✓ USFDA Approved ✓ EDQM Approved ✓ TOWA Japan Inspected ✓ ISO 9001:2015 Certified

Welcome to Gensynth Labs

Gensynth Laboratories Pvt. Ltd. is a USFDA and EDQM approved manufacturer of Advanced Pharmaceutical Intermediates and API Key Starting Materials. Strategically located in Pashamylaram, Hyderabad, our robust manufacturing infrastructure is aggressively engaged in expanding its product portfolio. Our fully equipped R&D center provides us with a sustainable competitive advantage to deliver cost-effective, high-quality products to the global pharmaceutical market.

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Our Core Capabilities

Process Development

Developing novel processes for complex intermediates with a focus on yield optimization and environmental safety.

Scale-Up & Tech Transfer

Seamlessly scaling up highly diversified reactions from R&D bench to commercial manufacturing levels.

Quality Assurance

Stringent QMS covering Change Controls, Deviations, and strict adherence to global CGMP standards.

Featured Commercial Products

We manufacture critical intermediates for high-value APIs.

API Category Key Intermediate CAS Number
Atorvastatin Atorvastatin acetonide tert-butyl ester 125971-95-1
Posaconazole N'-((2S.3S)-2-(Benzyloxy)pentan-3-yl)formohydrazide oxalate 1887197-42-3
Ziprasidone 3-(1-Piperazinyl)-1,2-benzisothiazole 87691-87-0
Candesartan Methyl-1-[(2-cyanobiphenyl-4-yl)methyl]-2-ethoxybenzimidazole-7-carboxylate 139481-44-0

Robust Manufacturing Infrastructure

Operating 45 Reactors (SSR/GLR) with specialized capabilities in cryogenic reactions up to -78°C and high-temp reactions up to 200°C.