Our state-of-the-art facilities adhere to stringent international and local standards, ensuring safe, efficient, and eco-friendly production processes:
Good Manufacturing Practice (GMP) for cosmetics sets the standard for how a factory is actually run — covering personnel, premises, equipment, documentation, production and quality control. In Malaysia, cosmetic GMP follows the ASEAN Guidelines for Cosmetic Good Manufacturing Practice, and manufacturers are assessed by the National Pharmaceutical Regulatory Agency (NPRA), the arm of the Ministry of Health that regulates cosmetics. Working with a GMP manufacturer is what allows your finished product to be notified with the NPRA and sold legally in Malaysia. It is also the baseline evidence export markets and retail buyers ask for before they will list a product.
Held by Dr Orizi (M) Sdn. Bhd.
Verify: NPRA cosmetic manufacturer register.
Good Manufacturing Practice for food covers the hygiene, process control and traceability standards a food factory must meet — from raw material handling through production, packing and storage. In Malaysia it is certified against MS 1514, with certification issued by bodies such as SIRIM QAS International and the Ministry of Health Malaysia. It means your supplement, food or beverage is produced under audited controls rather than trust alone. For a brand owner, it is the documentation distributors and retail buyers expect to see before listing a product.
Held by D&O Nutraceutical Manufacturing Sdn. Bhd. (SIRIM QAS, MS 1514:2022, cert. GMP 00203) and Nutrizens Wellness Sdn. Bhd. (Ministry of Health Malaysia, cert. GM0226016-0/1).
ISO 22716 is the international Good Manufacturing Practice standard for cosmetics, published by the International Organization for Standardization (ISO). It gives practical guidance on production, storage, packaging, testing and transportation — effectively the global counterpart to the ASEAN cosmetic GMP guidelines. It is recognised in the European Union as the reference GMP standard for cosmetic products. For brand owners selling beyond Malaysia, ISO 22716 is often the standard an overseas buyer or regulator names directly.
Held by Dr Orizi (M) Sdn. Bhd.
ISO 22000 is the international standard for food safety management systems, published by the International Organization for Standardization (ISO). It combines HACCP principles with a full management system covering communication, hazard control and continuous improvement across the supply chain. Unlike a one-off hygiene inspection, it is audited by an accredited certification body and reassessed on a regular cycle. For a brand owner it is recognised, exportable proof that food safety is managed systematically rather than ad hoc.
Held by D&O Nutraceutical Manufacturing Sdn. Bhd. (SIRIM QAS, cert. FSMS 00229) and Nutrizens Wellness Sdn. Bhd. (SIRIM QAS / IQNET, cert. FSMS 00253).
HACCP is a preventive food safety system: it identifies where contamination could occur, sets critical control points, and monitors them continuously instead of relying on end-product testing. The framework is recognised internationally through Codex Alimentarius and, in Malaysia, certified against MS 1480 by bodies such as SIRIM QAS International and the Ministry of Health Malaysia. It underpins ISO 22000 and is frequently a prerequisite for export and for supplying larger retailers. For your brand it means hazards are controlled during production, with records to prove it.
Held by D&O Nutraceutical Manufacturing Sdn. Bhd. (SIRIM QAS, MS 1480:2019, cert. HACCP 00425) and Nutrizens Wellness Sdn. Bhd. (Ministry of Health Malaysia, cert. HA1225012-0/1).
ISO 13485 is the international quality management system standard written specifically for medical devices, published by the International Organization for Standardization (ISO). It goes beyond general quality management by requiring risk management, design controls, traceability and sterility assurance appropriate to devices. In Malaysia it is assessed by a Conformity Assessment Body registered with the Medical Device Authority, and holding it is a condition of keeping a manufacturer’s establishment licence. For a brand owner it is the system evidence that sits behind any device registration.
Held by Imedify Medical Solution Sdn. Bhd. (cert. 510632) and Skyler Medical Manufacturing Sdn. Bhd. (cert. 510512), both assessed against ISO 13485:2016 by KGS Certification Sdn. Bhd..
Verify: MDA licensed establishment register.
