At SG we can help the customer minimize their risks by adding our site as a secondary site which can be done by transferring an existing MA to SG and adding SG as an additional site. We have a team of 15 scientists in the technology transfer team and 8 project managers who can help the customer site transfer an existing Market authorization in to steril-gene.
We work with the customer to get all the technical documents from the MA and do feasibility trials in RnD facility. Once the trials are successful, our team then transfers the product to GMP area and completes Scale up, process optimization and exhibit batches which then gets loaded on to stability.
We have a dedicated documentation team who them transfers the completed documents to the customer who then compiles the dossier and submits it to the regulatory authorities.
Click here to reach out to us for a Site Transfer project requirement