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Stratergic Sourcing

We offer new molecules & their intermediates with along with proper documentation required for regulatory Filling from renowned plants across the globe.

Extended support on Regulatory documentation for registration purpose with technical expertise in GMP & GDUFA.

Our effective outsourcing solutions are the hallmark of our business which have been offering to our precious customers, right from obtaining the amount of wholesale and retail pharmaceutical API’s.

Strategic Sourcing - Raw material sourcing globally based on Customers specification.

Serving major pharmaceutical companies to R&D facilities, small facilities to remotely placed facilities and institutions– efficiently and promptly across the globe.

Process development - Ability to arrange supply of products with non infringing routes and can work with your process, or arrange to develop a new process; process development to simplify and improve difficult or expensive synthetic routes in very many cases.

Registration

We are partnering with our overseas manufacturers for the registration of their pharmaceuticals products with the Indian Drug Regulatory Authority

For any further clarification, you may kindly requested to write to us or call upon us and we would be pleased to answer all your queries.

On site Audit

An on-site GMP audit will identify any GMP non-compliance (gap analysis) and recommend how they should be addressed. This is by far the best way to ensure that a company is GMP compliant and regulatory audit ready.

  • We facilitate GMP auditing for equipment, facilities, utilities, processes and process installations.

  • We facilitate onsite factory audits to assure that pharmaceutical intermediates are produced consistently and are strictly controlled to meet both national and international standards appropriate for their intended use. We assist our sources to ensure that related -regulatory requirements (FDA) are met.
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