WELCOME T0 BIOCOMPATIBILITY AND TOXICOLOGY TESTING AT GLR
GLR Laboratories Pvt Ltd is a Good Laboratory Practice (GLP) and ISO/IEC 17025:2005 accredited contract research provider specializing in toxicology and biocompatibility (ISO10993) of medical devices. It was founded in 2009 in India as a result of collaboration between Indian and UK scientists. The laboratories and the head office are located in Chennai, India and two overseas business offices in Cambridge, UK and Pennsylvania, USA.
We offer cost-effective and high-quality biocompatibility solutions for CE marking and regulatory submissions. Our reports are readily accepted by FDA and notified bodies. We are committed to scientific and service excellence, so that our clients can bring their devices quicker to market.
We also offer individualized services to clients in nonclinical safety testing of pharmaceuticals, chemicals and other products. In addition to General and Genetic Toxicology, our niche area of expertise is in-vitro Toxicology, Investigative Toxicology, Consultations and 3rd Party Study Monitoring.
GLR offers standard toxicology studies to fulfill regulatory requirements.
We also undertake other non-standard and investi- gative toxicology studies.
We have over 15 years experience in working directly with the Pharma, Biopharma, Medical devices and Cosmetics Industries.
We provide insight and advice on product development. We also undertake other non-standard and investigative toxicology studies.
GLR is conducting a Free One-day refresher/CPD course on medical device biocompatibility (ISO 10993), including recent update to ISO10993, Part 1, in Washington DC (6 April 2018) and Newark (9 April 2018). Please contact us for details.