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A New Prescription for Regulatory Compliance:Syntel’s Intelligent Regulatory Services Platform

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Global life sciences companies are facing exceptional business pressure. In today’s evolving regulatory environment, new directives and regulations increasingly pose not just a long term need, but a real-time operational challenge as well.

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Syntel’s Prescription for Automating Pharmacovigilance Adverse Events Management

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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).

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

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Life Sciences companies face many challenges delivering product labels tailored to every global market where they compete. Successful labeling requires compliance with a diverse set of ever-changing global and local regulatory standards, country-specific translations, and strict attention to compliance and consistency throughout the value chain.

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Increasing Accuracy and Efficiency by Automating Label Proofing and Quality Control

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The client is a leading medical devices company specializing in sterilization products sold across the globe. In order to bring their products to market faster and reduce errors, they needed to automate the proofing and quality control process for their multilingual labels.

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http://www.syntelinc.com/sites/default/files/success_stories_pdf/SYNT_Life_Sciences_Labeling_Automation_Case_Study.pdf

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Reducing Pharma Regulatory Submission Turnaround Time by 20%

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The client is a top-10 global pharmaceutical company. They wanted to quickly register their existing products in new markets such as Europe, Canada, and the U.S. They needed a scalable and flexible operating model along with a team with expertise in global regulatory requirements. They chose Syntel as their partner, based on our expertise and ability to meet their stringent deadlines.

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http://www.syntelinc.com/sites/default/files/success_stories_pdf/SYNT_Life_Sciences_Regulatory_Case_Study.pdf

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Implementing Dynamic Packaging Engineering for a Global Medical Device Manufacturer

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The client is a global leader in spinal implants, with R&D facilities in the U.S. and manufacturing in Europe. They offer more than 10,000 separate products, including cages, rods, hooks, connectors, plates and screws. They turned to Syntel for help creating a more responsive, dynamic process for managing packaging designs for this wide array of products.

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Syntel to Announce Second Quarter 2017 Results on Thursday, July 20, 2017

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Friday, July 14, 2017

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Syntel Names Rakesh Khanna CEO and President

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Tuesday, July 18, 2017

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Syntel Reports Second Quarter 2017 Financial Results

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Thursday, July 20, 2017

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SAP HANA

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Overview

Complex business environment and technological advancements pose new challenges to traditional IT that include democratization of data, cost optimization, and insights to make faster decisions. Business success depends on response to change in customer, market, and competition. It requires faster consumption of data and insight-driven decision making. Syntel pursues SAP HANA as not just a next-generation in-memory computing database, but also enables to respond quickly for fast changing business requirements.

Success Stories

50% Faster Financial Period Cycles by...

50% Faster Financial Period Cycles by Implementing SAP HANA

A large personal line insurer wanted to consolidate BW systems to a Digital Enterprise Platform to improve efficiency, and reduce maintenance cost, complexity, and data redundancy. With ever increasing data volumes, they needed a robust framework to help them derive information from data for taking key business decisions.

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Fortune 100 Insurer Transforms From SAP BW to...

Fortune 100 Insurer Transforms From SAP BW to SAP HANA

The client is a Fortune 100 insurance company that was looking to replace an aging SAP Business Warehouse (BW) system with a high degree of data redundancy to the more modern, in-memory SAP HANA platform.

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Increasing Market Share And Reducing Cost With...

Increasing Market Share And Reducing Cost With SAP HANA Analytics

The client is a leading U.S. automaker that was looking to increase their market share to 40% and reduce costs by 10%. They determined that implementing an SAP HANA data mart and applying analytics to inform their decision making for sales, warranty, and extended warranty was one of the keys to achieving this goal.

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Key Offerings

Our SAP HANA offerings help businesses take advantage of digital core and become more agile.

