What we do
Quality First International has developed and maintains quality, technical, regulatory and scientific expertise in many areas to assure full support to our clients.
- Biological Safety Programme
- Brexit medical device risk assessment
- CE-Search
- Clinical data and evaluation
- Clinical Evaluation Programme
- Clinical Trials Program
- Corporate Excellence Programme
- EU Authorised Data Protection Representative Programme (EUADPRP)
- Expert Witness Programme
- General services
- Labour Standards Assurance System Programme
- Medical Device Business Segment services
- Medical Device Environmental Waste Management Programme
- Medical device, (Private-label/virtual manufacturing) own brand label manufacture services
- Medical device protection compliance
- Medical device registration services
- Medical device risk assessment
- Medical device single-audit program services
- Medical device software services, including stand-alone software, risk analysis & medical apps
- Microbiology Advisory Program
- Product complaint handling services
- Registar* - Medical Device Registration
- Remedium: Compliance Recovery Programme
- Remedium programme
- Scientific and clinical literature services integrated in CEP
- Specialist services Brexit risk-assessment
- StandardSearch Programme
- Usability and human factors engineering
- Market surveillance
- EU Clinical authorised representative program
- EU Authorised Representative Programme
- UK Responsible Person Programme
- International Representative Program
- United States (US) agent Program
- Official Importer services
- Audits and inspections
- Auditus
- CE Mark Programme
- Classify
- Medical device regulatory support and standards compliance
- Post-market surveillance Programme
- Private label own brand manufacture Programme
- Quality management system
- QMS Advisory service
- US FDA Clearance