By the Relevant Authorities
Revery operates in full compliance with Malaysia’s healthcare, pharmaceutical, and wellness regulations, ensuring every product, service, and treatment meets strict national standards. Our facilities, processes, and formulations are backed by the necessary licences, permits, and professional certifications required by local authorities. This commitment to regulatory excellence reflects our dedication to safety, quality, and ethical practice — giving our clients complete confidence in the integrity and reliability of every Revery experience.
• Status: Bumiputera-certified supplier.
• Purpose: Enables participation in government tenders and contracts.
• Scope: Medical devices, pharmaceuticals, healthcare services.
• Regulator: Ministry of Health Malaysia under the Medical Device Act 2012.
• License Types: Importer, Distributor, and Authorized Representative.
• Purpose: Legal requirement to import and distribute medical devices in Malaysia.
• Regulator: Ministry of Health Malaysia.
• Scope: Pharmaceutical Wholesale License (PBKD, Health Supplement Distribution, Import of scheduled & non-scheduled products.
• Requirement: Ensures all medicinal and supplement products are registered, safe, and effective.
As an ISO 9001:2015 certified company, Revery upholds internationally recognized standards for quality management across every aspect of our operations. This certification reflects our commitment to consistent excellence, continuous improvement, and delivering reliable, high-quality products and services. It’s our promise that every experience with Revery meets the strictest benchmarks of professionalism, safety, and performance.
• Issued Under: Poison Act 1952.
• Purpose: Allows storage, handling, and sale of scheduled poisons, including prescription medicines.
• Mandatory For: Pharmacy and wholesale pharmaceutical operations.
• Requirement By: MDA.
• Purpose: Ensures proper handling, storage, transportation, and traceability of medical devices.
• Based On: ISO 13485 principles.
• Recognition: International standard for aesthetic medicine training.
• Holders: Aesthetic doctors with advanced certification in injectables, lasers, and skin treatments.
• Regulator: Ministry of Health Malaysia.
• Purpose: Legal requirement for doctors performing aesthetic medical procedures.
• Types: Type I: Non-invasive, Type II: Minimally invasive, Type III: Surgical aesthetic procedures.
• For: Doctors & Nurses.
• Purpose: Practical and theoretical training in aesthetic procedures recognized in Malaysia.
• Scope: Lasers, fillers, botulinum toxin, PRP, chemical peels.
• Regulator: MMC (Malaysian Medical Council) / Lembaga Farmasi / Nursing Board.
• Requirement: Annual CPD points to renew APC or practicing license.
• Importance: Keeps professionals updated on medical advancements and ethical practice.
• Issued By: SIRIM QAS International.
• Applies To: Selected medical devices and health-related equipment.
• Purpose: Confirms compliance with Malaysian Standards (MS), Allows use of the SIRIM Mark for quality assurance, Ensures conformity in safety, performance, and regulatory compliance.
