During a half-day session, we figure out where your processes are holding you back — and what’s required for your ERP system to keep pace with your commercialization.
Tailored to your business and your processes
Focus on business value and compliance readiness — not technology
Conducted with Implema and Epista Life Science
Life Science companies in growth phases face a well-known pattern: the processes that worked a year ago don’t hold up to regulatory requirements, international expansion, and increased volume. The result is manual work, delayed batch releases, and compliance risks — which show up directly on the bottom line.
Batch release takes too long Manual flows and fragmented systems mean release cycles that should take days take weeks — slowing down your revenue.
Regulatory requirements are increasing FDA, EMA, and GxP require traceability and documentation that many companies can’t handle with existing systems and workflows.
Manual work ties up resources Up to 40% of working hours in regulated companies are spent on manual data collection and reporting. These are resources that should be spent on business development.
Commercialization requires scalability New markets, more products, and partnerships expose every flaw in your processes. Systems must keep up — not hold you back.
The workshop is relevant for decision-makers in Life Science companies in growth or commercialization phases. Typical participants are CFOs, COOs, IT Managers, QA/Regulatory Affairs Managers, and Operations Managers. Three to four people from your side is usually a good number.
No. The workshop is just as suitable if you have an existing system you’re unhappy with, if you’re about to decide on a new ERP system, or if you’re in the middle of a project and want an independent second opinion.
No. The workshop is a structured analysis — we map your situation and provide you with an objective basis for decision-making. You decide if and how you want to move forward. The final module contains recommendations, but no sales.
The workshop is free of charge. You invest a half-day — we deliver a basis for decision-making that you can actually use.
Epista is our partner with specialist knowledge in GxP, FDA/EMA requirements, and regulated processes. Together, we cover the whole picture: ERP expertise and regulatory competence in the same workshop.
We implement Microsoft Dynamics 365 with a deep understanding of GxP requirements, batch release, quarantine management, and regulatory traceability. It's not a standard implementation — and we don't treat it like one.
Calliditas Therapeutics was FDA-ready in 9 months with Dynamics 365. Atlas Antibodies drives its global growth — 60,000+ products, exports to 60+ countries — on a system we implemented and continue to manage.
Together with Epista, we combine ERP expertise with regulatory specialist knowledge. One team, one responsibility — from workshop to go-live.
We always work according to our proven delivery model: fast decisions, standardized processes, and business value at the center. This also applies to the workshop — clear structure and concrete deliverables.
Practical tips, inspiration, and insights from our experts – for those who want to stay ahead.
Register your interest and get a concrete basis for decision-making on how to strengthen your compliance readiness and scale your processes.
Key Account Manager Dynamics
Get a concrete starting point for how to streamline your Life Science processes and strengthen your compliance readiness. In the workshop, we map your current state, identify gaps, and set a clear plan for how you create business value — faster.
