Our role is to provide comprehensive support to manufacturers and importers in meeting the strict regulatory requirements under Act 852. We assist clients throughout the full product registration process, ensuring every submission aligns with current industry legislation and compliance standards. As part of our service, we prepare complete documentation sets required for SIRIM MS2716 approval, including all technical, safety, and quality-related materials. This ensures that each product meets national specifications before being released to the Malaysian market.
In addition, we develop and compile the full technical file needed for submissions to the Ministry of Health (MOH). This includes coordinating test reports, product specifications, declarations, and all supporting documents necessary for regulatory assessment. Our aim is to streamline the approval journey by guiding clients through each procedural step with accuracy and clarity.
By engaging our consultancy, manufacturers and importers significantly reduce the risks of rejection, delays, and non-compliance issues. We help prevent costly setbacks by ensuring all requirements are met efficiently and professionally. Ultimately, our expertise allows clients to navigate the regulatory landscape with confidence, enabling faster market entry and long-term compliance under Malaysia’s evolving vape industry regulations.