- Faisal Minhas
- Director
Description
Consulting Services in following areas:
- Management System development and implementation services in order to comply to Canadian Medical Device Regulations CMDR ) and ISO 13485:2003 ( CMDCAS ) requirements
- to achieve certification and comply to ISO 9001:2000, ISO 13485:2003, ISO 14000, FDA's QAS and European Medical Device Directive (covering CE requirements)
Internal Audit:
- perform first and second party audits covering sub-contractor control audits
Training :
- Public and in-house customize trainings
ISO Software:
- One of most user friendly and productive software to compliment your ISO system
Job Placement:
- Provide competent workforce as per our client's set expectations
Company contacts
Products & services
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