ISO 13485 certificate & ISO 13485 consultants for ISO certification. ISO 13485 certificate consultants and training in Delhi
Whatever devices organization's produce, as medical device manufacturer/s, they have the responsibility to consistently deliver devices that are safe and effective. ISO 13485 is the international standard recognized for medical device regulations around the world.
Gaining certification to ISO 13485 will help organization do business in this highly regulated sector. Whether organizations are looking to operate internationally or to expand locally to accommodate new business, ISO 13485 will help demonstrate to customers and regulators that they are committed to quality.
The regular assessment process will ensure that processes are continually checked for effectiveness and provide the opportunity to avoid unpleasant regulatory surprises. Certification to this standard can improve overall performance, remove uncertainty and widen market opportunities with complying to requirements
As a partner in quality, the company helps suppliers and OEMs identify root cause of quality problems, minimize defects, improve quality, increase efficiency and reduce costs associated with quality issues.
Lakshy Management Consultancy is a leading provider of quality assurance and outsourcing solutions to manufacturers of parts and components in the automotive, medical device, electronics, home appliance and recreational vehicle industries.
Lakshy Management Consultant Pvt. Ltd. ISO 13485 QMS Implementation Support is loaded with advantages for your organization. Basic Support provides a process- based, documented, implemented, audited Quality Management System (QMS), acknowledging all ISO 13485 quality requirements, ready for certification.
ISO 13485 requirements (no "gap assessment" required) documentation and implementation support for your value added quality management system development of a simple, effective document and record control system training of an Internal Quality Audit Team, if you choose a mentored, full system audit of the new quality management system (no registrar "preliminary assessment" required) corrective/preventive action support from the full system audit recommendation for an economical, effective registrar, if you choose our witness of your registration audit, if you choose We take the time necessary to custom fit all applicable ISO 13485 requirements to your organization. No "consultant" is as willing and able as Lakshy Management Consultant Pvt. Ltd. to take the time to build a QMS to both reduce your costs and "pass the audit," guaranteed.
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