10 Small Submissions
No more than 10 Documents per submission
We are very well resourced with expert programmers, systems architects, data scientists and most important, specialists in our core domain, Regulatory Affairs across Life Sciences. Our strategy and design consultants will work with your team to understand your business processes, workflow and use cases. Only then, we will start formulating the best platforms to use as well as a likely set of solutions to pursue.
And just because an IT system is bespoke or leverages the latest in AI, Machine Learning and other automation, it does not mean that works in isolation. Freyr always builds software that is open, interoperable and easily connects with the existing IT systems and your wider network.
intro to solutions
Keeping the following core principles in mind.
- simple, intuitive, light-weight, yet compliant software on the cloud (and on premise)
- built based on best-practices and aggregated pharma industry knowledge from across 500+
- global clients spanning 10 years, including top-20 bio pharma
- next-generation, digital-automation enabled solutions
- seamlessly integrated with actionable regulatory-intelligence
Whether you are a start-up Bio Pharma or an established company with multi-country product portfolio, these solutions are available as standalone products or as a comprehensive, scalable, end-to-end Regulatory Software Cloud capable enough to run your entire Regulatory content workflow.
