La-med Healthcare Pvt. Ltd.
our infrastructure…
Spread over a sprawling 52, 000 sq ft with the scope for further expansion, our flagship unit is equipped to deliver close to 150 million finished devices annually.

With clean rooms meeting Class 10,000 standards designed as per US-FDA & ISO guidelines, a controlled environment through HEPA filtration implementation and compliance with all relevant national and global standards like strict hygiene standards of our own.

Six Sigma processes controls and TQM measures have been built into our processes rather than being externally implemented.

The manufacturing involves product design; injection moulding in class 100,000 controlled environment; assembly, packaging and online printing in class 10,000 clean room; sterilization; physical, chemical and biological testing in amodern in-house laboratory. In compliance with European Council Directive 93/42/EEC of 14 June 1993 concerning medical devices, as ammended by 2007/47/EEC, ISO 13485: 2003, EN ISO 14971: 2012 Drugs and cosmetic act 1940& rules 1945 of India etc. We not only comply international authorities, but utilize this as a base to build on, by implementing.
research & development
With in-house research and development for all our products and processes, we are also working on the development of special purpose machines and processes to optimize production and product quality.

Our intellectual capital in designs and teams of experienced staff constantly improve on the existing designs using latest 3D, CADCAM technology as well as through extensive investments in trials. Value addition to existing designs is a strong area of focus in our R&D cell.

Staying in constant touch with our end-users helps us to identify their needs. Our organised response system feeds directly into the R&D department, which makes a conscious effort to pre-empt their needs and expectations.

Conscious Caring” dictates all aspects of our performance from R&D to product usage.
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