Consultation and Training in Medical Devices
Expert in ISO 13485, GDPMD, MDA Regulatory Requirements, CE marking, FDA related and Medical Device Related Requirements
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Wednesday
Ethylene Oxide Sterilization Validation
ISO 9001:2015 CONTEXT OF ORGANIZATION
ISO 9001:2015 RISK BASE THINKING
Thursday
BUSINESS ACCELERATOR PROGRAMME : SMECORP
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Wednesday
ISO 9001: 2015 TRAINING
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Thursday
SEMINAR ON FACILITATION & CONSULTATION TO IMPROVE QUALITY MANAGEMENT SYSTEM
You are cordially invited to join us for a free seminar on ‘Facilitation & Consultation to Improve Quality Management System’.
An effective quality management system is a rigorous process to continually increase quality values of products and services in a company as well as the economy. Therefore, useful knowledge pertaining available funds from relevant agencies is also vital for financial support.
Seating is
limited for 25 seats
and it is first come first served basis. Lunch is
provided
. Any cancellation must be made before
12
th
October 2016
to avoid any inconvenience or miscommunication matters.
Sign-up the registration form attached and send back to us as soon as possible to reserve your seats. We are pleased to see you on that day.
GDPMD MANUAL AND GUIDELINES
FDA GUIDELINE FOR MEDICAL EXAMINATION GLOVE
VALIDATION OF PROCESS - PHARMACEUTICAL
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