Success Stories

Learn more about the value and business results we create for our clients every day.

Digital Services

Helping a Top Global Medical Device and Pharmaceutical Company Comply with the EU Regulations

The regulations companies have to comply with are increasing and could pose temporary challenges for businesses. Assessing the impact of the regulations on business is therefore important as altered policies may require the organizations to change in the way they do business.

Upgrading the Ophthalmic Product Manufacturer’s Quality Management Systems for EU MDR

The global regulatory environment is going through a continuous change with regulations governing significant businesses are regularly altered. Companies are at risk of losing the majority of their business if they do not comply with the changed regulations.

Implementing Dynamic Packaging Engineering for a Global Medical Device Manufacturer

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 us for help.

Reducing Pharma Regulatory Submission Turnaround Time by 20%

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 chose Atos Syntel as their partner, based on our expertise and ability to meet their stringent deadlines.

Increasing Accuracy and Efficiency by Automating Label Proofing and Quality Control

The client is a leading medical devices company specializing in sterilization products. See how Atos Syntel enabled them to bring their products to market faster and reduce errors with automated proofing and quality control for their multilingual labels.

Reducing Label Data Migration Turnaround Time by 35% for a Medical Device Company

The client is a top global medical device company and a worldwide leader in home medical equipment. They were facing issues with data standardization, data duplication and data loss, since past data migrations had been handled manually

Helping a Client Meet 21CFR11 Regulations and Guidelines

The client is a global medical device, pharmaceutical and biotech company. They were facing increased litigation due to regulatory submissions that did not adhere with FDA 21CFR11 regulations. They needed help ensuring their applications were compliant in GxP regulated areas.

Managed Services Model Helps Save 60% on Label Design, Artwork Management and Proofing

The client is a top global medical device company and a worldwide leader in cardiology and endovascular devices. To keep up with the latest trends, they planned to change their label design and artwork. They turned to Atos Syntel for an impact analysis before migrating

Implementing GS1/UDI Compliant Labels for a Medical Device Company

The client is an American manufacturer of surgical instruments. They wanted to adopt GS1/UDI standards, a system used to assign Unique Device Identification (UDI) numbers to medical devices. UDI compliance is a requirement for any medical device manufacturer

Leveraging Business Rules Extraction To Eliminate Modernization Risk

Our client is a leading North American insurer, wanted to eliminate performance bottlenecks caused by legacy applications, so they set out to modernize business-critical core systems by migrating to new platforms that would enable new technologies to be integrated.