Mayuri is a Drug Product Development Scientist with 12+ years of experience in preformulation, formulation development, process scale-up, and technology transfer of oral solid, topical, semisolid, and sterile dosage forms of small molecules. She is highly skilled at enabled formulation technologies such as amorphous solid dispersions for improving exposures of poorly soluble compounds. As a Consultant at Syner-G BioPharma Group, she supports clients across pre-clinical to clinical stages, guiding CMC strategy, CRO/CMO selection, formulation design, and GMP manufacturing while ensuring regulatory compliance. She has contributed to multiple regulatory submissions (IMPD, IND) and is recognized for solving complex development challenges and driving programs to successful clinical/commercial outcomes.