Singapore – TÜV SÜD PSB, a globally recognised quality and safety testing, inspection, certification and auditing organisation, is now officially listed as one of World Health Organisation (WHO) Prequalified Quality Control Laboratories of Pharmaceuticals. This qualification recognises that TÜV SÜD PSB’s laboratories are in compliance with WHO recommended standards governing Good Practices for National Pharmaceutical Control Laboratories (GPCL) and Good Manufacturing Practices (GMP) for the testing and analysis of pharmaceutical products.
The WHO Prequalification Programme aims to ensure that quality control laboratories meet necessary international standards for the analysis of pharmaceutical products. In order to achieve successful qualification, rigorous checks/ audits are performed by WHO’s team of inspectors and experts. TÜV SÜD PSB now joins the rank of 10 other national laboratories/ research institutes who have successfully achieved this status.
TÜV SÜD PSB is equipped with modern analytical testing equipments to help pharmaceutical companies, healthcare organisations, medical product distributors, and procurement agencies meet the necessary product quality and validation requirements for drugs and pharmaceutical products. With more than 30 years of experience in testing, TÜV SÜD PSB is able to provide a comprehensive range of pharmaceutical testing services covering chemical analysis and testing of pharmaceutical products and raw materials according to BP, USP, and EP methods, microbiological testing, preclinical testing services and environmental monitoring. TÜV SÜD PSB’s laboratories are also accredited to the requirements of ISO 17025 by the Singapore Laboratory Accreditation Scheme (SAC-SINGLAS).
For more information on the pharmaceutical testing services provided by TÜV SÜD PSB, please contact Dr Hou Xinping, Assistant Vice President at telephone no : +65 9637 3132 or email : Xinping.hou@tuv-sud-psb.sg
Jane Lim, Manager, Public Relations
T +65 6885 1527 F +65 6776 8670