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Doseology Engages McKinney Regulatory Science Advisors to Advance Innovative Oral Pouch Product Development through Science and Regulatory Expertise

Doseology Engages McKinney Regulatory Science Advisors to Advance Innovative Oral Pouch Product Development through Science and Regulatory Expertise

KELOWNA, BC, Jan. 12, 2026 /PRNewswire/ — Doseology Sciences Inc. (CSE: MOOD) (PINK: DOSEF) (FSE: VU70) (“Doseology” or the “Company”) a leader in biotechnology-driven consumer products, today announced a strategic partnership with McKinney Regulatory Science Advisors (“McKinney“), a premier FDA regulatory consulting firm specializing in nicotine and reduced-risk consumer products, to spearhead its regulatory submission strategy and solidify its commitment to scientific leadership in the oral pouch technology space.

Doseology Sciences Inc. Logo
Doseology Sciences Inc. Logo

This collaboration marks a pivotal advancement for Doseology, transitioning the Company towards regulatory execution and commercial readiness. McKinney’s comprehensive guidance will encompass formulation strategy, data generation, Pre-market Tobacco Product Application (“PMTA“) preparation, and post-market compliance. The aim is to position Doseology as a frontrunner in delivering differentiated, IP and/or trade secret protected oral pouch products to regulated markets with confidence.

“Doseology is committed to leading with science and innovation in the oral pouch category. Engaging McKinney, a leader in regulatory science, ensures that our product development is not only innovative but also strategically aligned with regulatory expectations,” said Tim Corkum, President & COO of Doseology. “This partnership underscores our dedication to building a defensible, regulatory-ready platform that prioritizes dose consistency and consumer safety.”

“At McKinney Regulatory Science Advisors, we value working with organizations that apply a rigorous, science-based approach to product development and evaluation. Doseology’s team has demonstrated a strong understanding of the role of regulatory science in identifying, characterizing, and managing product risks. We look forward to a collaborative partnership that will support the advancement of Doseology’s product portfolio,” said Dr. Willie McKinney, CEO of McKinney Regulatory Science Advisors.

Key Highlights of the Partnership:

  • Accelerated Regulatory Pathway: McKinney’s expertise is expected to expedite Doseology’s navigation of FDA requirements, with the objective of streamlining development timelines and reducing regulatory uncertainty.

  • Enhanced Product Design & IP Protection: The collaboration is expected to strengthen Doseology’s intellectual property by aligning formulation and testing strategies with regulatory standards, ensuring dose consistency, delivery performance, and stability.

  • Comprehensive PMTA Readiness: McKinney will provide structured preparation for PMTA submissions, covering both nicotine and innovative nicotine-analogue formulations.

  • Integrated R&D and Manufacturing: McKinney will integrate its regulatory roadmap into Doseology’s R&D program and manufacturing validation plans, ensuring formulation objectives, analytical testing, and quality systems align with regulatory expectations from the outset.

  • Commitment to Consumer Safety: This partnership underscores Doseology’s commitment to developing safe, effective, and transparently supported products, with McKinney’s counsel helping prioritize the right studies and documentation.

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