Regulates the traceability of products through a unique identification system, based on international guidelines. The purpose is to increase the effectiveness of activities related to post-market safety. To do this, aspects such as identification in the supply chain, the nomenclature of medical devices, the aforementioned system of unique identification of products, the registration of manufacturers, importers, etc. Are monitored. Each health system must have its own traceability system.
For example, in argentina they have the national drug traceability system, while in the united states this body is called the drug supply chain security act, better known as dscsa . Thus, depending on the territory in which we find ourselves, the legislation and the fax number list different processes involved in traceability may vary. As we have seen, traceability covers a wide range of processes that seek to guarantee the safety of medicines and medical devices. Surely you already know much better what the traceability of a medicine is !the first milestone in the history of the knowledge of dna dates back to the first half of
the 20th century and we owe it to the chemist rosalind franklin (and later, watson and crick) who demonstrated the double helix structure. Fifty years later, the second great discovery took place, when the first sequencing of the human genome was published in 2003 . The 10 years of research and the 3,000,000,000 dollars invested in the human genome project, allowed access to the "first book of life" ( grch30 ), with a total of 30,000 genes and about 3,120 million genetic instructions. This enormous discovery was the basis on which various tools in the field of genomics were developed. The main