Here at Saneca Pharma, our expert team of regulatory experts are committed to managing the complexities of your development and transfer projects.
Our experience working with authorities across Europe ensures your regulatory documentation is compiled accurately and efficiently, allowing you to send submissions to authorities earlier and speeding up your products’ time to market.
Our team has produced many electronic common technical document (eCTD) format dossiers and variations,allowing Saneca Pharma to produce variations for customers to submit when they transfers to our site in Hlohovec, Slovakia.
If you are looking for a CDMO partner to support your product development requirements, our regulatory team has the skills and expertise to submit more detailed documents.
For more information on our regulatory services, contact us.
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