Turning innovation into market-ready results

That depends on where you are in your journey. Many startups begin with proof-of-concept trials, but if you're considering commercialisation, you'll need GEP-compliant field trials. These trials meet regulatory standards and can be used in future registration dossiers, helping you avoid costly re-testing.

As early as possible. Many startups focus on performance and leave regulatory planning until it's too late, only to discover that their trial data can't be used for approval. By involving regulatory experts early, you can design trials that serve both technical validation and regulatory compliance.

GEP (Good Experimental Practice) is a quality standard required for efficacy trials of plant protection products in the EU. GEP trials follow strict protocols so that the data can be used in product registration. If your trials aren’t GEP-compliant, they likely won’t be accepted by regulatory authorities.

Yes. Agrolab Consulting has deep expertise in the regulatory pathways for biostimulants and biologicals, including EU North Zone requirements. We help you assess whether your product needs registration, and guide you through the most efficient approval route.

Costs vary based on your product type, target crops, and trial design. What we do offer is smart planning, we help you avoid duplicate trials by ensuring your first efforts support both technical and regulatory goals. That means fewer surprises and better use of your budget.

To receive a customized quote or discuss your specific needs, we encourage you to reach out to us for a non-binding consultation.

Absolutely. Whether you need help designing your trial, executing it in the field, interpreting drone or lab data, or navigating regulatory requirements, we’re used to working closely with startup teams. You’ll get one point of contact and a clear roadmap.