GLP certification is a recognition that your laboratory follows standardized protocols in conducting non-clinical research. It ensures the reliability, consistency, and integrity of data submitted to regulatory authorities such as the FDA, OECD, and EMA. Unlike ISO certifications, GLP is not issued by a single body but is verified through inspections from designated national authorities.
GLP consulting helps labs implement SOPs, train personnel, validate instruments, and maintain detailed records in line with international GLP guidelines.
Laboratories operating without GLP risk rejection of their study results in regulatory submissions. For businesses involved in drug development, food safety, cosmetics, and chemical testing, GLP is a non-negotiable requirement. It also builds a foundation for higher certifications such as GxP, ISO 17025, or FDA 21 CFR Part 11.
Choosing GLP not only supports regulatory approvals but ensures data produced in your lab meets scientific integrity and reproducibility standards.
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