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