Your biomedical company has scientific expertise and resources, and you are ready to take the next step - regulatory agency interaction to move your product to the clinic. Or, you may be contemplating licensing, partnering, or other M&A opportunities, and you want to hone your exit strategy and preparedness. 

Small companies commonly lack full-time staffing in the three functional domains needed for these next steps: Regulatory Affairs; Regulatory Operations; and Medical Writing. Outsourcing can fill these gaps, often needing diverse vendors over extended periods. While outsourcing is necessary in small biopharma to remain lean and nimble, finding reliable providers for these varied needs is challenging and time-consuming.

R&D Advisors has expertise and resources to assist with project-specific or organizational needs in all three functional areas. Our experience spans drugs, biologics, devices, and combination products, across many therapeutic areas.

Please explore this site and feel free to contact me to discuss your needs and goals. I look forward to hearing from you.