Hindustan Syringes & Medical Devices Ltd.

HMD has multiple fully-integrated plants spread over four sites in the city of Faridabad, Haryana, India. These plants are designed to manufacture the entire range of HMD products, thus enabling minimal changeovers for variables and quick deliveries. Fascinating as it is, the total installed capacity of the plant has been set up with a capital investment of over $80 Million USD and enhanced for a production capacity of more than 4.5 Billion units per annum of disposables. Apart from these three plants, HMD has recently set up a newly built integrated plant in 2019 spread over 5 Acres of land at IMT Industrial Area. With the help of their newest plant, HMD would be able to gear up their production of Surgical Blades & Scalpels to over 150 Million Units. HMD is targeting to meet 50 percent of the world's growing demand for superior quality blades & scalpels. Apart from the IMT plant, HMD also set up another plant in 2014, a state of the art facility spread over an area of 6.5 acres of land. This new plant promises an estimated production capacity of 350 Million Syringes per annum ,36 Million I.V.Cannula per annum and 70 million Pen Needles. These plants are also equipped with state-of-art design and engineering facilities for developing new products and innovative variants of existing products, such as I.V.Cannulas, Nonreusable (AD) Syringes, and Blood Collection Tubes. All HMD Plants run 24×7, 6 days a week with high-speed assembly and packing lines assisted by online digital vision inspection systems to ensure consistent quality and thorough checking of all products. As pioneers in manufacturing Medical Devices for a globally demanding market, HMD showcases their technical prowess through the meticulous use of state-of-the-art technology. For instance, HMD uses Japanese Technology to manufacture Needles of all kinds, British technology for manufacturing Surgical Blades & AD Syringes, Italian for manufacturing Scalp Vein and Taiwanese technology for Sterilisation process. Public welfare has always been a mandate for HMD. Thus, the aim is to manufacture products that render optimum benefit to the patients and doctors and at the same time make the world a better place to live in.

QUALITY POLICY

The management of HMD affirms that it is the policy of the company to produce medical devices conforming to the relevant product standard specifications adopted by the company. It is the policy of the company to achieve internationally praiseworthy standardized quality with the help of the most appropriate mass production technology harnessed through a dedicated production team in a harmonious industrial atmosphere as per the requirements of ISO 9001, ISO 13485, ICMED 13485, European Medical Device Directive, Medical Device Regulations (Canada) and any other applicable regulation. And then offer it for the benefit of the patient and doctor at a price any other local manufacturer will find it difficult to meet, for similar performance specification.It is the policy of the company to keep on striving for continual improvement in Quality Management System effectiveness over and above the minimum stipulations laid down by the relevant product standard specifications adopted by the company. It is the policy of the company that in case of a customer complaint or defects being reported, all endeavors would be made by the top management to promptly attend to the complaint and compensate the loss of the customer by arranging the free replacement of the rejected goods or by some mutually satisfactory agreement.

QUALITY ASSURANCE

HMD is a market leader in the field of Healthcare by adhering to all the international standards and internal norms for producing medical consumables using highly automated technology. When it comes to quality assurance, HMD conforms to ISO:13485, ICMED: 13485, MDSAP and ISO:9001 standards, encompassing a comprehensive and exhaustive series of visual, physical, chemical, and microbiological tests & inspection at various stages in the production cycle. The quality assurance process begins with constant surveillance of raw materials and its suppliers, intensive in-process control of all manufactured components and sub-assemblies to the final inspection and testing of the finished products. Apart from this, 6 Sigma is practiced throughout the organization to ensure consistency, quality, and minimal chances of defectives reaching the consumer. The ongoing analysis of data gathered through customer feedback & internal processes, followed by required corrective and/or preventive action, ensures for continuous improvement in our product and further enhances for deeper customer satisfaction.