The company has been accredited with the International Quality Certifications and successfully implemented a well-documented Quality Management System which has been certified by ISO 13485:2016, ISO 9001:2015 and ICMED 9000. Our products are CE marked (EU Regulatory Compliant) from DNV GL PRESAFE AS. La-med is registered with Indian FDA and approvals of Drugs Department, QMS certificates has been received. Our products are registered in many more countries as per local regulation.

La-med export over 150 million devices to over 55 countries globally. Our brand is well recognized and respected in the markets we cover. La- med has local representatives in many countries.

La-med has a strong marketing base within the home country India, where we have a strong well trained and organized sales team covering the whole country. Over 300 SKU are being marketed in our own brand all over the country. Primaflon, IV flon, Primaneo, Link, Drippy, OncoGuard, etc are some of our popular brands.

La-med has a strong innovation team which focus on improvement of existing products and introduction of new products as per the market feedback and needs identified by our marketing team.

The company has plan to introduce many innovative products with underline principle of safety and simplicity to facilitate better patient care through innovation in line with our philosophy of Conscious caring.

Vision

Our Vision is to contribute to the improvement of the end consumer’s quality of life, through safe and reliable products that are manufactured with advanced technology, friendly towards people and the environment.

Mission

Our Mission is directly addressing the needs of our clients on a global level, through the constant improvement of our products and services, emphasizing especially the development of our human resources and corporate social responsibility.

Values

Our values shape the culture of our organization and define the character of our company. We live the core values through individual behaviors. They serve as the foundation for how we act and make decisions.

 

World Class Facilities

The “La-med” team has more than a decade of combined experience in the manufacturing, distribution and marketing of high-end single-use medical devices. Combined with the backing of strong professional and sophiscated manufacturing facilities, we are equipped to cater to the most demanding clients adhering to stringent deadlines.

Spread over a sprawling 75, 000 sq 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 the US- FDA & ISO guidelines, a controlled environment through HEPA filtration implementaon 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 molding in class 100,000 controlled environment; assembly, packaging and online printing in class 10,000 cleanroom; in-house sterilization facility, Physical, chemical and biological testing in a modern in-house laboratory. In compliance with European Council Directive 93/42/ EEC of 14 June 1993 concerning medical devices, as amended by 2007/47/EEC, ISO 14971:2012 Drugs and cosmetics act 1940 & Rules 1945 of India and Medical device rule 2017 ect.

We not only comply to international authorises, but utilize this as a base to build on, by implementing it.