GLP laboratory is mainly a specification formulated for the safety evaluation experiments of medicines, pesticides, food additives, cosmetics, veterinary drugs, etc. Regulatory documents formulated for a series of management of laboratory experimental research from planning, experimentation, supervision, recording to experimental reports, involving all aspects of laboratory work. The main purpose of formulating GLP laboratories is to strictly control all aspects of chemical safety evaluation tests, that is, to strictly control various subjective and objective factors that may affect the accuracy of experimental results, reduce test errors, and ensure the authenticity of experimental results.
According to the relevant regulations of the European Union REACH regulations that came into effect on June 1, 2008, all chemicals entering the EU market must be registered with the relevant departments within the specified time based on the safety evaluation data issued by the GLP laboratory before they can be sold in Europe. market sale.
Wangbo has a GLP laboratory in Australia with a complete lineup of technical teams and equipment to provide customers with the most professional and high-quality cell preclinical/clinical trial services
- Cell and animal experiment design, analysis and detection, bridging human clinical trials
- Planning of laboratories and cell operation units that meet EU standards for human experimentation(Cell Processing Unit, CPU)
- Set laboratory testing and safety standards for stem cell/immune cell therapy for various diseases(QC/QA)
- Advanced high-end cell and analysis testing laboratory
- Possess the ability to apply for cell storage banks of international standards(AABB)