Palermo Street, 257 - Vila Santa Isabel 94480-775 Viamão – RS/ BrazilThe NSF Bioensaios laboratory began operations in 1990 giving services of chemical and biological analyzes for the environmental area, chemicals and foods. Currently conducts studies for registration and also analysis for quality control. Has a structure of more than 1200m 2, located in Viamao / RS and with the collaboration of more than 70 employees. Established primarily to perform ecotoxicity tests, was a pioneer in the sector. Over the years diversified its laboratories and expanded its field of expertise in the areas of contaminants in food and also safety assessment and characterization of chemicals such as pesticides, wood preservatives, oil dispersants, chemicals for water treatment and recently for drugs. Studies for characterizing and assessing the dangerousness of chemicals to humans and the environment. Analysis of contaminants in foods of vegetable and animal origin aiming to support food security and agribusiness. Analysis of environmental samples in accordance with the federal, state and municipal ordinances and resolutions. Support for the drug industry through the development and validation of analytical methods.
RS BrazilRemo Contract Research Organization (Remo CRO) offers full depth and breadth: preclinical, regulatory, and clinical service capabilities Consultation to strengthen your internal team Laboratory work on an array of preclinical cell and animal models Clinical trials support as needed through trial design, site selection, patient recruitment Sponsors get a customized services with a dedicated partner in Remo CRO Preclinical Service Line: Remo CRO Preclinical Services offers a full line of testing for efficacy and safety of your lead compound. We offer a wide range of experimental and disease models ranging from cell cultures to whole animal models and alternative species modelsWe incorporate bioinformatics with our Preclinical Development programs to identify ideal patient populations and minimize late-stage drug development failure. Our expert team is involved in every stage of your preclinical drug development from advising on experimental design to a comprehensive final report with raw data and full statistical analysis and interpretation. We offer Medical Writing (Clinical Research Protocols, Study Related Documents), Regulatory Document Assessment, Auditing & Compliance Overview, QC, Pharmacovigilance, Biostatistics. PRE-IND: Before initiating time-consuming non-clinical studies and establishing a clinical trial design, discuss plans with the FDA (and EMA) in a pre-IND meeting. Get FDA feedback on proposed IND studies and initial data. Remo CRO can arrange the pre-IND meeting, prepare the documentation package, and guide you to ask the right questions. IND: An IND application requests FDA authorization to administer an investigational drug or biologic to humans. It typically includes structure and composition of the candidate, manufacturing specifications, analytical evaluations, proposed safety studies, and the clinical study design. Remo CRO can ready your entire data and documentation package for an IND submission.
CB# 7070UNC Department of Otolaryngology focuses on research.