A WHO GMP ,ISO 9001-2008 and ISO 14000:2004 certified company, Shodhana Laboratories is considered to be one of the most dynamic Active Pharmaceutical Ingredients and Intermediates manufacturing companies. Our facility has been audited and approved by KFDA (Korea), COFEPRIS (Mexico) and TGA (Australia). Today, we have the technically most advanced production facilities and our entire manufacturing process is as per ICH & cGMP guidelines. We also have a world class R&D lab manned by a dynamic team of highly qualified and experienced scientists. Vision To become a respected company in the global pharmaceutical industry known for its technical capabilities, cGMP commitments and deliveries. Making our Mark. Incepted in the year 2000 by an enterprising technocrat (Doctorate in Chemistry) having more than three decades of industry experience with leading Indian pharmaceutical MNCs, Shodhana Laboratories Limited, today has steadily established itself as a fast-growing company with a wide range of APIs and intermediates Built On trust: At Shodhana, our product portfolio in bulk APIs and intermediates continues to add critical mass to our growth. Being at Hyderabad, it has an edge in terms of material sourcing, exporting, business networking, etc. Evolving through Research:  Shodhana has a well-equipped R&D center with strong and dynamic teams that are comprised of qualified and experienced scientists, who work round the clock on Process developments, New Product Development as well as Custom Chemical Synthesis.  It also holds a proven track record in developing products for the US, Europe and Australian markets.  It was even successful scaling up from lab process (milli gram) to pilot scale (several kilograms) to commercial scales (tons lots).  Besides successfully optimizing several processes in the lab, it also has the capabilities to develop novel/alternate processes.