IZiel Healthcare is an Engineering & Regulatory Services provider working successfully for global medical device manufacturers from our offices in USA & India. Our engineers are trained as per Design for Six Sigma – Black Belt Level and have completed various projects in Design, Process Validation, QMS Documentation, Regulatory Approvals & Acquisition Integration for Class I, IIa, IIb & III Products.
We leverage statistical & data-driven methods, domain knowledge & robust work planning methodology to achieve an optimized product development processes for guaranteed success.
IZiel Healthcare provides services in:
Design
- Systems Engineering and Requirements Management
- Transfer Function Development
- Predictive Engineering
- 3D Modelling & Finite Element Analysis (FEA)
- Design Controls
Process & Software Validation
- PVMP
- IQ, OQ, PQ
- Test Method Validation (TMV)
- Productivity Improvement
- Software Validation (IEC 62304)
Risk Management
- ISO 14971 based Risk Management
- FMEA and FTA Based Product Risk Analysis
- Quantitative Risk Management Expertise
Quality Management Systems and CAPA
- QMS Documentation with Procedures & Templates
- CAPA (Corrective & Preventive Action)
Regulatory
- USFDA & CE Approvals
- MDD – MDR Conversion
- Clinical Evaluation Report (CER)
- European Authorised Representative (EAR)
Remediation
- Resolve Observations (Form 483), Warning Letters etc
- Product Remediation
Training
- Training – DFSS Methodologies and Engineering Topics
Industry
Medical Equipment Manufacturing
HQ Location
14, Hadapsar Industrial Estate
Hadapsar
Pune, Maharashtra 411013, IN
Keywords
Medical Device DesignDesign EngineeringProcess DevelopmentProcess EngineeringDesign ValidationProcess ValidationRisk ManagementMarket Developmentand Regulatory Services