MeSTI (Makanan Selamat Tanggungjawab Industri — “safe food is the industry’s responsibility”) is Malaysia’s food safety scheme, administered by the Food Safety and Quality Division of the Ministry of Health Malaysia. It requires food premises to meet defined hygiene, process control and traceability requirements, and is a legal prerequisite for manufacturing food in Malaysia. Certificates are issued and listed through the Ministry’s FoSIM system. For a brand owner it confirms the facility making your product is licensed to do so.
Held by D&O Nutraceutical Manufacturing Sdn. Bhd. (cert. ME0523069-0/1) and Nutrizens Wellness Sdn. Bhd.
Verify: FoSIM (Ministry of Health).
The Net Energy Metering (NEM) programme is administered by the Sustainable Energy Development Authority (SEDA) Malaysia and allows a facility to generate its own solar power and export the surplus to the national grid. NEM NOVA is the scheme tier open to commercial and industrial users. It means a share of the energy used to make your product is generated by solar on our own roof rather than drawn from the grid. For brand owners with sustainability or carbon reporting obligations, that is a measurable supply chain input.
Held by Dr Orizi (M) Sdn. Bhd.
SA8000 is an international social accountability standard developed by Social Accountability International (SAI), covering child labour, forced labour, health and safety, freedom of association, discrimination, working hours and fair pay. It is independently audited and requires a functioning management system, not simply a signed policy. It is one of the most widely recognised ethical manufacturing certifications in the world. For a brand owner it is third-party evidence that the people making your product are treated lawfully and fairly — increasingly a condition of doing business with larger retailers.
Held by Dr Orizi (M) Sdn. Bhd. — certificate IAS/MYS/10152, issued by UQAS.
Sedex (Supplier Ethical Data Exchange) is a global platform used by brands and retailers to share and assess ethical supply chain data. Members maintain a site profile covering labour standards, health and safety, environment and business ethics, which customers can review directly on the platform. Membership is also a prerequisite for undergoing a SMETA audit. For a brand owner it means our site data already sits on the platform your procurement or compliance team most likely uses.
Held by Dr Orizi (M) Sdn. Bhd. — Sedex ZS number ZS416762168.
Pioneer Status is an incentive granted by the Malaysian Investment Development Authority (MIDA) to companies engaged in promoted activities or products, typically involving advanced technology or a significant contribution to industrial development. It carries partial exemption from income tax on statutory income for a defined period. It is granted selectively and is assessed on the nature of the manufacturing activity itself. For a brand owner it signals that the facility making your product has been recognised by the Malaysian government as a technology-led operation.
Held by Skyler Medical Manufacturing Sdn. Bhd.
The Healthier Choice Logo (HCL) is a government-endorsed symbol controlled by health authorities, such as Malaysia’s Ministry of Health. It certifies that a product meets strict nutritional criteria like lower fat, sugar, or sodium, helping consumers easily identify and choose healthier food and beverage options.
Under the Modernization of Cosmetics Regulation Act (MoCRA), any facility manufacturing cosmetics for the United States market must register with the U.S. Food and Drug Administration (FDA) and list its products. Registration gives the FDA visibility of the facility and must be renewed periodically. It is a mandatory filing step for placing cosmetic products on the U.S. market, and a facility that is not registered cannot legally supply it. For a brand owner it means a U.S. launch does not stall waiting for the factory to be registered.
Held by Dr Orizi (M) Sdn. Bhd. — FDA Establishment Identifier (FEI): 3041511808.
Facility registration is a filing requirement; it is not an FDA approval or endorsement of the facility or its products.
The D-U-N-S® Number is a unique nine-digit business identifier issued by Dun & Bradstreet and used worldwide to verify a company’s identity, corporate structure and credit standing. It is requested by many international buyers, banks, online platforms and government procurement systems as a basic due diligence check. It confirms that a company exists as a distinct, traceable legal entity. For a brand owner it makes verifying exactly who you are contracting with straightforward.
Held by Dr Orizi (M) Sdn. Bhd. — D-U-N-S number 66-058-7789. Also held by D&O Nutraceutical Manufacturing Sdn. Bhd. — D-U-N-S number 47-325-1431.
SMETA (Sedex Members Ethical Trade Audit) is the most widely used social audit in the world, powered by Sedex. It assesses a site against the ETI Base Code and International Labour Organization conventions, covering labour standards, health and safety, environment and business ethics. SMETA is an audit rather than a certification: it produces a detailed report and corrective action plan shared on the Sedex platform, which customers can review directly. For a brand owner it means an independent auditor has walked our floor and the findings are open to you, not summarised by us.
