Remo 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.