Regulatory Support - Biologicals
Registration of biologicals with a scientific strategy and regulatory vision
Registering biologics requires a different approach
The registration of biological products follows a different regulatory logic from conventional agrochemicals. Companies that apply the same approach face unexpected requirements and significant delays.
Evaluating the safety and specificity of microorganisms requires specific expertise in microbiology, ecotoxicology and regulation, a rare combination to find in a single consultancy.
With Law 15.070/2024 and Joint Ordinance SDA/MAPAP - IBAMA - ANVISA 01/2023 speeding up processes, companies that aren't prepared are missing out on a window of competitive opportunity.
How SmartTox solves
Detailed services
Safety and Biological Specificity:
Evaluation of the safety profile of the microorganism or biological control agent, including the tests required by Joint Ordinance SDA/MAPA - IBAMA - ANVISA 01/2023 and Environmental Risk Assessment:
Environmental Risk Assessment:
Analysis of the environmental impact of the biological product, considering specificity of action, persistence in the environment and effects on non-target organisms. Meeting IBAMA's requirements on a scientific basis.
Evaluation of Agronomic Efficiency:
Analysis of the experimental field protocol, with the entity accredited by MAPA for field tests, in accordance with Normative Instruction 36/2009, with updates to Normative Instruction 42/2011/SDA/MAPA.
Persistence and non-target organisms:
Studies and evaluations on the persistence of the biological agent in the environment and its potential effects on auxiliary fauna and flora, demonstrating the environmental safety profile required by the authorities.