Built like pharma. Engineered for scale.
A vertically integrated facility with in-house formulation R&D, ICH-compliant stability, and globally audited facilities – purpose-built to take ideas from molecule to market.
0 sq ft
Formulation R&D infrastructure
0 L
ICH-compliant stability storage
0+
Scientists across 5 functions
Infrastructure & Facilities
Formulation R&D Infrastructure
16,000 sq ft facility with a skilled scientific team.
Pilot Manufacturing
Seamless scale-up from lab to production batches.
Advanced Laboratories
Analytical, microbiology and stability testing units.
Granulation & Processing
Infrastructure for solid dosage development.
High-Capacity Stability Storage
1,38,000 L with ICH-compliant chambers.
End-to-End Setup
From formulation to finished-product readiness.
Dosage Form Capabilities
Oral Solids
Tablets (IR, SR, DR, CR), capsules, softgels.
Advanced Formats
Mouth-melts, ODT, effervescents, sachets, shots.
Liquid Orals
Drops, syrups, oral solutions.
Topical Systems
Gels, creams, emulgels.
Transdermal Delivery
Patches and sustained-release systems.
Multi-Format Integration
Single molecule across diverse delivery platforms.
Quality & Compliance
Regulatory Approvals
FSSAI and State FDA compliant facilities.
Analytical Excellence
HPLC, GC, UPLC, dissolution, wet lab testing.
Microbiological Control
Endotoxins, microbial limits, preservative efficacy.
Stability Validation
ICH-compliant long-term and accelerated studies.
Advanced Impurity Testing
Nitrosamines, elemental, genotoxic analysis.
Data Integrity Systems
Robust quality processes for global standards.
From molecule to market – across every format.
Formulation Development Suites
Tablet Manufacturing Suite
Twenty-one qualified systems – analytical to production.
Every instrument and machine on our floors is qualified, calibrated and SOP-driven for partner-grade reliability across development, manufacturing and quality control.
Analytical & Quality Control
- HPLC with UV, RI & PDA detector
- Gas Chromatography with Autosampler & Headspace
- UPLC with PDA
- Dissolution Tester
- UV-Visible Spectrophotometer
- FTIR Spectrophotometer
- Potentiometric Titrator
- Viscometer (RV & LV)
- Disintegration Tester
- Karl Fischer Titrator
- Melting Point Apparatus
Production & Processing
- Rapid Mixer Granulator
- Compression Machine
- Coating Machine
- Blender
- Capsule Filling Machine
- Liquid Filling Machine
- Sachet Filling Machine
- Rapid Dryer
- Fluid Bed Dryer (FBD)
- APCG – Top & Bottom Spray Granulation
- Homogenizer
People. Process. Products.
120+ team members including 40+ scientists across five vertically integrated functions – from ideation to regulatory – trusted by leading global pharma and nutraceutical partners.
- · End-to-end development engine from formulation to dossier submission and scale-up
- · Vertically integrated, global-compliant manufacturing infrastructure
- · Capacity to develop 10–15 products annually
A look inside our production floors.
Qualified, SOP-driven suites – from rapid-mixer granulation and compression to coating, blister and sachet packaging.
Audited & approved across seven global standards.
ISO/IEC 17025:2017 (NABL)
WHO Geneva – Audited & Approved
FSSAI Approved
CDSCO India
US FDA – Registered Facility
DSIR Registered
AYUSH Registered
Translate