About Sushen Medicamentos Private Limited Ahmedabad:
SUSHEN Medicamentos Pvt. Ltd. (SUSHEN), is a global company of end-to-end pharmaceutical services with focus on drug delivery research and product development. SUSHEN’s expertise and flexibility can bring a complex formulation project in to clinical and bioequivalence withsuperior quality, innovative solution. At SUSHEN, we provide complete turnkey solutions to the pharmaceutical industry, right from conceptualizing and designing a new plant to its construction and setting up of manufacturing facilities to its commissioning.
Whether your goal is to improve bio-availability, achieve bio-equivalence, or develop a new product, SUSHEN’s innovative approach to Formulation Development will meet your expectations.
Over the years, we have acquired global expertise in coordinating and implementing Greenfield projects, which benefit our clients through timely and economical completion of their projects.
SUSHEN exploits its broad experience in pharmaceutical product development as well as its modern research facility to offer contract development services for our clients.
We decided to further advance its reach and scope by developing quality and value added generic Drug Product forms in the oral solid dosageform. Today, SUSHEN proudly offers several worldwide dossiers.
We are a CDMO committed to helping you take your products from early development through to commercial manufacturing.
We’ve been around for a while and we’re proud of the company we’ve built which is why we want you to know we are here for you today and we’ll be here for you tomorrow too. That’s the SUSHEN way.
There are lots of CDMOs in the world. But none quite like SUSHEN despite the scale and size of our company, we conduct our business in the right way, by respecting all stakeholders at all times and delivering value for money to our clients.
Our development & technology division offers clients a comprehensive range of services, with the aim of supporting the customer from the initial product concept to the approved pharmaceutical drug, in some cases, through various forms of risk sharing.
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