01/06/2026
STRENGTHENING REGULATION IN VETERINARY MEDICINES AND ALLIED SUBSTANCES FOR ANIMAL AND PUBLIC HEALTH
From 26th–29th May 2026, the Zambia Medicines Regulatory Authority (ZAMRA) conducted a Stakeholders Sensitisation Training on Regulatory Requirements for Veterinary Medicines and Allied Substances, bringing together key players in the veterinary medicines sector.
Speaking at the beginning of the training, Acting Director-General Mr. Lyoko Nyambe highlighted that the rapid growth of Zambia’s livestock sector and companion animal care presents both opportunity and regulatory responsibility.
"Effective regulation protects your reputation, safeguards animal welfare, prevents the threat of antimicrobial resistance, and ensures that our farmers and pet owners can trust the products they use."
Over the four days, participants engaged in discussions on critical regulatory requirements under the Medicines and Allied Substances Act, including:
- Registration of veterinary products before market entry
- Good distribution practices to maintain product integrity
- Labelling and advertising standards
- Adverse event reporting
- Marketing Authorisation procedures and timelines
- Post-Marketing Surveillance (PMS)
- Requirements for clinical trials
- Import and export permit requirements
- Navigation of the Integrated Regulatory Information Management System (IRIMS)
- Requirements for food supplements, feed additives, and premixes
The training also provided an important platform for stakeholder engagement, helping to build a robust and practical regulatory system while promoting compliance and creating a level playing field for all industry players.
At the end of the training, Doctor Daniel Ndambasiya thanked the stakeholders for their input and reiterated ZAMRA's commitment to combating non-compliance, protecting animal and public health, as well promoting food safety.