SINCE 2007
SimSon Has Evolved. For a Healthier World.
SimSon Pharma Limited manufactures and supplies pharmaceutical reference standards, drug impurity standards, nitrosamine impurities, drug metabolites and stable isotope labelled compounds to pharmaceutical manufacturers, CROs and analytical laboratories worldwide.
SimSon was founded in 2007 in Mumbai and today runs four manufacturing and laboratory sites across India. Our work begins where the catalogue ends โ with the compound nobody has made, the peak nobody has identified and the standard a filing cannot proceed without.
To become a leading global pharmaceutical and scientific partner, recognized for solving complex chemistry challenges and enabling better outcomes.
To provide innovative, cost-effective and time-bound scientific solutions that help our customers move pharmaceutical research and development forward.
Select a stage to see what happens at it.
Synthesis, isolation and purification run in our own Indian laboratories, from milligrams for a method validation to bulk for a commercial programme.
Most suppliers ship what is already on a shelf. The requests that reach us are the ones that could not be answered anywhere else.
Unique impurities, hard-to-find molecules and complex standards with no published route and no commercial source โ designed and synthesised from first principles.
Identity, purity and assigned value established by NMR, mass spectrometry, IR, HPLC, GC, TGA/DSC and potency by mass balance โ every result in the certificate.
Traceable to recognised reference standards, with assigned value, uncertainty and supporting calculations. ISO 17034 for production, ISO/IEC 17025 for testing.
The same standard, the same documentation, whether you need five milligrams for a method or bulk supply for a commercial programme.
โWe started SimSon because the hardest requests in pharmaceutical chemistry were the ones nobody wanted to take.โ
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