(GDPMD) applies to all companies carrying out activities, as stated in the Medical Devices Act 2012 (Act 737). Malaysian Medical Devices Act 2012 (Act 737) requires all the medical devices manufactures, exporters, importers, distributors, and local authorized representatives to be certified to a Medical Device Quality Management System or Good Distribution Practices for Medical Devices (GDPMD) and register their products as part of the Medical Devices, effectively enforced on 1st July 2013

Section 10 of Medical Device Act ( Act 737 ) requires a medical device to undergo conformity assessment by a registered CAB prior to its registration. However, many medical devices have undergone conformity assessment and approved in countries recognized by Medical Device Authority (MDA).

The Malaysian Sustainable Palm Oil (MSPO) Certification Scheme is the national scheme in Malaysia for oil palm plantations, independent and organised smallholdings, and palm oil processing facilities to be certified against the requirements of the MSPO Standards.

ISO 37001/ MS ISO 37001 is a voluntary internal control system for organizations to manage, handle, enforce, evaluate as well as to improve anti-corruption measures effectively. It is a flexible instrument that can be adapted to decrease the corruption risks faced by any organizations.

IATF 16949:2016 is the International Standard for Automotive Quality Management Systems.

ISO 9001 is defined as the international standard that specifies requirements for a quality management system (QMS).consectetur ullamcorper.

The goal of ISO 45001 is the reduction of occupational injuries and diseases, including promoting and protecting physical and mental health.

MS 4R2S is a qualification and standardization of automotive parts and components to enhance and standardize the Reuse, Recycle, Remanufacturing, Repair, Services and Spare part sectors of the Automotive Industry.

ISO 13485 is an Internationally Recognized Quality Standard which states the requirements of the Quality Management System (QMS) for the design and manufacture of Medical Devices.

ISO 22000 is a globally recognised standard for food safety in all links of the food chain. It was developed by the International Organization for Standardization (ISO).

GMP describe the conditions and practices that are necessary for the manufacturing, processing, packing or storage of food to ensure its safety and wholesomeness.

ISO 14001:2015 specifies the requirements for an environmental management system that an organization can use to enhance its environmental performance.

Hazard Analysis and Critical Control Point (HACCP) is a systematic approach to identifying and controlling hazards (i.e. microbiological, chemical or physical) that could pose a danger to the preparation of safe food.

The FSSC 22000 Scheme is founded on ISO standards and, just like ISO 22000, focuses on the continuous improvement of a Food Safety Management System.

ISO 50001 Energy Management System is an international standard. The standard specifies the requirements for establishing, implementing, maintaining and improving an energy management system, whose purpose is to enable an organization to follow a systematic approach in achieving continual improvement of energy performance, including energy efficiency, energy security, energy use and consumption.

The international standard ISO 27001 sets out the requirements for an information security management system (ISMS). With an ISMS, you can secure sensitive information using a systematic approach that covers people, processes and IT systems.