Manage My Transfer
What You Are Dealing With
You are executing a technology transfer and the margin for error is narrow. A product that cannot be consistently reproduced at the receiving site means delays, revalidation costs, and potential supply disruption. These projects are technically complex, often multi-year, and require tight coordination between sending and receiving sites, CMOs, and regulatory teams simultaneously. The knowledge gaps that cause transfers to fail are rarely obvious at the start. They surface midway through, when they are most expensive to address.
How We Approach It
We provide senior project management and technical oversight across the full transfer lifecycle. That includes gap analysis, quality planning, validation master plan support, process validation, equipment qualification, cleaning validation, and schedule and resource management from planning through commercial ramp-up. We work onsite when it matters and manage the documentation and regulatory requirements that make or break the transfer.
What We Have Done
A pharmaceutical company completing Phase III clinical trials engaged MEDVACON to support commercialization of their product. MEDVACON provided full compliance support across process validation, equipment qualification, cleaning validation, technology transfer, and laboratory instrument qualification for both the client and their CMO.
A market leader in transdermal therapeutic systems engaged MEDVACON to support the technical transfer of their treatment for Parkinson’s disease and restless leg syndrome into their New Jersey manufacturing site. MEDVACON analyzed transfer data and acceptance criteria to ensure a compliant and successful transfer.