Farbridge Pharma Consulting
Farbridge Pharma Consulting is a leading expert in GxP Quality Assurance, providing comprehensive consulting, training, staffing, and auditing services to the life sciences industry worldwide. Founded by a European Qualified Person in San Diego, California, the company aims to facilitate seamless access to foreign clinical trials and markets, ensuring compliance with pharmaceutical regulations. Their mission is to deliver tailored GxP Quality Assurance solutions with multilingual support, supporting clients in maintaining high standards of quality and compliance across global markets.
Industries
Nr. of Employees
small (1-50)
Farbridge Pharma Consulting
San Diego, California, United States, North America
Products
US FDA cGMP for Pharmaceuticals & Biotechnology Products (course)
Self-paced online course covering the purpose and fundamentals of cGMP, QMS structure, 21 CFR Parts 210 and 211, regulatory submissions and inspection preparedness; includes a 30-minute one-on-one session with a trainer and a certificate of completion.
Data Integrity in a GMP Environment (course)
Self-paced online training covering ALCOA+ principles, regulatory expectations, data lifecycle management, risk assessment and data integrity controls; includes a 30-minute personalized trainer session and a certificate of completion.
How to be an Effective GMP Auditor (course)
Course focused on auditor skills for GMP environments, delivered online and targeting hands-on auditing competency development; includes course materials and a certificate of completion.
US FDA cGMP for Pharmaceuticals & Biotechnology Products (course)
Self-paced online course covering the purpose and fundamentals of cGMP, QMS structure, 21 CFR Parts 210 and 211, regulatory submissions and inspection preparedness; includes a 30-minute one-on-one session with a trainer and a certificate of completion.
Data Integrity in a GMP Environment (course)
Self-paced online training covering ALCOA+ principles, regulatory expectations, data lifecycle management, risk assessment and data integrity controls; includes a 30-minute personalized trainer session and a certificate of completion.
How to be an Effective GMP Auditor (course)
Course focused on auditor skills for GMP environments, delivered online and targeting hands-on auditing competency development; includes course materials and a certificate of completion.
Services
End-to-end consulting to design, implement or upgrade Quality Management Systems across GxP domains, including documentation, implementation plans and stakeholder coordination.
Conduct quality, due-diligence and for-cause audits as well as mock inspections simulating major regulatory authorities, with auditors experienced in specific technical fields and jurisdictions.
Provide self-paced and instructor-led courses on topics such as cGMP, data integrity, auditor training, leadership and quality culture; courses include certificates and optional individual coaching sessions.
Short-response confidential advisory service where clients submit technical or regulatory questions to GxP experts; responses provided under NDA.
Recruit and supply QA professionals for permanent, temporary or fractional roles; match client projects to consultant expertise and coordinate rapid deployment.
Provide regulatory responsible-person services and oversight to support product release, pharmacovigilance and compliance with local requirements.
End-to-end consulting to design, implement or upgrade Quality Management Systems across GxP domains, including documentation, implementation plans and stakeholder coordination.
Conduct quality, due-diligence and for-cause audits as well as mock inspections simulating major regulatory authorities, with auditors experienced in specific technical fields and jurisdictions.
Provide self-paced and instructor-led courses on topics such as cGMP, data integrity, auditor training, leadership and quality culture; courses include certificates and optional individual coaching sessions.
Short-response confidential advisory service where clients submit technical or regulatory questions to GxP experts; responses provided under NDA.
Recruit and supply QA professionals for permanent, temporary or fractional roles; match client projects to consultant expertise and coordinate rapid deployment.
Provide regulatory responsible-person services and oversight to support product release, pharmacovigilance and compliance with local requirements.
Expertise Areas
- GxP Quality Assurance
- Quality Management System implementation
- Regulatory compliance and inspection readiness (FDA, EMA, MHRA, TGA, ANVISA, NMPA, Health Canada, Swiss Medic)
- Auditing and mock inspections
Key Technologies
- cGMP (current Good Manufacturing Practices)
- GxP frameworks (GMP, GCP, GLP, GVP, GDP, GTP, GPP, GACP)
- Quality Management Systems (QMS) implementation
- ALCOA+ data integrity framework