Our Regulatory team consists of highly qualified personnel engaged in providing quality services in regulatory affairs documentation as per the Regulatory Guidelines of the different countries.
Our Regulatory Team can provide a complete support to register the Products.
Dossiers as per specific Guideline of all countries
Bio-Equivalence Studies with GLP certified clinical centers (BE Study)
Drug master Files (DMF)
Site Master File
Electronic Submission of Dossiers with all supporting documents
Certificate of Pharmaceutical Product (as per WHO), Free Sale Certificates, Certificate of Origin, Halal Certificates, Kosher Certificates, TSE-BSE Certificates.