MediPharm Labs Enters Landmark Commercial Agreement with Laboratório Teuto in Brazil

In This Article:

  • MediPharm Labs expands its Brazilian presence where the medical cannabis market is estimated to be worth $198 million in 2024, serving over 670,000 patients.1

  • Products include full-spectrum, GMP sublingual oral solutions with extensive pharmaceutical validation and characterization.

  • Teuto is one of Brazil's largest pharmaceutical manufacturers of both generic and branded medicines, with an extensive portfolio of oncologic specialty drugs, making it an ideal partner for MediPharm.

BARRIE, ON, Jan. 8, 2025 /CNW/ - MediPharm Labs Corp. (TSX: LABS) (OTCQX: MEDIF) ("MediPharm" or the "Company"), a leader in pharmaceutical-grade cannabis manufacturing, is proud to announce a commercial agreement with Laboratório Teuto ("Teuto"), a leading pharmaceutical manufacturer and marketer in Brazil. This partnership signifies a significant milestone as MediPharm expands its reach into one of the most tightly regulated medical cannabis markets globally.

MediPharm Labs Logo (CNW Group/MediPharm Labs Corp.)
MediPharm Labs Logo (CNW Group/MediPharm Labs Corp.)

ANVISA Product Approval Marks Commercial Milestone Achievement

ANVISA (Agência Nacional de Vigilância Sanitária) granted Teuto Sanitary Authorizations for two products manufactured by Medipharm. The approvals, published on December 30, 2024, mark the culmination of a rigorous process that underscores MediPharm's commitment to compliance, quality, and innovation in the global medical cannabis space. MediPharm and Teuto have been working closely together on the ANVISA approvals, which included pharmaceutical-level product filings, extensive quality control documentation, and responding to multiple requests for information over many months. Initial Shipments are expected to begin in the new year after applicable import and export permits from ANVISA and Health Canada are received.

Brazil's medical cannabis market is known for its stringent regulatory requirements, including:

  • ANVISA onsite GMP Inspections: Ensuring adherence to the highest pharmaceutical standards.

  • Comprehensive Product Dossier Submissions: Requiring a minimum of 12 months of stability testing and rigorous quality assurance.

  • Extended Product Approval Timelines: Reflecting Brazil's commitment to patient safety and product efficacy.

There are currently only 36 valid cannabis product authorizations issued by ANVISA under RDC 327/2019.2

MediPharm Labs is one of just a few North American companies with products to receive multiple sanitary authorizations for cannabis products while holding an ANVISA GMP licence. The Brazilian medical cannabis market is growing over 20% annually and is projected to exceed $260 million by 2026.3 Teuto can use its existing deep roots in Brazil and sales and marketing expertise to position itself as a leader in pharmaceutical cannabis.