Since our inception, we have put utmost importance towards quality while taking into consideration the user requirements and their needs. We focus on the ongoing and upcoming industry and regulatory trends and do our best to incorporate them to build state of the art facilities.
The fundamental block of any Project. Providing GMP compliant systems taking into consideration GEP and business requirements.
Providing and executing an efficient workflow with a smooth timeline. While working harmoniously with other contractors and consultants.
Validation is the heart and soul of any pharmaceutical project. And we believe in implementing accurate validation and commissioning processes with special focus on the documentation practices. While staying up to date with the current industrial norms, regulatory, and cGMP practices.
Our Services are not bound by the borders. And we strongly believe in expanding our horizons to the best possible scenarios. Currently, we have executed projects in more than 10 countries worldwide, Mostly in the Asian subcontinent, Africa, CIS countires, and so on. However, we constantly aspire to increase our global footprint.
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