Pharmaceutical Manufacturing & Export Solutions

Built on Trust, Compliance & Commercial Consistency

At Cross Corporation, our business model is structured to meet the demanding expectations of both regulated and semi-regulated international markets. Overseas partners work directly with a technically competent Indian manufacturer and reliable supplier on a regular basis.

We specialize in product-specific development and R&D-driven manufacturing, tailoring formulations to meet country-specific regulatory, climatic (Zone IVb), and market requirements. Furthermore, we actively monitor upcoming patent expiries to develop timely generic versions that enable rapid market entry immediately upon patent expiration.

From Registration Batches to Multi-Year Scalable Supply

Every project is approached with a long-term vision — from trial registration batches, stability testing, and MOH submissions to repeat export shipments over multi-year registration validity cycles.

• Direct technical engagement with formulation chemists
• State-of-the-art manufacturing across Gujarat & Himachal
• Full dossier preparation: COPP, MOA, COA & Stability

FDF Formulation & Manufacturing

Commercial manufacturing of solid, liquid, and semi-solid dosage forms under USFDA, EUGMP, GCC, and WHO-GMP compliant environments.

Controlled Drugs & NDPS Compliance

Specialized expertise in handling prescription medicines, controlled substances, CDSCO export NOCs, State FDCA permissions, and NDPS Act compliance.

Patent-Expiry Generic Formulations

Proactive patent tracking allows us to formulate and validate robust generic equivalents ahead of time, empowering overseas partners to achieve rapid first-to-market advantage upon expiry.

Repeat International Commercial Supply

We structure long-term commercial relationships centered around authorized product registrations, ensuring predictable lead times, batch consistency, and stable pricing over multi-year periods.