Who We Are
Farbridge Pharma Consulting is a leading expert in GxP Quality Assurance, distinguished by a proven record of excellence across Preclinical, Manufacturing, Distribution, Pharmacovigilance, and Clinical Trials.
Founded by a European Qualified Person in San Diego, California, and leveraging its global network, the Company is strategically positioned to serve as a bridge for biotech and pharmaceutical companies to establish, maintain and oversee activities in new countries, in compliance with applicable pharmaceutical regulations. It was founded with a singular vision: to harness our extensive expertise and specialized knowledge acquired over the years in GxP regulations globally. Through our team of multilingual local experts, we aim to facilitate seamless access for our clients to foreign clinical trials and markets.
Our Focus
At Farbridge Pharma Consulting, we specialize in delivering high-value consulting and training services to the life sciences industry. Our commitment to excellence extends to offering our services in multiple languages, ensuring effective communication and understanding across borders.
Our Expertise
Our core expertise spans the entire GxP spectrum, backed by a team of professionals with extensive local and international experience. We provide comprehensive Quality Assurance (QA) consulting and training services, along with tailored staffing solutions to meet the unique needs of our Clients.
Continuous Improvement
At Farbridge, we are unwavering in our dedication to continuous improvement. We believe in applying the principles of continuous improvement not only to our Clients’ systems but also to ourselves as consultants. Initiating clinical trials in another country can be challenging. However, we possess a track record of actively supporting companies as they expand into new markets. We gain invaluable experience that enriches our capabilities by working on diverse projects with a variety of teams and methodologies.
Collaborative Success
Farbridge Pharma Consulting operates as a cohesive consultancy team where no one stands alone. Our success is intertwined with the success of our clients. By recruiting top talent and providing them with exceptional training, we enable pharmaceutical and biotech companies to navigate the intricate landscape of GxP requirements with confidence. We are on your side and part of your team.
Investing in Our Team
We prioritize the growth and development of our team members by offering the resources and opportunities necessary for their personal and professional advancement. Our goal is to ensure that our internal and external Clients are not only satisfied but also poised for success.
Leveraging Experience
We harness the collective experience of our team members to deliver top-tier results, flexibility, and competent staffing solutions. Your success is our success, and we are committed to helping you achieve excellence in every endeavor.
Farbridge Pharma Consulting is your trusted partner in navigating the Quality Assurance and Compliance complexities of the life sciences industry. Attain compliance with International and Local Good Practices, regulations and quality guidelines through our expert team of GxP Quality Assurance consultants throughout the world who possess comprehensive expertise across the entire pharmaceutical GxP spectrum, including GMP, GCP, GVP, GLP, GDP, GTP, GPP and GACP.”
Our Services
We provide dedicated client support in the following key areas:
THE BRIDGE: ENSURING COMPLIANCE TO INTERNATIONAL QUALITY REQUIREMENTS
Initially focused on bridging the gap between North American and European quality requirements, we have extended our gap assessment services to other regions of the world (Central and South Americas, the United Kingdom, Switzerland, the Middle East, Africa and the Asia-Pacific region).
We first conduct a review of our Clients’ Quality Management Systems. Then, we adapt them to the new country-specific requirements. By doing so, we facilitate the expansion of their market exposure across continents while ensuring strict compliance with local quality regulations, thus fostering global growth opportunities.
GxP QUALITY SYSTEM BUILDING/UPGRADE
We are experts in Quality Management System (QMS) Implementation and Improvement, across all GxP.
We work in collaboration with your team and we follow a well-defined process:
- kick-off meeting with key stakeholders
- establish a list of necessary documents specific to your activities,
- build a plan to ensure their timely delivery,
- draft and review them, and
- ensure the whole project stays on track by meeting regularly with internal Subject Matter Experts.
GxP AUDITING
We have conducted countless audits around the world.
Our auditors have been carefully selected for their specialized knowledge in various regulations and technical fields. They are strategically positioned across key geographic regions, allowing us to serve you with your audit needs anywhere in the world,
- Quality Audits (Qualification, Routine and For Cause Audits)
- Due Diligence Audits (e.g., before Merge and Acquisition, on behalf of insurance companies, etc.)
