Turn compliance obstacles into real business opportunities. Whatever your needs, whether Advisory, Project, or Managed Services, Epista can help. Our pragmatic approach identifies where to set the bar so quality levels fit both your regulatory requirements and your business objectives. We’ll help you figure out where you are now, and where you want to go. Then, we’ll help you get there – and stay there.
Regardless of whether your business is large or small, Pharmaceutical, Biotech or Medical Device, Epista can help with all facets of your compliance and IT projects.
Our subject matter expertise supports Pre-Clinical, Clinical, R&D, Manufacturing, Regulatory Affairs, IT and QA. We know the specific priorities of each part of your company, so we bridge the gap between IT, QA and Line-of-Business.
We support customers in Europe, North America and Asia, and have local offices in Denmark, Germany and Sweden.
General VAR Agreement
When selecting, implementing and operating 3DS solutions, Epista Life Science support customers by Subejct Matter Expertise and Advisory within the system, business procss optimization and continuous compliance.