- Banking and Financial Services
- Life Sciences
- Logistics and Travel
- Core Services
- Product Engineering
- Continuous Testing
- Enterprise Solutions
- IT Ops
- Legacy Modernization
Put Syntel’s efficient global model to work managing data and documentation, so you can bring new life saving therapies to market faster. Our services span the entire pharma and biotech value chain, from product development, clinical trials and regulatory approval, to packaging, marketing and managing customer feedback.
We also offer a comprehensive set of digital services to help transform your enterprise, connect with customers, and put the power of data to work for you.
Syntel enables future-ready life sciences companies to drive faster innovation, process excellence and compliance in an increasingly competitive and highly-regulated industry.
The client a German pharmaceutical company, and one of the largest API manufacturers in the world. They acquired a firm that largely operated on paper-based documentation, and asked Syntel to set-up a document management process to support the processing, archiving and retrieval of documents from the acquired company.download PDF
A large Japanese pharmaceutical company wanted to eliminate their dependence on paper-based Trial Master File (TMF) documentation, while standardizing processes and upgrading their technology environment.download PDF
The client, a top 10 global pharmaceutical company engaged Syntel to provide end-to-end Trial Master File (TMF) services. Later, as the document inventory increased, they began to face issues such as decentralized processes and a high level of inefficient manual work. They asked Syntel to explore how the TMF process could be automated through the SyntBots intelligent automation platform.download PDF