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GLP (Good Laboratory Practice) is a quality system created specifically for non-clinical health and environmental safety studies. The aim is to ensure that the studies carried out are reproducible, traceable and at internationally acceptable standards.
A pharmaceutical product undergoes toxicologic and pharmacologic testing before it is placed on the market. The reliability and accuracy of these tests directly depend on GLP compliance.
1. Data Integrity and Reliability
GLP requires that experimental data is obtained, analyzed and reported accurately. Every step is documented and becomes auditable. This transparent structure is especially critical for regulatory authorities (EMA, FDA, etc.).
2. Protection of Human Health and the Environment
GLP aims not only at product safety, but also at the protection of workers and the environment in the experimental environment. Risks to laboratory personnel working with chemicals are minimized.
3. International Harmonization and Acceptability
For pharmaceutical companies operating worldwide, GLP means global validity. In order for a product to be approved in Europe or the USA, it must be supported by studies that comply with GLP requirements.
4. Audit Preparation and Corporate Reputation
A laboratory working within the framework of GLP rules provides an advantage in any audit process. Complete documentation and clear procedures minimize the risk of potential fines and reputational damage.
With the increasing awareness of quality in recent years, interest in GLP has been growing rapidly. Especially in innovative areas such as biotechnological medicines, vaccines, and personalized therapies, it has become a necessity for laboratory processes to be GLP compliant.
GLP is also becoming integrated with digital data systems. With software such as LIMS (Laboratory Information Management Systems), data tracking can be done more safely and effectively. GLP is an indispensable standard to ensure the safety of pharmaceutical products. GLP is of great importance in terms of data integrity, compliance with regulations and protection of human health.
Nanolab offers a reliable solution partner in pharmaceutical R&D processes with its infrastructure fully compliant with international GLP standards. Our headquarters laboratory in Istanbul provides a wide range of testing facilities for physical, chemical and in vitro analyses, while our Edirne branch is home to an advanced research center specially designed for in vivo animal experiments conducted within the framework of ethical rules. Thanks to these two strong locations, Nanolab offers a combination of global compliance and high quality in the pharmaceutical and biotechnology sectors.
Click here for our GLP Certificate.
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