We provide solutions that bring safety to the health field.
The principles of Good Laboratory Practice (GLP) define a set of rules and criteria for a quality system related to the organizational process and the conditions under which non-clinical environmental health and safety studies are planned, performed, monitored, recorded, reported, and archived.
Good laboratory practice applies to all non-clinical health and environmental safety studies as required by regulatory authorities for the approval or licensing of pharmaceuticals, pesticides, food and feed additives, cosmetics, veterinary drugs, and similar products, and for the regulation of industrial chemicals.
Its purpose is to ensure the quality, reproducibility, and integrity of data generated for regulatory purposes so that the data can be recognized internationally without the need to reproduce studies.
Oqotech provides GLP services guaranteeing the quality, reproducibility and integrity of the data generated for regulatory purposes so that the data can be recognized internationally.
Do you need more information about the requirements your company must meet regarding the regulations in force in the sector?
Oqotech's team has over 10 years of experience in the pharmaceutical, biotechnology and food industry. We guarantee that the organization complies with legislation. Leave your details and we will contact you to offer you more detailed advice.