Zen Consultech has conceptualized and engineered advanced facilities across API, High Potent API (HPAI), peptides, and sterile API segments for leading pharmaceutical companies. Our designs adhere to the highest global standards, including NBC, Factory Acts, ISPE Baseline Guides, ICH Q7 & Q9, FDA, WHO, OSHA, and NFPA.

Our engineering teams are proficient in designing containment strategies and closed-transfer systems tailored to the potency classification and handling requirements of each product.

Our experience spans complex and hazardous chemistries such as hydrogenation, cryogenic reactions, sodium metal handling, nitration, bromination, and various other specialized processes.

Our deep database, sector insights, and in-house expertise make Zen one of the most trusted engineering partners in the pharmaceutical domain.

Pharma Segments We Serve Active Pharmaceutical Ingredients (API), High Potent APIs (HPAI), Sterile, Aseptic & Non-Sterile Manufacturing, Hormones, Steroids & Oncology, Pilot Plants & Scale-Up. Facilities

Our capabilities span all dosage forms—oral solids, injectables, liquids, creams, ointments, aerosols, oncology formulations, diagnostics, and medical devices.

We deliver fully compliant facilities aligned with ISPE, USFDA, EU-GMP, and other global standards.

Zen Consultech offers end-to-end solutions across raw material handling, processing, filling, packaging, and storage.

Benefits to Client:

Dr. Reddy’s CTO-SEZ, ONCO ASD, Pydibhimavaram – Dedicated Oncology (ONCO ASD, OEB-05) facility featuring spray drying systems, 40 KL total reactor capacity, 8 isolators, and 3 modular cleanroom suites, engineered for high-containment and regulatory compliance. Scope includes Gap assessment in basic engineering, Detail engineering for the production block, 3D modelling & Containment systems planning.