Pharmaceuticals

We manufacture a comprehensive range of pharmaceutical formulations — tablets, capsules, injectables, infusions, inhalers, and more — fully compliant with US FDA, EU GMP, and WHO-cGMP standards.

Nutraceuticals

We are a certified nutraceutical manufacturer accredited by Health Canada and US FDA, producing premium nutritional supplements, herbal, and ayurvedic products to the highest international standards.

Veterinary Pharmaceuticals

We develop and supply high-quality veterinary pharmaceutical and nutraceutical products designed to improve animal health across companion animals, livestock, poultry, equine, and aquaculture.

Regulatory Affairs Support

Our experienced in-house regulatory team delivers timely, high-quality dossier submissions in CTD, eCTD, and ACTD formats, supporting product registration across 30+ countries worldwide.

Contract Manufacturing (CMO/CDMO)

We offer comprehensive CMO and CDMO services — from formulation development and clinical trials to full-scale GMP-compliant commercial production — customized to your product and market.

Research & Development

Our R&D team combines scientific expertise with advanced formulation technologies to develop affordable, high-quality pharmaceutical and nutraceutical solutions responding to evolving healthcare needs.


Service Excellence

Quality at Every Step

Internationally Certified Quality Standards

Our Quality Management team works to ensure that every product consistently meets internationally accepted standards of purity, safety, and performance. Supported by a strong Quality Assurance framework, we implement the latest ICH guidelines, maintain robust Good Manufacturing Practices (GMPs), Good Laboratory Practices and Standard Operating Procedures (SOPs) and conduct regular internal and external audits to ensure continuous compliance.

200+ Dossiers Filed
30+ Countries Served
500+ Products

What We Do

A one-stop destination for global healthcare solutions

We are a one-stop destination for pharmaceutical formulation development, clinical trials, bioequivalence studies, and contract manufacturing. At the heart of everything we do is a relentless drive to innovate. We are committed to pharmaceutical research and development, identifying and advancing next-generation therapeutic solutions. Our in-house Regulatory Affairs team is made up of professionals with strong expertise in global regulatory frameworks and compliance requirements.

Regulatory Compliance
90%

30+

Countries Served

500+

Products in Portfolio

Shivahi Exim

Global Pharma Partner


At a Glance

Why Partner with Shivahi Exim

We bring efficiency, expertise, and commitment to every partnership. By combining deep market knowledge, a strong established customer base, and proven ground-level operations, we help our partners reduce risks, lower fixed costs, and expand their product reach globally.

Deep market knowledge and an established global customer network across four continents
Ready Dossiers and documents for seamless market entry
Flexible, customized solutions for both suppliers and customers
Specialized capability in specialty molecule manufacturing, Technology Transfer, and Co-Development
Rapid generic drug development backed by reliable contract research services
Consistent, internationally compliant quality across all products and markets