About Us
GLR Laboratories Pvt Ltd is Biocompatibility service provider with laboratories based in India and consultations offices in UK, USA and Ireland. Our laboratory is OECD Good Laboratory Practice (GLP) and ISO17025 accredited. All in vitro and in vivo biological studies are conducted in our laboratories in 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 facility
- Genetic toxicology Laboratory
- Pathology, hematology and clinical biochemistry laboratories
- Separate unit for extract preparation, a key step in biocompatibility assessment
- We have analytical chemistry instrumentations (GC-MS, LC-MS, ICP-OES) at our partner laboratories.
- The test facility is OECD GLP and ISO17025 accredited and has a separate quality assurance system, Test item control and Archives.
Scientific Team
Our staff have strong Scientific and Regulatory Background and are 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 excellent scientific and service commitments.
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 comfortably depend on for their regulatory or product development needs. To ensure this GLR has implemented the Quality Assurance System that will fulfill all GLP and ISO17025 requirements, as well as some 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
Even though we are a small CRO, we have 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 any 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 for 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 extensive network of academic and industrial scientists who work with us on a part-time basis.