The requirements of Life Sciences companies (including in the pharma and medical device space) inevitably change over time. Sometimes, a change is due to regulatory requirements; sometimes, customer needs change. Keep reading if you want to...

Implementing a Quality Management System is key to ensuring consistency in all your processes and, ultimately, guaranteeing your product quality and safety.  A well-established QMS will allow you to meet both customer and organizational requirements,...

No doubt the world has changed in recent years. Yet innovation in the medical field is stronger than ever. 

GMP stands for “good manufacturing practices.” Life Sciences companies need to be GMP-certified in order to produce and sell their products. But what do GMP guidelines entail? And how is GMP different from cGMP, or “current good manufacturing practic...

Companies in the Pharma and Medtech space need to cover all their bases before connecting with investors. The fundraising process may seem straightforward, but it’s important to understand how it might vary depending on your focus area and progress i...

Scilife has a new module! Finally, risk management is made a whole lot simpler, as well as accessible by everyone. In our webinar on Scilife's new Risk Assessment module, CEO Filip Heitbrink discusses:

Scilife adds a powerful Risk Assessment module to their digital Life Sciences platform. The latest in their broad repertoire of functional modules, Scilife adds Risk Assessment to the Scilife spectrum. This hotly awaited module, specifically designed...