Success Story: Overcoming RFE to Secure NIW Approval for a Pharmaceutical Sciences Researcher
Client’s Testimonial:
"Thank you very much for all your help and support throughout my NIW case. I truly appreciate the effort from your team, especially during the RFE stage. I’m very happy that my I-140 has been approved.”
On May 7th, 2026, we received another EB-2 NIW (National Interest Waiver) approval for an Associate Researcher in the Field of Pharmaceutical Sciences (Approval Notice).
General Field: Pharmaceutical Sciences
Position at the Time of Case Filing: Associate Researcher
Country of Origin: China
State of Residence at the Time of Filing: Kansas
Approval Notice Date: May 7th, 2026
Processing Time: 11 months, 8 days (Premium Processing Requested)
Case Summary:
An associate researcher from China sought legal assistance from the North America Immigration Law Group (Chen Immigration Law Associates) for an NIW petition based on her work in pharmaceutical sciences. The client held a Ph.D. in pharmaceutical chemistry and had developed specialized expertise in mass spectrometry-based analytical methods, bioanalysis, drug metabolism and pharmacokinetics, and biopharmaceutical research.
The petition focused on her proposed endeavor to develop and apply advanced analytical methods for characterizing and quantifying small and large molecules in biopharmaceutical research. Our team emphasized how this work supports faster and more reliable drug development, improves the evaluation of therapeutic candidates, and advances innovation in pharmaceutical sciences.
Although USCIS issued a Request for Evidence (RFE) on December 16, 2025, the adjudicator confirmed that the proposed endeavor possessed both substantial merit and national importance. The remaining challenge was to further demonstrate that the client was well-positioned to advance her work. In response, our legal team prepared a detailed RFE rebuttal supported by updated and expanded evidence.
The response highlighted the client’s strong record of 10 peer-reviewed journal articles, 1 preprint, and 1 patent application, with publications appearing in respected venues. Her work had received 153 citations, including 107 independent citations, and several of her papers ranked among the top 10% and top 20% most-cited Pharmacology & Toxicology articles for their publication years.
We also documented her extensive peer review service, including at least 40 completed reviews for journals and conferences in pharmaceutical sciences. The petition emphasized that, due to its clear national importance, her research had been supported by funding from the U.S. National Institute of Allergy and Infectious Diseases, the U.S. Department of Defense, and the U.S. National Institute of General Medical Sciences.
Secured following a Premium Processing upgrade requested on October 15, 2025, this successful turnaround reflects NAILG’s careful presentation of a case that connected the client’s pharmaceutical sciences background, citation impact, peer review record, and future research plans to broader U.S. interests in drug development, therapeutic innovation, and biopharmaceutical competitiveness.