- Mock Inspections (US FDA, EMA, MHRA, Swiss Medic, Health Canada, TGA, ANVISA, NMPA) by Senior Auditors or former Health Authorities Investigators/Inspectors
- European Qualified Person (QP) Audits
- Australian Authorized Person (AP) Audits
- Experience across all GxP, including audits of Service Providers (such as Contract Development and Manufacturing Organizations (CDMOs), Contract Research Organizations (CROs), Third-Party Logistics (TPLs), GCP Clinical Labs, GMP QC Labs, GLP In Vitro Testing Labs, Vivarium Labs, Pharmacovigilance Service Providers, Market Research Agencies, Regulatory Affairs Consulting firms, etc.), Clinical Sites, Suppliers, Blood Banks, GPP medicinal cannabis suppliers, GACP Medicinal plants suppliers, Commercial Partners, etc.
GxP TRAINING
We are committed to the professional development of our Clients and individual industry professionals. Our industry-specific training programs are designed to empower individuals and elevate their careers to new heights, equipping them with the latest knowledge, tools, and strategies necessary to thrive in the ever-changing pharmaceutical landscape, where staying ahead of any changes or advancement is paramount to success.
Visit our GxP Academy to discover our offering:
- Quality Assurance Training for Teams and Individuals (Good Practices, Regulations, Guidelines and Quality Tools)
- Hands on Auditor Training (through internal or external audits)
- Human-centric Training and Coaching (Leadership, Management and Quality Culture)
- Onsite, Live, and On-demand Courses
THE QA-CLINIC
Do you have a question? Our experts have the answer. With a network of more than 100 GxP consultants, there isn’t much we haven’t seen.
Fill out our contact form to get in touch. All questions are treated confidentially (covered by a non-disclosure agreement).
QA STAFFING AND RECRUITMENT
At Farbridge, we specialize in connecting top-tier Quality Assurance professionals with leading organizations in the life sciences sector. With deep industry expertise and a robust talent network, we understand the critical role that QA plays in ensuring product safety, regulatory compliance, and operational excellence.
We support Clients who need permanent, temporary or fractional seasoned Quality professionals, by recruiting candidates for our clients or by supplying onsite and remote consultants.
Join us on the journey to global success, where expertise meets opportunity. Should you require assistance with anything else, please do not hesitate to inform us here or send us an email at info@farbridgepharma.com
Our Mission
Bring tailored strategic and operational GxP Quality Assurance solutions to Life Sciences companies with expert multilingual quality consulting, auditing, training, staffing services, and in-depth experience in North American and European regulations.
Our Vision
To be the leading global partner for Quality Assurance consulting, supporting industry standards and best practices, as well as promoting compliance and continuous improvement to our partners.
Our Leadership
Stéphanie Verbrugghe, MPharm, QP, QPPV, the Founder and Chief Executive Officer of Farbridge Pharma Consulting, is a dynamic leader in the life sciences industry. With a distinguished global career, she brings a wealth of expertise as an Industrial Pharmacist and Quality Assurance Executive, fueled by her unwavering commitment to excellence and a deep passion for improving healthcare outcomes. Stéphanie’s extensive experience spans companies across Europe, Australia and North America covering cell and gene therapy products (ATMP/CGT) biotechnology, and pharmaceuticals. Her track record includes 8 Quality Management Systems and being a lead auditor for GMP and GVP. She holds coveted certifications, including Qualified Person (QP) and Qualified Person for Pharmacovigilance (QPPV) from the Belgian Health Authorities, and has been recognized as a Certified Pharmaceutical GMP Professional (CPGP) by ASQ, underlining her dedication to maintaining the highest quality standards. Stéphanie’s commitment to the life science industry extends beyond her role at Farbridge Pharma Consulting; she serves as a Board Member at Belwest, a Belgian-Luxembourg Chamber of Commerce serving thirteen western US states. With a master’s degree in Pharmaceutical Sciences and two additional ones in Industrial Pharmacy and Total Quality Management, Stephanie’s educational background complements her multifaceted leadership approach. She is known for her ability to inspire teams to achieve outstanding performance, fostering a culture of collaboration, excellence, and inclusivity.
Founder and CEO
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