Hospital Design Engineering team with international exposure and 2000+ labour workforce ready to execute massive projects.
With our extensive research on complex health systems, healthcare management, and start-up operations, we know what it takes to capture the market and unlock profits. We know how to create a sustainable and prosperous healthcare model that can thrive in today’s highly competitive business environment.
We have a good understanding of patients’ behaviour and psyche and know where precisely to hit to take your healthcare business to the ‘next level.’ We know how you can acquire as well as retain the patients. We have the strategies to improve your patients’ engagement, which is critical to ensure business turn around in the current times.
Our methods, strategies approach and focus on long-term goals keep the short-term milestones into consideration, with our extensive research and development on healthcare. We know why many healthcare companies face stagnancy or decline after gaining significant success.
We have in-depth know-how, expertise, and tactical skills to aid your business growth with the right decisions and guidance.At LIFA HEALTH, with its strong knowledge of the micro and macroeconomic environment’s essentials to successfully run a healthcare business.
We are distinguished in creating successful business models and brand positioning with a focus on profitability, brand building, and long-term value creation. We have a profound understanding of the deep-rooted challenges that businesses have to face in the healthcare arena.
FDA 510K is a premarket submission made to FDA to demonstrate that the device to be marketed is as safe and effective, that is, substantially equivalent, to a legally marketed device (section 513(i)(1)(A) FD&C Act). ... Legally marketed also means that the predicate cannot be one that violates the FD&C Act.
C.E. marking is a certification mark that indicates conformity with health, safety, and environmental protection standards for products sold within the European Economic Area (EEA). ... The C.E. marking is the manufacturer’s declaration that the product meets E.U. standards for health, safety and environmental protection.
SITRA - The South India Textile Research Association (SITRA), one of the four approved laboratories in the country to test coveralls, masks, and fabric used to make these, is getting 100 to 150 samples a day for certification. Some companies make reusable coveralls with woven or knitted fabric with coating.
ISO 13485 Certified” means an organization has implemented an ISO 13485 Quality Management System and has successfully met all of the requirements in ISO 13485.ISO 13485 evaluates whether your Quality Management System is appropriate and effective while emphasizing the safety and efficacy of medical devices.
2015 certification (for Environmental Management Systems): ISO 14001:2015 specifies the requirements for an environmental management system that an organization can use to enhance its environmental performance. ISO 14001:2015 can be used in whole or in part to improve environmental management systematically.
Over 12,000 ASTM standards are used all over the world to improve product quality, enhance health and safety, strengthen market access and trade, and to let customers know they can count on products. ASTM serves many industries, such as metals, construction, petroleum, consumer products, and more.
Medical Gloves for Single Use. Part 2 Requirements and Testing for Physical Properties. This standard includes tests for glove dimensions and physical strength. Physical properties’ requirements depend on the glove classification (surgical/examination) and material (Latex, Nitrile, Vinyl, Polythene).
A TUV certification means a sampling of the product has been tested for safety and met the German Equipment and Product Safety Act’s minimum requirements. If you’ve ever looked for outdoor lighting, you’ve probably looked for a U.L. wet location safety rating.
