in the e-cigarette, cosmetic, biocide, pharmaceutical, and medical device sectors. Founded by a director with extensive pharmaceutical regulation expertise, we specialise in navigating complex compliance frameworks, including EU TPD, UK TRPR, and FDA requirements. Our services encompass product risk assessments, emissions testing, eCTD publishing, and UKAS-accredited laboratory analysis. We prioritise client success through tailored guidance, validated methodologies, and a commitment to staying ahead of evolving regulatory landscapes. With a focus on transparency and technical excellence, we empower clients to achieve market access while maintaining the highest standards of safety and compliance.
Services
TPD Compliance
CBD Testing
eCTD Publishing
CPSR Certification
Biomarker Testing
Medical Device Regulation
PMTA Testing
Product Risk Assessment
Biocides Testing
Novel Food Applications
Details
- Year established: 2010
Highlights and features
- TPD Testing
- TPD compliant
- e-liquid testing lab
Associations and certifications
- UKAS
What people say
Best decision
Extremely easy to work with
Recommend without hesitation
Expert regulatory advice
Timely compliance solutions
Services
TPD Compliance
We provide comprehensive support for EU Tobacco Products Directive compliance, including emissions testing, product notifications, and technical dossier preparation. Our services ensure alignment with MHRA requirements for e-liquid and device manufacturers. Clients benefit from our deep understanding of evolving vape legislation and practical implementation strategies.
CBD Testing
Our ISO 17025-accredited laboratory offers potency testing for CBD and THC content in various product formats. We ensure accurate quantification using validated LC-MS/MS methods, meeting regulatory requirements for legal compliance and consumer safety across UK and EU markets.
CPSR Certification
We deliver Cosmetic Product Safety Reports in accordance with EU Regulation 1223/2009 and UK equivalents. Our qualified assessors evaluate formulations for compliance, covering stability testing, allergen declarations, and packaging compatibility to ensure market readiness.
eCTD Publishing
We specialise in electronic Common Technical Document preparation for FDA, EMA, and MHRA submissions. Our services include dossier formatting, XML backbone creation, and compliance validation to streamline global regulatory approvals for pharmaceutical products.
Medical Device Regulation
We assist with UK MDR and EU MDR requirements, including technical file preparation, UK Responsible Person services, and conformity assessment procedures. Our expertise covers classification, clinical evaluation, and post-market surveillance requirements for device manufacturers.
People
Matt Taylor
Director
Matt founded Medic Pro after a decade in pharmaceutical regulation, expanding expertise to vape, cosmetic, and medical device sectors. He leads regulatory strategy and technical operations, leveraging deep industry knowledge to solve complex compliance challenges for global clients.
Questions
What is TPD compliance for vape products?
TPD compliance requires emissions testing and ingredient disclosure for e-cigarettes under EU and UK regulations, ensuring product safety and regulatory approval through MHRA notifications.
How do I get CPSR certification for cosmetics?
Submit formulation details and test reports to a qualified assessor who will prepare a Cosmetic Product Safety Report confirming compliance with EU and UK cosmetic regulations.
What testing is required for CBD products?
CBD products require potency testing (CBD/THC content) using ISO 17025-accredited methods, plus stability and safety assessments to meet UK and EU regulatory requirements.
How does eCTD publishing work?
eCTD publishing formats regulatory submissions in XML structure for electronic submission to agencies like FDA and EMA, ensuring compliance with ICH technical requirements.
What are UK medical device regulations?
UK MDR requires technical documentation, clinical evidence, and UK Responsible Person oversight for device market access, with classification determining specific conformity assessment procedures.
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Reviews (3)
M. D. (UK Manufacturer/Distributor)
Sep 01, 2017
Report
Without a doubt, they are an invaluable source of regulatory information. We always make time to hear what they have to say.
Fred (UK importer/retailer)
Sep 01, 2017
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Medic Pro really helped to alleviate the pressure caused by the TPD. We import products from China and getting the necessary assurances [as a result of the TPD] was sometimes difficult. Medic Pro supported us to make sure we were meeting our commitments. They also gave us confidence that whatever compliance issue might arise with their support it could be dealt with.
Were very satisfied with the service and more than happy to recommend them.
Were very satisfied with the service and more than happy to recommend them.
Sam (E-liquid Manufacturer)
Sep 01, 2017
Report
The regulatory support we received over the past 2 years has been fantastic. It has been professional and reliable and the best weve found. From assisting us with the notifications to e-liquid testing theyve helped get us TPD compliant and even saved us money. We will continue to get their advice on all regulatory matters.