Plexus Preclinical Services

Plexus supports their clients with wide knowledge in providing consulting services in the field of the nonclinical program for NCE development, including dose-response assessment, pharmacokinetics, regulatory toxicology, mechanistic toxicology, descriptive toxicology, in silico computational toxicology (QSAR) & GLP to the industries like pharmaceuticals, biotechnology (biosimilar & vaccine), herbal, cosmetic and medical device companies. Additionally, to support the conduct of various Non-Clinical studies in rodents and non-rodents, we have collaborations with wide number of CROs / academia which helps the client to ease the process of product development. PPS experts including European Registered Toxicologists (ERT), offer solutions to complex drug development, toxicological and regulatory issues related to Pre-Clinical development through their technical and regulatory knowledge gained with decades of research experience in various industries & CROs. Because of the experience, knowledge and dedication of PPS, most renowned research partners and business owners trust Plexus Pre-Clinical Services as a preferred research partner for their drug discovery and development services. PPS guides you through every process step, from creating a development strategy to your product being approved and regulated. Our services 1. Non-clinical development strategy for NCE/NPD/NBE/NDDS 2. Toxicological evaluation for various products 3. Medical Device Evaluation 4. Toxicology Risk Assessment (TRA) 5. GLP test facility setup / Facility upgradation 6. Trainings - Different modules of GLP / GDP / GCLP / Toxicology 7. Quality Assurance 8. Histopathology support 9. Regulatory service and support 10. Animal breeding setup / upgradation