Take Solutions Ltd, the Chennai-based technology company focusing on life sciences (LS) sector, entered into definitive agreements on November 18, 2015 to acquire Ecron Acunova (EA), a life sciences services player, for Rs 115 crores.
The acquisition will enable Take to add expertise in the areas of biosimilars, regenerative medicine and diagnostic imaging agents segments which are emerging growth areas. This will help Take Solutions to move into the addressable market for its services to $ 30 billion. It will also significantly enhance presence in Europe and Nordic countries.
“Globally, there is a growing focus on quality, data, analytics and outcomes in the industry, resulting in increased pharma/biotech R&D spending and funding. This acquisition will enhance our addressable market from $ 15.9 billion to over $ 30 billion by 2019, giving us great headroom for growth,” opined Srinivasan H R, vice chairman & managing director, Take Solutions.
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With the acquisition of Ecron Acunova, Take will add audit ready infrastructure in Europe and India, and parts of South Asia to its expanding footprint. The organisation will also augment its pool of subject matter experts by 30 percent and life sciences talent by 50 percent, significantly amplifying its experience, innovation and domain expertise. In addition, the full service capability along with expanded infrastructure will allow Take Solutions to service the mid-market as well.
“Take & Ecron Acunova’s combined attributes will strengthen our position as a fully integrated differentiated life sciences services provider to large and small global pharmaceutical companies and thereby broaden the addressable market,” added Srinivasan.
Ecron Acunova is a life sciences services company delivering pharmaceutical research services to global clients across South East Asia, Central & Nordic Europe and North America. Along with catering to big pharma clients, EA’s capabilities lay in delivering highly specialised services to small/medium size biotech and pharma companies in the areas of pharmacovigilance, regulatory affairs, strategic consulting, clinical data management and biostatistics, medical writing, clinical trials phases II-IV and bioavailability & bioequivalence (BA/BE).