About Us
GLR Laboratories Pvt Ltd is a Biocompatibility service provider with laboratories based in India and consultation offices in the UK, USA, and Ireland. Our laboratory is OECD Good Laboratory Practice (GLP) and ISO 17025:2017 accredited. All in vitro and in vivo biological studies are conducted in our laboratories at Chennai, India, and chemical characterizations are conducted at our partner facility in Mumbai, India.
All safety assessments and other toxicology work are managed by our consultation offices in India, UK, USA, and Ireland.
Infrastructure
Facility and Resources
- 20,000 ft2 custom designed compact laboratory work space
- CPCSEA approved in vivo laboratory with 30 animal rooms
- Surgical theatre for implantation studies
- In vitro laboratory with several cell culture facilities
- Genetic Toxicology laboratory
- Pathology, Hematology and Clinical Biochemistry laboratories
- Separate unit for extract preparation, a key step in biocompatibility assessment
- We have analytical chemistry instrumentation (GC-MS, LC-MS, ICP-OES) at our partner laboratories
- Dedicated Test Item Control and Archival facilities are available
- The test facility is OECD GLP and ISO 17025:2017 accredited and has a separate Quality Assurance unit
Scientific Team
Our staff have a sound Scientific and Regulatory background and are professionals from the following fields:
- American board certified as well as UK/EU registered Toxicologists
- Medical professionals
- Veterinarians
- Pharmacologists
- Pathologists
- Biomedical engineers
- Biotechnologists
- Biochemists
- Regulatory professionals
- IT professionals
Leadership Team
Why GLR?
GLR offers pioneering support for all your outsourced toxicology needs backed by the highest scientific and service commitment.
GLR is headed by senior toxicologists, who have extensive experience, working in various International and Indian CROs, and with a wide range of clients.
At GLR, we always ensure comfort of our clients through the period of the study and thereafter.
High Quality Standards
At GLR, we strongly believe that all clients require high quality results that they can confidently depend on for their regulatory or product development needs. To ensure this GLR has implemented a Quality Assurance System that will fulfill all GLP and ISO 17025 requirements, as well as industry-tested good practices from other GxPs.
Cost Effectiveness
As a small CRO and located in India, GLR is in a position to offers cost effective solutions without compromising the quality or scientific integrity of the studies.
Network of Laboratories and Consultants
GLR has an extensive network of working partners in terms of various laboratories/consultants in India and abroad. This enables us to position ourselves as a One-Stop-Shop for Toxicology, by offering practically the widest range of toxicology or pharmacology studies for our clients.
Regulatory and Scientific Consultations
Scientific consultations are our major strength, which most of the other Asian CROs do not offer. Our experts have proven experience in moving lead candidates to IND and subsequent market approval. They can suggest you suitable research options enabling a quick turn-around of studies for regulatory submissions. To support our scientific needs we have an extensive network of academic and industrial scientists who work with us on a part-time basis.