Med Device | Pharma | Semiconductor | Electronics
Carry a governed design into planning, simulation, and electronic work instructions—variant-true and audit-ready—so regulated manufacturers hit throughput without late surprises.
Speed with Control in Regulated Manufacturing
In regulated manufacturing, speed and control are not opposites—they’re cause and effect. The products change (drug-device combinations, implantables, wafer tools, SMT lines, smart appliances), but the root failure is familiar: design and planning aren’t looking at the same truth. One team approves a concept; another discovers reach, cycle, or instruction gaps after release. The fix is carrying a governed definition—variants, effectivity, redlines—straight into planning, simulation, and electronic work instructions (EWIs), and keeping that thread intact as changes land. Teamcenter makes this flow practical.
Start with the EBOM as your source of truth. Options (market, kit, regulatory) and effectivity (date/lot/serial) live on governed items, not in side spreadsheets. When you baseline a release, you freeze that variant-true definition and the rationale behind it. Planning then aligns EBOM parts to manufacturing context—stations, resources, operations—to author the MBOM and BOP. From there, two accelerators kick in: simulation to catch problems before they hit the floor, and EWIs that reflect the exact configuration operators will see.
Simulation isn’t academic—it’s an insurance policy you cash every day. In electronics assembly, small fixture or reach issues cascade into missed takt; in pharma packaging, micro-delays at one step starve the downstream cell; in semiconductor handling, a millimeter of clearance can make or break throughput. With Teamcenter-connected tools you can load a configured study (the exact market/model/lot you’ll build), test feasibility, and write the proven steps back into the BOP so your plan and your reality match. Customers who push validation upstream report substantial reductions in on-site commissioning time and rework; across industries, we see 30–70% reductions once virtual checks precede the build.
Authoring and balancing are where regulated teams reclaim hours. Easy Plan has matured to help planners work at speed without losing control: line balancing compares bottleneck vs. takt, with configurable KPI dashboards that surface what to fix first; Focus Mode and column presets reduce clutter for high-mix products; and change-driven effectivity keeps applicability honest. Instead of re-authoring after each ECO, planners absorb deltas that arrive with the right variant scope baked in. The payoff shows up as smoother handoffs and calmer launches.
EWIs are the visible end of the thread. Using Rapid Author, teams generate visual, step-by-step instructions directly from the BOP—so when a design change lands or a market option toggles, the instruction updates with it. That’s especially valuable in med device and pharma where training, traceability, and right-first-time are audited outcomes. Operators get the correct sequence for this lot; quality sees alignment between what was approved and what was built; audit prep stops being an archeological dig.
Simulation at the factory-flow level matters, too. With Plant Simulation connected to Teamcenter, you can model line capacity, buffers, and logistics using the same structures (BOM/BOP/BoE) and JT geometry. Teams have documented energy and resource reductions as well as cycle-time improvements by testing scenarios virtually—valuable in semiconductor cleanrooms and high-energy processes where utilities like nitrogen are non-trivial costs. The common thread is that the model reflects the governed definition, not a fictional average.
Real programs tell the story better than any brochure. In electronics and medical assembly, customers using simulation and governed handoffs report shorter project timelines and meaningful throughput gains; one semiconductor flow documented −5% electricity, −10% nitrogen, and +15% production efficiency after optimizing with Plant Simulation—wins that start with a model connected to the real product and processes. The domains differ; the pattern holds.
You can adopt this without boiling the ocean:
Pick one high-risk product family
e.g., catheter assemblies, vial packaging, wafer FOUP handling, or a complex PCB. Baseline the EBOM with options/effectivity and publish the rationale.
Load a configured study
for that exact baseline into simulation. Validate reach, clashes, ergonomics, and cycle. Publish a one-page delta list.
Absorb deltas into the BOP
and run a line balance against the intended mix. Capture the KPI snapshot (bottleneck vs. takt) to guide fixes.
Publish EWIs
from the updated BOP using Rapid Author. Train one cell; measure error rates and time-to-approve versus your current baseline.
Ready to pilot in your environment?
Regulated Design→Planning Pilot Kit
NEWa two-week plan with baseline steps, simulation checks, BOP/EWI deliverables, and review cadence tailored to med device, pharma, semi, and electronics.
Request the Throughput & Commissioning Calculator : estimate cycle-time impact and commissioning reduction when you connect governed design, simulation, and EWIs for one product family. Then pair this with Change Management 101 and Variants & Effectivity to keep applicability tight as scope evolves
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