Mastermind Translations

About Mastermind Translations

Mastermind Translations is a specialist language service provider dedicated exclusively to the life science industries. We support high-growth pharmaceutical and medical device companies with regulatory-grade translation services. Our ISO 17100 and ISO 18841 certified processes ensure accuracy, compliance, and timely delivery across all mission-critical content. Trusted by clients across the UK, Europe, and the US, we combine deep industry expertise with a rigorous, detail-focused approach and a personalised service.

 

Translation Support Across the Product Lifecycle
For pharmaceutical and medical device companies entering or operating in the EU:

Research & Development (R&D)
• Patent filings, scientific papers, preclinical and GLP study reports
• Clinical trial protocols, investigator brochures, clinical study reports (CSRs)
• Informed consent forms (ICFs), patient-facing materials, PROs and CRFs
• CMC documents, lab data, and ethics submissions

Regulatory Submission & Approval
• SmPCs, PILs, and labelling using EMA QRD templates
• EU packaging texts and marketing authorisation documentation
• MDR/IVDR technical files, CERs, risk management documentation
• EU Declarations of Conformity, IFUs, GUI content, UDI/DHF documents

Manufacturing & Quality Assurance
• GMP-compliant SOPs, production specifications, validation protocols
• Quality manuals, audit documentation, CAPAs, and inspection reports
• Health & Safety manuals and manufacturing training materials

Post-Market Surveillance & Compliance
• PSURs, RMPs, adverse event reports, and pharmacovigilance documentation
• PMCF reports, vigilance incident reports, and Field Safety Notices (FSNs)

Commercialisation & Stakeholder Communication
• Product brochures, websites, promotional content, and HCP materials
• Sales training documents, educational leaflets, and corporate messaging
• HCP letters, clinical data summaries, and multilingual Q&As