Publications

Read more about the thinking that enables Syntel to deliver value to our clients.

Digital Services

Transform Labeling and Packaging with Next-Generation Automated Services from Syntel

Life Sciences companies face many challenges delivering product labels tailored to every global market where they compete.

Syntel’s Prescription for Automating Pharmacovigilance Adverse Events Management

It’s no secret that drug and device safety is of the utmost importance in today’s competitive life sciences marketplace, and pharmacovigilance (PV) is a major component of an effective drug regulation system for evaluating and monitoring adverse events (AEs).

Evolving to Next Generation Clinical Data Management Services

With 40% of drugs going off patent in the near future, increasing demand for accessible healthcare and a patient-centric approach, and pressure on the payer sector, the life sciences industry today demands innovation and excellence in order to succeed.

Optimize Performance by Harmonizing Computer System Validation

Computer system validation (CSV) is an integral process for pharmaceutical, biotech and medical device companies.

Centralized Global Partner to Support Scalable Model for Future Generation e-DMS

Dealing with multiple Document Management Systems (DMS) across multiple teams around the globe is a challenge for the Pharmaceutical industry. In order to realize tangible benefits from

Operational Model for Pharmacovigilance

Global Health Regulatory Agencies mandate all Pharmaceutical and Modern Drug Discovery companies to collect, process, and report adverse events. Organizations failing to achieve 100% compliance may face penalties or face drug withdrawal from the market.

Syntel’s Trial Master File Management

It is imperative and crucial for organizations to produce requested clinical records on time for various inspections and audits. Life sciences, medical devices and contract research organizations find it difficult and time consuming to cater such requirements.

Implementing a Scalable eTMF Model for Faster Clinical Trials and Drug Launches

Clinical records need to be produced in a timely manner for inspections and audits, but for many life sciences, medical devices, and research organizations, meeting such requirements is a difficult and time consuming task. Due to the collaborative nature of producing requ

Syntel’s Smart Pharma Solution - Improving Quality of Life for Patients

In today’s world, digital innovation in life sciences predominantly focuses on consumers and external collaboration, not on end-user empowerment.