- Banking and Financial Services
- Life Sciences
- Logistics and Travel
- Core Services
- Product Engineering
- Continuous Testing
- Enterprise Solutions
- IT Ops
- Legacy Modernization
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).
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.
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.
Computer system validation (CSV) is an integral process for pharmaceutical, biotech and medical device companies.
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
The Life Sciences industry has entered a new era with increasing competitive pressures, a rapidly evolving healthcare landscape, disruptive digital technology changes, and deeper regulatory scrutiny.