Clinical Research
Clinical research involves studies and trials to evaluate the safety and effectiveness of medical treatments, drugs, or devices. It typically includes phases from Phase I, II, III, and IV trials. Researchers work with human participants to collect data, which helps guide medical practices and regulatory approvals.
Biocompatibility and Toxicology Analysis Medical Devices
Biocompatibility and toxicology analysis for medical devices ensures that a device is safe for use in the human body. Biocompatibility testing evaluates how materials interact with tissues, cells, and bodily fluids to avoid harmful effects. Toxicology analysis assesses potential risks such as chemical leaching or long-term toxicity.
Ethics Commitee Registration Consultancy for Institutions and hospitals (ICMR-DHR and CDSCO Registration)
Ethics Committee Registration Consultancy helps institutions and hospitals navigate the process of registering their ethics committees with regulatory bodies like ICMR-DHR and CDSCO. The consultancy ensures compliance with ethical guidelines for conducting clinical research involving human participants.