Services
NYQC provides varieties of services including Internal Quality Audits, Training,
Supplier Audits and Market Access and Device registration
ISO 9001:2015
Is a Quality Management Standard which stipulates requirements for Quality Management Systems. The standard helps businesses and companies to improve efficiency and enhance customer satisfaction and services. Also, the standard focuses on continual improvement
MDSAP TRAINING
The MDSAP was implemented-based on requirements that are defined in the IMDRF MDSAP Model; Five participating countries – Australia, Brazil, Canada , Japan and the USA.
Regulatory authorities:- TGA
- ANVISA
- Health Canada
- MHLW/PMDA
- FDA
ISO 13485:2016
ISO 13485, Medical devices – Quality management systems – Requirements for regulatory purposes, is an internationally recognized standard which sets out the requirements for a quality management system specific to the medical devices industry.
The Standard specifies requirements for a quality management system where an organization needs to demonstrate its ability to provide medical devices and related services which consistently meet applicable regulatory requirements and customer requirements.
REGULATORY AFFAIRS
- Regulatory strategy development
- Agency Interactions
- Marketing approvals
- Licensing renewals and submissions
Our Expertise
01. Implementation of ISO 9001:2015
- Service and Manufacturing Industry
- Gap Analysis audit
- Supplier audits
- Training – Onsite and Remote training
02. Implementation of ISO 13485:2016
- Gap Analysis audits
- Supplier Audits
- Internal Quality Audits
- Risk Management
03. Implementation of ISO 17025
- Training
- Gap Analysis
- Supplier Audits
- Internal Quality Audits
04. MDSAP
- Training
- Gap Analysis
- Internal Quality Audits
05. EU MDR
- Gap Analysis
- Training
- Internal Audits
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Address
Ottawa, Ontario, Canada
Call Us
+1 613 804-8674
Email Us
info@nyqc.ca
Nazeer Yakoob