PROGRAM PEMBANGUNAN USAHAWAN

PENTING PROGRAM PEMBANGUNAN USAHAWAN UMMAH SYNERGY VENTURES MENCARI CALON USAHAWAN UNTUK DIBANGUNKAN DALAM PROGRAM KEUSAHAWANAN SKOP: PROPOSAL KEUSAHAWANAN (PELBAGAI BIDANG) KELAYAKAN: BERUMUR TIDAK LEBIH 50 TAHUN TAHAP PENDIDIKAN SEKURANG-KURANGNYA SPM PENGALAMAN: SEKURANG-KURANGNYA 3 TAHUN PENGALAMAN DALAM BIDANG YANG DIPILIH BANTUAN: KEMUDAHAN PINJAMAN/ GERAN KEMUDAHAN PEMBIAYAAN BERSAMA DENGAN KERJASAMA UMMAH SYNERGY VENTURES (USV) DANA BULANAN UNTUK “WORKING CAPITAL” BANTUAN TEKNIKAL HUBUNGI KAMI 03-3362 3502 017-2130501 (whatsapp)

GERAN UNTUK PERSIJILAN GDPMD

GERAN PERSIJILAN GDPMD  untuk 50 buah syarikat berkaitan Barangan Perubatan. Hubungi segera: e mail: sales.ummahsynergy@gmail.com UMMAH SYNERGY VENTURES 03-3362 4502

MALAYSIA STANDARD ONLINE

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Latest List of CAB for GDPMD and Medical Device Registration

ISO 9001:2015 SEMINAR REGISTRATION

ISO 9001:2015 SEMINAR REGISTRATION FORM - click HERE!

NEW ISO 9001: 2015 UPDATE TRAINING

SEMINAR ON REGISTRATION OF MEDICAL DEVICE

SEMINAR ON REGISTRATION OF MEDICAL DEVICES

Registration of Medical Device is mandatory base on Medical Device Act 737, 2012. Part II, registration of medical device and conformity assessment body “Requirement for Registration of medical device Part 5 (1) No medical device shall be imported, exported or placed in the market unless the medical device is registered under this Act.”

Overview: Medical device product registration had been a hot topic among the stake holder ever since the Medical Device Act 737, gazetted and its requirement for all medical device related supplier or importer to register. It had been a concern on the safety and performance of medical device being used and already widely circulated in the country. Since no act had governing the supply and activity regarding the medical devices  supply chain, registration of medical device will be a move to ensure all medical device being circulated and distributed in the country  had undergone strict evaluation and monitoring, especially from the regulatory body, MDA.

The Topics: To make awareness of the registration approach Understanding the documentation requirement Compliance with product safety and performance Understanding CAB assessment requirements Consequences of product sold without registration The Fast Tract approach.

Speaker: MDA official (To be advice) CAB representative TBA

Who Should attend: Medical Device LAR Medical device Importer Medical Device distributor Medical Device Manufacturer Target audience: 100 pax

Date and Time: Date: 15/8/2015   Time: 9.30am - 1.00pm Duration: 1/2 day

Location: Ballroom, Hotel,  Shah Alam

Fee: RM 168 per pax. E- mail your enquiry to: sales.ummahsynergy@gmail.com @ booking at 03 7831 8502 (IZA)