Search Harmonised Standards in ASEAN: HS

ACM 001 IDENTIFICATION OF TRETINOIN (RETINOIC ACID) IN COSMETIC PRODUCTS BY TLC AND HPLC / ACM 001

The method describes the identification of retinoic acid in cosmetic products.  [More Details+]

ACM 002 IDENTIFICATION OF PROHIBITED COLORANTS IN COSMETIC PRODUCTS BY TLC AND HPLC / ACM 002

This method describes the identification of the following prohibited colorants in cosmetic products: C I number: Other names : 12075 Pigment Orange 5 13065 Metanil…  [More Details+]

ACM 003 IDENTIFICATION AND DETERMINATION OF HYDROQUINONE IN COSMETIC PRODUCTS BY TLC AND HPLC / ACM 003

The method describes the identification of hydroquinone in cosmetic products.  [More Details+]

ACM 004 IDENTIFICATION AND DETERMINATION OF 2-PHENOXYETHANOL, METHYL, ETHYL, PROPYL, AND BUTYL 4-HYDROXYBENZOATE IN COSMETIC PRODUCTS BY TLC AND HPLC / ACM 004

This method specifies a TLC procedure that, in combination with the determination method described in Section B, allows the identification of 2-phenoxyethanol, methyl 4-hydroxybenzoate, ethyl…  [More Details+]

ACM 006 ENUMERATION OF AEROBIC MESOPHILIC BACTERIA, YEAST AND MOULD / ACM 006

The method specifies the procedure for enumeration of aerobic bacteria, yeast, and mold present in cosmetic products.  [More Details+]

ACM 007 IDENTIFICATION OF STEROIDS IN COSMETIC ODUCTS BY TLC AND HPLC / ACM 007

The method describes the identification of hydrocortisone acetate, dexamethasone, betamethasone, betamethasone 17-valerate and triamcinolone acetonide in cosmetic products.  [More Details+]

ACM 008 EVALUATION OF THE ANTIMICROBIAL PROTECTION OF A COSMETIC PRODUCT / ACM 008

To determine the efficacy of the antimicrobial activity of preservatives used in cosmetic products. The method covers the determination of the suitability of preservation of…  [More Details+]

ACM 009 DETERMINATION OF SALICYLIC ACID (BETA HYDROXY ACID) IN COSMETIC PRODUCTS BY HIGH PERFORMANCE LIQUID CHROMATOGRAPHY (HPLC) / ACM 009

The test method describes the determination of salicylic acid in cosmetic products (cream).  [More Details+]

ACM 010 DETERMINATION OF GLYCOLIC ACID AND LACTIC ACID (ALPHA HYDROXY ACID) BY HIGH PERFORMANCE LIQUID CHROMATOGRAPH(HPLC) USING REVERSED PHASE SYSTEM / ACM 010

The method describes the determination of alpha hydroxyl acid (glycolic acid and lactic acid) in cosmetic products.  [More Details+]

ACM 011 DETERMINATION OF 1,4-DIOXANE IN COSMETIC PRODUCTS BY GAS CHROMATOGRAPHY MASS SPECTROMETRY HEAD SPACE SAMPLER (GC-MS/HSS) / ACM 011

This method specifies a procedure for determination of 1,4-Dioxane in cosmetic products by Gas Chromatography Mass Spectrometry Head Space Sampler.  [More Details+]

Medical devices -- Application of risk management to medical devices / ISO 14971:2007

ISO 14971:2007 specifies a process for a manufacturer to identify the hazards associated with medical devices, including in vitro diagnostic (IVD) medical devices, to estimate…  [More Details+]

Medical devices -- Quality management systems -- Guidance on the application of ISO 13485: 2003 / ISO/TR 14969:2004

ISO/TR 14969:2004 provides guidance for the application of the requirements for quality management systems contained in ISO 13485. It does not add to, or otherwise…  [More Details+]

Medical devices -- Quality management systems -- Requirements for regulatory purposes / ISO 13485:2003

ISO 13485:2003 specifies requirements for a quality management system where an organization needs to demonstrate its ability to provide medical devices and related services that…  [More Details+]

Packaging for terminally sterilized medical devices -- Part 2: Validation requirements for forming, sealing and assembly processes / ISO 11607-2:2006

ISO 11607-2:2006 specifies the requirements for development and validation of processes for packaging medical devices that are terminally sterilized. These processes include forming, sealing, and…  [More Details+]

Sterilization of health care products -- Radiation -- Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices / ISO 11137-1:2006

ISO 11137-1:2006 specifies requirements for the development, validation and routine control of a radiation sterilization process for medical devices. Although the scope of ISO 11137-1:2006…  [More Details+]