It is very important that these compliance requirements are implemented based on the type of the product and the country where the products are being sold. These requirements are practiced to ensure the integrity of data and that correct steps are taken for public safety. GxP encompasses multiple compliance-related activities such as good laboratory practices (GLP), good document practices (GDP), good manufacturing practices (GMP), and good clinical practices (GCP). GxP compliance is an overarching term covering a broad range of regulations related to the life sciences industries, such as the fields of food and medical products. Proper management of your audit trail can lead to a streamlined process, accurate and instantaneous analytics of every step of the process, and a much easier long-term storage solution than paper records.ĭata integrity and GxP compliance are two very important terms for manufacturers and scientists who are trying to achieve the best for their customers, as well as their facilities. In the digital age of permanent and instantaneous recordkeeping, it is more important than ever to structure your business around the maintenance of good records within your FDA audit trail, or risk being fined, audited, or other potentially disastrous consequences. New means of data tracking are leading to higher standards of robust recordkeeping. New standards are evolving in the digital era with compliance in the laboratory.
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