We'll explore your initial idea through brainstorming sessions and preliminary design work. I’ll evaluate technical feasibility, manufacturing constraints, and regulatory considerations to guide the concept in the right direction. What you get: - Concept sketches or basic 3D layouts. - Design requirement summary. - Technical feasibility assessment. - Material and manufacturing considerations. - Risk and cost-impact overview.

I’ll transform the concept into detailed engineering models and prototypes using tools like SolidWorks, Inventor, or AutoCAD. Designs will be optimized for DFM/DFA and backed by documentation ready for further development or production. What you get: - 3D CAD models and 2D technical drawings - Assembly structure and BOMs - Tolerance analysis and design iterations - Prototype-ready files (STL, STEP, PDF, DWG) - DFM/DFA recommendations

Based on the intended use and product complexity, I’ll design testing and verification strategies to ensure functionality, compliance, and reliability. Ideal for regulated products including medical devices. What you get: - Test strategy overview (based on standards like ISO 13485, ISO 14971, or IEC 60601) - Custom test plan (mechanical, functional, durability, etc.) - Risk-based validation approach (FMEA-based if applicable) - Recommendations for equipment or setups (lab or field testing) - Test documentation templates (protocols, logs, reports)