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Agricultural biologicals may be global. Regulatory pathways aren’t

Bringing a biological crop protection product to market requires more than a strong technical dossier. Regulatory requirements can vary significantly across the US, Canada, EU and GB, influencing development plans, data requirements and time to market.

Sagentia Regulatory, formerly TSG Consulting, helps with:

  • Regulatory strategy and market access planning
  • Complex biological submissions, including microbial dossiers, secondary metabolite assessments and whole genome sequencing reviews
  • Product registrations, renewals and dossier development, including data gap assessments, literature reviews and regulatory submissions
Organic tomatoes representing Sagentia Regulatory's biologicals regulatory services

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Rolling green fields of crops under a blue, cloudy sky; distant patchwork farmland stretching representing Sagentia Regulatory's product authorisatons in Europe consultancy services

Product authorisations in Europe

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Clearing the path for biological product commercialization

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Infographic illustrating key phases in the acquisition and development of a biopesticide | Sagentia Regulatory

Key phases in the acquisition and development of a pesticide and/or biopesticide (EU)

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Infographic representing steps to plant protection active substance renewal and approval | Sagentia Regulatory

Steps to secure EU active substance approval and renewal

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Environmental sciences

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Cover of article: Navigating EFSA's revised birds and mammals guidance

Navigating EFSA’s revised birds and mammals guidance

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US and Canada regulatory services

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Global regulatory compliance

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