API & Bulk Drugs

Strategix Asia provides expert Consulting and Engineering services for Active Pharmaceutical Ingredient (API) and bulk drug manufacturing
facilities, focusing on safety, regulatory adherence, and process efficiency.

Our designs are compliant with cGMP, US FDA, EMA, and other regulatory standards, incorporating critical engineering elements such as containment for potent compounds, solvent recovery systems, waste management, and hazardous area classification.

We guide clients through every phase process design, Equipment Engineering, Facility Layout, Qualification, and Validation To Establish
Scalable, High quality production environments for APIs and intermediates.

Our portfolio includes successful execution of the following facility types:

Multi-Product and Dedicated API Plant Design

Environmental Health and Safety (EHS) Integration

Solvent Storage, Handling, and Recovery Systems

High Potency and Cytotoxic Compound Manufacturing Facilities

Waste Treatment and Effluent Management

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