Consultancy & Executive Interim Management
MedTech and Pharma
Sourcimedics BV supports MedTech and Pharma organizations with experienced interim leadership, senior consulting, and targeted training during periods of growth, transformation, and complex business challenges.
I am Piet Bron, owner of Sourcimedics, with more than 25 years of international leadership and hands-on experience helping companies navigate critical challenges across Quality Management, Product Design & Development, Regulatory Affairs, Risk Management, Global Vigilance, and Compliance
Through Sourcimedics, I provide practical leadership and support in areas including QMS improvement and integration, audit readiness and follow-up, compliance remediation, product development and regulatory approvals, responses to regulatory inquiries, and organizational change.
When broader expertise or additional capacity is required, Sourcimedics can draw on a trusted network of experienced professionals and collaborate with selected partner firms. This keeps assignments flexible and practical while bringing in the right expertise for the challenge at hand.
My focus is to create clarity, strengthen quality culture, improve regulatory readiness, and help organizations deliver safe, reliable products with confidence.
Expertise & Services
Quality Management & Compliance
Driving quality excellence by strengthening governance, processes, and Quality Management Systems, improving regulatory compliance, and achieving inspection readiness through effective audits, remediation programs, and QMS integration activities
Product Design & Development
Providing senior direction and hands-on execution for complex product development initiatives, from concept through design transfer. Strengthening design controls, risk management, verification and validation, and regulatory readiness to enable the succesful launch of safe, effective, and compliant products.
Risk Management & global Vigilance
Providing direction and hands-on execution for risk management and global vigilance activities, strengthening post-market surveillance, complaint handling, signal management, adverse event reporting, and regulatory compliance to support safe and compliant products.
Regulatory Affairs
Providing strategic leadership throughout the product lifecycle, from regulatory strategy and submissions to technical documentation, change management, and market access. Translating complex global regulatory requirements into practical pathways that support timely approvals, sustained compliance, and successful commercialization.
Executive Interim Management
Providing experienced interim leadership for MedTech and Pharmaceutical organizations during periods of transition, growth, transformation, or increased operational pressure. Taking hands-on responsibility for teams, priorities, and critical programs while creating structure, strengthening execution, aligning stakeholders, and delivering sustainable results.
Organizational Development & Training
Building lean, compliant, and high-performing organizations through leadership development, targeted training, and practical coaching. Strengthening clear roles and responsibilities, effective governance, efficient processes, and a strong quality and compliance culture that drives sustainable performance.