Aetos Pharma can provide its clients the customized manufacturing as per the client’s need with their brand name, attractive packaging, and quality material needed keeping in mind the respective regulatory requirements of the country.
Our team at Aetos Pharma helps our international clients in dossier filling as per their regulatory requirements of respective countries in CTD, ACTD, and eCTD formats.
We help in the complete process starting from dossier preparation, dossier submission, and queries in dossiers from respective ministries of health to our international clients in various countries globally.
We also provide the COA (certificate of analysis), MOA (method of analysis), FSC (free sale certificate), COPP / CPP ( certificate of pharmaceutical product), PP ( product permission), etc all the documents required for the import license/import permit to our clients.
Aetos Pharma can provide technology transfer starting from API sourcing, equipment/machinery procurement, and formulation of finished dosage form from lab scale to commercial development and packaging.