Held by Dr Orizi (M) Sdn. Bhd. — SMETA audit reference ZAA600170493, conducted by Intertek.
Under the FDA Food Safety Modernization Act (FSMA), any foreign facility manufacturing food for the United States market must register with the U.S. Food and Drug Administration (FDA) as required by 21 CFR Part 1, Subpart H, and the Public Health Security and Bioterrorism Preparedness and Response Act of 2002. Registration must be renewed on a biennial cycle. It is a mandatory filing step for placing food products on the U.S. market, and a facility that is not registered cannot legally supply it. For a brand owner it means a U.S. food launch does not stall waiting for the factory to be registered.
Held by D&O Nutraceutical Manufacturing Sdn. Bhd. — US FDA Registration Number: 14791969014.
Facility registration is a filing requirement; it is not an FDA approval or endorsement of the facility or its products.
We ensure that our products meet specific regulatory, safety, and quality standards for both local and international markets:
Malaysian Halal certification is issued by the Department of Islamic Development Malaysia (JAKIM) and is among the most widely recognised Halal schemes in the world. It covers ingredients, processing aids, equipment, cleaning, storage and the entire production chain — not merely the recipe. Cosmetics are certified to MS 2634 and food to MS 1500, each with its own audited requirements. For a brand owner it opens the Muslim consumer market in Malaysia and is frequently recognised or accepted across ASEAN and Gulf export markets.
Held by Dr Orizi (M) Sdn. Bhd., D&O Nutraceutical Manufacturing Sdn. Bhd., Nutrizens Wellness Sdn. Bhd. and Skyler Medical Manufacturing Sdn. Bhd.
Verify: JAKIM MYeHALAL directory.
Any company that manufactures, imports or distributes medical devices in Malaysia must hold an establishment licence from the Medical Device Authority (MDA) under the Medical Device Act 2012 (Act 737). The licence covers the company and its facility, and is granted subject to a valid quality management system certificate from an MDA-registered Conformity Assessment Body. It is separate from device registration: the licence covers the establishment, while each individual device is registered in its own right. For a brand owner it means your device can be legally manufactured and placed on the Malaysian market.
Held by Imedify Medical Solution Sdn. Bhd. (licence MDA-7882-K125) and Skyler Medical Manufacturing Sdn. Bhd. (licence MDA-7783-K125).
Verify: MDA licensed establishment register.
Comprehensive testing to confirm that medical devices are safe and non-toxic when used in contact with human tissue, meeting MDA and international standards (ISO 10993).
Verifies that disinfectants effectively eliminate bacteria, viruses, and fungi, meeting international standards for efficacy and safety.
Recognizes our products as proudly made in Malaysia, reflecting local expertise and quality.
Verifies the composition, quality, and compliance of each product batch to ensure it meets the required standards.
Provides essential safety information on ingredients and formulations for safe handling and use.
Confirms the origin of products, enabling smooth international trade and compliance with import/export regulations.
Certifies that products meet the regulatory requirements of their country of origin and are freely sold in the market.
Certifies the use of sustainable packaging materials sourced from responsibly managed forests.
We conduct comprehensive testing to ensure food safety and quality. This includes Nutrition Fact Analysis for accurate labeling of macronutrients and micronutrients, Glycemic Index (GI) Testing for diabetic-friendly products, allergen Testing to identify common allergens and mores.
Guarantees compliance with safety standards, ensuring products are free from harmful contaminants.
Includes safety, efficacy, and shelf-life testing by accredited laboratories to ensure product reliability and consistency.
We ensure our products are secure and stable during transport through various tests. Drop Tests verify packaging resilience to impacts, Compression Tests assess durability under stacking pressure, and Seal Integrity Testing ensures leak-proof seals. Additionally, Temperature and Humidity Testing confirms that products remain stable across different environmental conditions.
Backed by certifications like ECOCERT, USDA Organic, and COSMOS Natural for raw materials sourced from trusted suppliers.
Guarantees that ingredients are non-genetically modified and free from common allergens, meeting consumer demands for clean and safe products.
Certified by suppliers to ensure no animal-derived ingredients or testing are involved in the production process.
Have a question or want to discuss your product ideas? Contact us today, and our team will be happy to assist you.
