- Qualifying Examination to Practice Pharmacy
- Medicine Advertisements Board
- List of Training Premises for Provisionally Registered Pharmacist (PRP)
- Notification of Contract for the Supply of Security Labels and Management of the Pharmaceutical Track & Trace System (PTTS) for Pharmaceutical Products Registered with the Ministry of Health Malaysia (MOH)
- Garis Panduan Petugas Haji Malaysia Rombongan Perubatan (Perkhidmatan Farmasi)
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This is not allowed. Any amendment on the advertisement format must be approved by the MAB before advertised to the public.
Kategori: Soalan Lazim | Tarikh: 09 Feb 2024
Pemohon dikehendaki memohon kelulusan daripada LIU bagi sebarang pindaan yang ingin dilakukan ke atas format iklan yang telah diluluskan. Prosedur untuk permohonan pindaan adalah seperti berikut:...
Kategori: Soalan Lazim | Tarikh: 09 Feb 2024
The applicant is required to get approval from MAB for any amendments intended for the approved advertisement format. The procedures for applying amendments are as follow: Applicants are...
Kategori: Soalan Lazim | Tarikh: 09 Feb 2024
Piagam pelanggan kelulusan iklan daripada LIU adalah 5 hari bekerja bagi format iklan selain laman sesawang manakala 30 hari (termasuk hujung minggu dan cuti umum) bagi format iklan laman sesawang.
Kategori: Soalan Lazim | Tarikh: 09 Feb 2024
The client charter of advertisement approval from MAB is 5 working days for advertisement format other than website while 30 days (including weekends and public holidays) for website format.
Kategori: Soalan Lazim | Tarikh: 09 Feb 2024
Semua jenis media penyiaran yang bertujuan untuk mempromosikan atau menyebarkan maklumat berkenaan produk ubat berdaftar dan perkhidmatan kesihatan bagi menarik perhatian umum boleh diklasifikasikan...
Kategori: Soalan Lazim | Tarikh: 20 Feb 2024
All types of dissemination of information about products and healthcare services to attract public attention, including on the internet, are classified as an advertisement. As stated in Section 4B...
Kategori: Soalan Lazim | Tarikh: 20 Feb 2024
Garis panduan ini digunapakai untuk pembangunan fasiliti bilik bersih Cytotoxic Drug Reconstitution (CDR) dan Non-CDR
Kategori: Dokumen | Tarikh: 29 May 2017
This guideline is used as a reference in the development of clean room facilities for Cytotoxic Drug Reconstitution (CDR) and Non-CDR
Kategori: Dokumen | Tarikh: 19 Nov 2013
Proses penyerahan MoA yang telah ditandatangani di antara Kementerian Kesihatan Malaysia dengan Institusi Pengajian Tinggi tempatan bagi membolehkan pelajar ijazah farmasi dari Institusi...
Kategori: Album | Tarikh: 27 Jan 2013