S/4 HANA

Migrate or implement S/4 HANA so that processes and analysis can be done on a single platform

Advanced analytics powered by HANA

Derive actionable insights using HANA platform and predictive analytics

 

SAP Business Warehouse (BW) on HANA

Migrate to BW/4 HANA from SAP BW and reduce total cost of ownership

Accelerated HANA migration

Optimize ECC migration to HANA

Digital Experience

Improve employee productivity by deploying Fiori apps

Key Benefits

30% Reduction in project lifecycle – Faster time to market

20% boost in business process efficiency

Revenue growth through HANA Predictive analytics

Automated testing which drastically reduce the efforts

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Let Syntel make your Business Smarter with SAP HANA Analytics

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Today’s complex business environment demands real-time insights and powerful reporting capabilities in order to adapt to changing market conditions and evolving customer demands. Unparalleled business insight exists in the unprecedented amount of data available today, but you need the right analytics tool to take advantage of it. SAP HANA is a next generation in-memory computing database with the speed and power to meet the demands of the Digital Age.

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Power your Digital Transformation with Transform One from Syntel

Syntel's Life Sciences Solutions

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With Syntel Since

with Syntel Since 1993

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Evolve The Core with Syntel’s Product Engineering Services Powered by Automation

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With more and more organizations scrambling to modernize their operations for the digital age, speed and quality have become the two most vital elements to ensure a rich user experience and seamless service delivery.

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Syntel helps Automate UK Based Multinational General Insurance Company’s Contact Center Operations

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A UK based multinational general insurance company was looking to reduce its operational expenditure and deliver improved customer experience through process automation. Their customer contact center operations constituted multiple application touch points and completing any single process (like policy enquiry, cancellation, premium payment, policy servicing etc.) required switching between a minimum of 3 to 4 applications, copy-pasting information from one application to another. Training costs for customer managers were high and improved MIS reporting and decision making was the need of the hour.

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Syntel Automates IT Ops for Faster Ticket Resolution for A Leading Credit Rating Agency

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Our client is a leading credit rating agency, wanted to automate their ticketing system in a bid to eliminate errors introduced due to human intervention, thereby improving productivity and reducing the turnaround time for ticket resolution.

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Regulatory Submission Publishing

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A Trusted, Experienced Partner for Regulatory Submissions

The number of clinical documents required by regulatory agencies has increased dramatically with new drug and device safety guidelines. Syntel can help you meet these dynamic regulatory requirements with a suite of submission publishing services for all phases of the pharmaceutical and medical device development process, including consulting, compilation and submission lifecycle management, as well as regulatory IT services.

Our publishing team is made up of doctors, life sciences experts, and technology specialists ready to translate your complex data and results into formatted, regulatory-compliant documents — enabling you to meet strict timelines and secure approvals for your products across multiple global markets.

Pharmaceuticals and biotech
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Offerings

Regulatory Consulting Services

  • Regional regulatory consulting
  • Strategic planning for fast-tracked products
  • Global regulatory intelligence 
  • Gap analysis

Pre-Approval Services

  • Dossier compilation services for FDA, EU, Canada, LATAM, APAC & ROW countries
  • Dossier compilation and publishing common technical documents (CTD), eCTD, and non-eCTD electronic submission (NeeS) modules for US, EU, Canada & APAC
  • Drug Master Files (DMFs)

Post-Approval Services

  • Lifecycle support for variations, renewals and annual reports
  • License renewal for Rest of World (ROW) countries
  • Regulatory affairs strategic guidance

Submission Services

  • End-to end submission publishing services, including document formatting, publishing and quality control

The Syntel Advantage

  • Expert team to meet regional regulatory requirements for US Federal Drug Administration (FDA), European Union (EU), Latin American (LATAM), Asia Pacific (APAC) & Rest of World (ROW)
  • Consolidated framework for end-to-enddocument management & processing capabilities, including dossier preparation, quality control, submission review and filing
  • Intelligent process automation tools to support accelerated processing and operational enhancements
  • Scalable, flexible global team to optimize costs and manage peaks and valleys in your submission schedule
  • Strategic commitment to invest in solutions, competencies, IP, and infrastructure for regulatory services
  • Agile methodology to quickly implement revised plans as regulatory requirements change

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Syntel to Announce Third Quarter 2017 Results on Tuesday, October 17, 2017

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Thursday, October 12, 2017

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Syntel Reports Third Quarter 2017 Financial Results

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Tuesday, October 17, 2017

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