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Over the years, from representing local businesses in the Pharmaceutical Industry, we have grown to represent manufacturers and distributors globally; and in the process, developed a network so comprehensive that it defines who we are and how we work as well.
Aastrid offers a range of services for acquiring regulatory approvals/ product registrations. For APIs and excipients, we provide comprehensive services for preparing European Drug Master Files, as well as preparing, submitting, and following up with EDQM Certification of Suitability applications