Life Sciences Software Development Services

Aces up our sleeves:

• Know-how in the Life Science industry – 10+ projects implemented for customers from the life-sciences industry. Successful collaboration with clients such as drug producers, hospitals, biotechnology, healthcare, medical equipment producers
• GAMP Best Practices compliance – which guarantees the highest quality and safety of implemented software
• Experts on board – IT system validation for Life Sciences companies specialists
• 15 years of international market experience – for example, in Germany or Poland
• Best security measures in our company – proven by the ISO 27001 certificate

The signpost for Quality Assurance and IT departments in pharmaceutical companies is “GAMP®5 Concept of Compliance of Computerized Systems with GxP Based on Risk Management“. This guide defines the best practices for ensuring compliance with GxP (GMP, GDP, GCP) regulations in the field of implementation and operation of computerized and automated systems, providing guidelines for consulting companies and suppliers of computerized systems in the Life Sciences sector.

Safety & security of your systems and data

In order to minimize the risk of errors, various types of processes are implemented in pharmaceutical companies to re-check all dependencies and efficiency of mechanisms. These are, among others: functionality, process, data and authorization tests, user training and documentation, procedures, as well as the necessary reconstruction of functions.

Our trust in IT solutions grows in proportion to the technological development of systems, especially their reliability. They are becoming more and more effective, allowing to increase the pace of production and minimize mistakes. However, when human life is at stake, even the smallest details must not be forgotten. A computer program is made by a fallible man.

Therefore, it is worth providing tests, security and processes that will ensure that a defective drug will not be produced, and at the same time will ensure the possibility of its recall as soon as possible, if such a product does enter the market.

As you can see, people, programs, processes and procedures are standing on a pharmacy shelf behind each package of a medicine. It is difficult to break through errors through such safeguards. And scientists are constantly working to make it almost impossible.