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After sales service support is the most important part of any business, the good technology should be backed with good service support. LC Process has highly experienced team of professionals with 20+ years of hands on experience in various chromatography technique, more then 10+ years of thorough experience in service and maintenance of Prep HPCL and DAC Column. Team members are trained in Japan, USA, France, Germany and various platform in India and abroad. The best training and upgradation of knowledge is on the field, while repairing any Prep HLPC system or packing a DAC Column. The precious inputs form the end-user, the technical requirements of the scientist add to the knowledge of engineer. The good efficient service should be backed with stock of spare parts, LC Process maintain stock of spares and consumables to reduce the downtime. We are reachable 24 x 7 x 365 Days. We value your time, we respect you work and we understand that timely communication and prompt intelligent service make difference, adds value. LC Process Prep HPLC System and DAC Column comes with quality and excellent service support.
LC Process manufacture finest piece of equipment, accurate in performance, precise in reproducibility, rugged in operation, chemically compatible, mechanically strong and safe Process HPLC System and DAC Column, with most appropriate specifications, regular upgrades, one of most user friendly software, easy to learn, simply to operate, complying 21 CFR Part 11 guidelines. LC Process believe that development cannot be permanent and improvisation cannot be constant, both are a continuous process and we at LC Process follow the same policy, continuous improvisation, which is based on the rich precious feedback. The improvisation and modification on existing installation, the customization of new specification for any specific requirement, all is positively possible at LC Process. Mechanical customization, modification or Software, we do it all. LC Process understand your requirement and build the machine to suit your application and purification method. There are many interesting, young features, that our rep can share with a visit your site.
ASME helps the global engineering community develop solutions to real world challenges. Founded in 1880 as the American Society of Mechanical Engineers, ASME is a not-for-profit professional organization that enables collaboration, knowledge sharing and skill development across all engineering disciplines, while promoting the vital role of the engineer in society. ASME codes and standards, publications, conferences, continuing education and professional development programs provide a foundation for advancing technical knowledge and a safer world. ( Source : asem.org )
BIS is the National Standard Body of India established under the BIS Act 2016 for the harmonious development of the activities of standardization, marking and quality certification of goods and for matters connected therewith or incidental thereto. BIS has been providing traceable and tangible benefits to the national economy in a number of ways – providing safe reliable quality goods; minimizing health hazards to consumers; promoting exports and imports substitute; control over proliferation of varieties etc. through standardization, certification and testing. ( Source : Bureau of Indian Standards. )
ASTM International is a globally recognized leader in the development and delivery of voluntary consensus standards. ASTM Standards are used around the world to improve product quality, enhance health and safety, strengthen market access and trade, and build consumer confidence. ASTM serve a broad range of industries, When new industries — like nanotechnology, additive manufacturing and industrial biotechnology — look to advance the growth of cutting-edge technologies through standardization, many of them come to ASTM International. The American Society for Testing and Materials was formed in 1898, founded by Charles B. Dudley, Ph.D., a chemist with the Pennsylvania Railroad. In 2001, ASTM changed our name to ASTM International. ( For more information refer the Source : astm.org )
CE Marking to a product, a manufacturer declares that the product meets all the legal requirements for CE marking and can be sold throughout the EEA. This also applies to products made in other countries that are sold in the EEA.
ATEX, Directive 99/92/EC also known as 'ATEX 137' or ATEX Workplace Directive are guidelines on requirements for improving the health and safety protection of workers potentially at risk from explosive atmospheres. Detailed guideline are explained on EU website. Directive 99/92/EC also known as 'ATEX 137'.
GMP regulations require a quality approach to manufacturing, enabling companies to minimize or eliminate instances of contamination, mixups, and errors. GMP regulations address issues including record keeping, personnel qualifications, sanitation, cleanliness, equipment verification, process validation, and complaint handling. Most GMP requirements are very general and open-ended, allowing each manufacturer to decide individually how to best implement the necessary controls. This provides much flexibility, but also requires that the manufacturer interpret the requirements in a manner which makes sense for each individual business. GMP is also sometimes referred to as "cGMP". The "c" stands for "current," reminding manufacturers that they must employ technologies and systems which are up-to-date in order to comply with the regulation.
21 CFR Part 11 :This guidance is intended to describe the Food and Drug Administration's (FDA's) current thinking regarding the scope and application of part 11 of Title 21 of the Code of Federal Regulations; Electronic Records; Electronic Signatures, 21 CFR Part 11. ( Reference : US-FDA ).
GLP, Good Laboratory Practice is defined in the OECD Principles as “a quality system concerned with the organisational process and the conditions under which non-clinical health and environmental safety studies are planned, performed, monitored, recorded, archived and reported.” The purpose of the Principles of Good Laboratory Practice is to promote the development of quality test data and provide a tool to ensure a sound approach to the management of laboratory studies, including conduct, reporting and archiving. ( For further information refer source : who.int )
For Purity, Its Chromatography,
For Chromatography, Its LC Process !