04/08/2026
FOR IMMEDIATE RELEASE
LMHRA Showcases Regulatory Progress At Global Drug Regulatory Conclave 2026 In India
Monrovia, August 2026– The Liberia Medicines & Health Products Regulatory Authority (LMHRA) represented Liberia at the Global Drug Regulatory Conclave (GDRC) 2026, held on July 30–31, 2026, at Bharat Mandapam in New Delhi, India.
The high-level international forum, jointly organized by India's Central Drugs Standard Control Organization (CDSCO) and the Pharmaceutical Export Promotion Council of India (PHARMEXCIL), brought together medicines regulatory authorities from more than 50 countries, alongside global pharmaceutical and healthcare stakeholders to advance regulatory cooperation and innovation.
Representing LMHRA, Dr. Matu K. Fayiah-Nyanti, Manager of the Post-Market Surveillance Unit, delivered a presentation titled: "Quality Without Borders: Shared Responsibility," highlighting Liberia's progress in strengthening medicines regulation through improved product registration, post-market surveillance, pharmacovigilance, laboratory oversight, quality assurance, and regulatory enforcement.
She emphasized LMHRA's collaboration with the Ministry of Health, law enforcement agencies, customs authorities, regional institutions, and international partners to combat counterfeit and substandard medical products while ensuring access to safe, effective, and quality-assured medicines. Dr. Fayiah-Nyanti also called for enhanced international regulatory cooperation and increased access to Indian Pharmacopoeia (IP) reference standards to strengthen Liberia's medicines quality testing capacity.
Following her return, Dr. Fayiah-Nyanti formally presented her GDRC Training Certificate to LMHRA Managing Director Hon. Dr. Luke L. Bawo and Deputy Managing Director Madam Patricia Qaye-Freeman. She expressed appreciation to the Authority for the opportunity and pledged to apply the knowledge acquired to further strengthen regulatory services and public health protection in Liberia.
The LMHRA leadership commended Dr. Fayiah-Nyanti for representing both the Authority and Liberia with distinction and encouraged her to share the knowledge and experience gained with colleagues. "This reflects LMHRA's continued commitment to institutional capacity building, professional development, and strengthening Liberia's medicines regulatory system," the leadership noted.
The Authority remains committed to ensuring that all medicines and health products available in Liberia meet the highest standards of quality, safety, and efficacy through innovation, collaboration, and international partnerships.
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Media Contact
Risk Communications & Public Relations Unit
Liberia Medicines & Health Products Regulatory Authority
(LMHRA)