End-to-end drug manufacturing services for pharmaceutical companies, distributors, and wholesale importers worldwide, compliant with international quality standards.
Full-scale production of branded and generic pharmaceuticals in all major dosage forms under cGMP conditions.
From concept to commercial production: new chemical entities, generic equivalents, and optimized formulations for better bioavailability.
Tablets (immediate/sustained release), capsules (hard/soft gel), injectables (ampoules/vials), syrups, ointments, suppositories, and sterile products.
Complete support for FDA, EMA, WHO-GMP, PIC/S, and other market approvals including dossier preparation and audit readiness.
Small batches, orphan drugs, controlled substances, and temperature-sensitive biologics with dedicated production lines.
Beyond manufacturing - complete solutions to streamline your pharmaceutical supply chain and market entry.
Blister packs (aluminum/PVC), bottles, sachets, vials with tamper-evident seals, and child-resistant options in compliance with destination country regulations.
White-label manufacturing with your branding, artwork, and package design without minimum order quantities for established products.
Full analytical testing (HPLC, GC, dissolution), microbiological analysis, stability studies (ICH guidelines), and batch release documentation.
Certificates of Analysis, GMP certificates, Certificate of Pharmaceutical Product (CPP), and all necessary export/import documentation.
Temperature-controlled storage (2-8°C, -20°C), validated shipping with data loggers, and INCOTERM solutions for global distribution.
End-to-end solutions including formulation development, drug production, packaging, quality testing, and regulatory support for global markets.
Yes, we specialize in small-batch production for niche medications, orphan drugs, and market testing with flexible minimum order quantities.
All major forms: tablets (IR/ER), capsules (hard/soft gel), injectables (vials/ampoules), syrups, creams, suppositories, and sterile products.
Our facilities include cold chain capabilities (2-8°C and -20°C storage) with validated shipping solutions for biologics and vaccines.
Our cGMP, EU-GMP, and WHO-GMP certified facilities have in-house QC labs performing HPLC, GC, dissolution testing, and microbial analysis.
Full analytical testing including HPLC, GC, dissolution, microbial limits, and stability studies following ICH guidelines.
Facilities are approved for cGMP, EU-GMP, WHO-GMP, and PIC/S with readiness for FDA, EMA, and other market inspections.
In our ICH-compliant stability chambers with real-time/accelerated studies, including climatic zone testing.
We produce established formulas under your brand name, handling everything from manufacturing to compliant packaging with your artwork.
No fixed minimums - we scale from pilot batches to commercial volumes based on your needs.
We supply all necessary documents: Certificates of Analysis, GMP certificates, CPP, and customized export paperwork.
Absolutely - we source specialty excipients including vegetarian capsules, gluten-free, and allergen-free components.
Our R&D team develops new formulations and improves existing ones for better bioavailability or patent circumvention.
Typically 6-12 months depending on formula complexity, with guidance from method validation to commercial production.
Blister packs (aluminum/PVC), bottles, sachets, vials with tamper-evident seals, and child-resistant options per destination requirements.
Yes, we maintain complete traceability and have protocols for market withdrawals with regulatory reporting assistance.