About Us
Trademark and Companies
Imada, in response to the protection of trademarks and patents of each product, the establishment of this comprehensive limited company began in the 1950s with more than 70 years of history to date. Products are marketed around the world with the trust and love from foreign people, young to elderly, and they are advised to use safely as home and travel medicine.
Subordinate Agencies
Under our subordinate agencies, including Luen Wah (HK) Medicine Limited. , Imada Luen Wah World Limited, Imada Luen Wah Medicine (S) Pte Limited and multiple subsidiaries. Imada owns the development of its business, with product manufacture, license processing, management agents, patent and trademark protection, quality control and marketing to ensure credibility at its highest level.
Objective
Good Manufacturing Practice (GMP) is a quality assurance system widely used in the pharmaceutical manufacturing industry around the world. GMP ensures that pharmaceutical manufacturers can continuously and stably manufacture high-quality pharmaceuticals to meet the requirements of safety and quality standards through hardware and software guidelines for raw materials, plant, equipment, sanitation, personnel training and quality management. Imada has since adopted with these standard specifications for each of the production process, which must comply with the requirements of the scope of its regulatory standards, including sanitation, factory facilities, production control, quality control, staff training, document management and file records, etc. ,in order to provide highest quality products to the general public as the goal. From sourcing of raw materials , production to packaging which are all with a prudent and careful operation code of procedure. Luen Wah (HK) Medicine Limited to be sure to achieve the company’s promises: Safety, Efficacy and Highest Quality.
Quality Assurance
1. Select
Perform research, data analysis and carefully evaluate to define its reliability, practicality, and safety standards.
2. Source
Survey for potential resources and quality assessments, complete integrated plants and ensure the highest quality of raw materials through chemical testing.
3. Standardization
Require specific important marks in each production process, strictly standardization development and professional production methods to ensure product consistency and effectiveness.
4. Structure
Establish the structural integrity of each production process, and to strengthen research of each program.
5. Safety
According to existing research results, do standard safety evaluation for drug testing, and other safety testing against chemical toxins, heavy metals and pesticides.
6. Proofs
Implement and comply with GMP guidelines for production quality management standards, meets with regulatory requirements to ensure product quality, and requires further IMADA product development and research projects when needed.