Regulatory services:

SANA Pharma is capable for providing technical opinion concerning the registrability of products or companies through the review of the product dossiers, Drug Master Files, Site Master Files.
Also Sana Pharma is working to provide pharmaceutical companies with expert reports required for product registration such as clinical and non clinical study reports and also periodic safety update reports (PSUR).
Our qualified experts are ready to work as independent party for inspection of API’s or pharmaceutical manufacturing sites for regulatory purposes.