Our Berlin manufacturing workflow projects connect three layers: sensor and vision systems on the production line, the MES (Manufacturing Execution System) for production orchestration, and the ERP for business-level planning. For visual quality inspection: industrial cameras (2D and 3D, using GigE Vision or USB3 Vision standards) capture images of every component at critical inspection points. Our computer vision models — trained on the client's actual defect library — classify each component as pass/fail and categorize defect types (scratch, dent, porosity, dimensional out-of-tolerance, color deviation, assembly error). Training requires 500-2,000 labeled defect images per category for reliable detection; we work with the client's quality team to build this dataset from historical quality records and controlled defect samples. When the AI detects a defect trend (three similar defects in the last 100 components, up from a baseline of one per 500), the workflow kicks in: alert sent to the shift supervisor with the defect pattern and suspected root cause (based on correlation with machine parameters — if defect type X increases when spindle temperature exceeds Y, that correlation is learned and reported), machine parameter adjustment recommended or executed automatically (depending on the client's comfort level with closed-loop control), quality hold placed on potentially affected components downstream, and the entire event documented in the QMS (typically CAQ AG or Babtec, the dominant German quality management systems). Integration with German manufacturing IT is critical: we connect via OPC UA (the industrial communication standard that virtually all modern German manufacturing equipment supports), interface with SAP PP (Production Planning) and SAP QM (Quality Management) for business-level integration, and feed data into MES platforms (MPDV Hydra, FORCAM FORCE, iTAC — the major German MES systems). For pharmaceutical manufacturing, we build GMP-compliant workflow automation: electronic batch records, deviation management workflows, and environmental monitoring with automated alert escalation — all producing documentation that satisfies GMP Annex 11 requirements for computerized systems.