Regulatory Affairs

Check of completeness and data gap analysis, strategic advice and recommendations

Study management and monitoring of relevant GLP studies for physical and chemical properties, analytical methods, residues, environmental fate & behaviour as well as ecotoxicology

Dossier preparation and compilation for EU approval of as well as renewal of approval of active substances

Preparation of the zonal core dossiers and national addenda for product registration in the EU (dRR, MRL applications, LEX) for dossier sections on identity, physical and chemical properties, analytical methods, residues, environmental fate and ecotoxicology

Tier 1 and higher tier pollinator risk assessment and MRL setting in honey

Continuous support of national registrations mainly in EU member states but also in other countries around the globe

Bridging statements for demonstration of comparability of product formulations

Pre- and post-submission support

Literature searches and reviews (Regulatory Science)

We provide full registration support for active substances and plant protection products in the EU. We have scientific experts for identity, physical and chemical properties, analytical methods, metabolism and residues, environmental fate, ecotoxicology, toxicology and human exposure.

Our experts have detailed knowledge of the data requirements for the registration and re-registration as specified in current EU legislation, country-specific regulations and current guidance documents.

Why we have the expertise

This expertise is augmented by a deep reservoir of in-house specialist knowledge provided by senior staff members, which can be mobilised to handle complex authority requests or other non-standard situations that may arise during the registration.

Contact our expert

Dr. Heino Christl

heino.christl(at)tier3.de

Phone: +49 (0) 2171 55 997 14

Dr. Henning Immink

henning.immink(at)tier3.de

Phone: +49 (0) 2171 55 997 54

Regulatory Affairs​

Check of completeness and data gap analysis, strategic advice and recommendations​

Study management and monitoring of relevant GLP studies for physical and chemical properties, analytical methods, residues, environmental fate & behaviour as well as ecotoxicology​

Dossier preparation and compilation for EU approval of as well as renewal of approval of active substances​

Preparation of the zonal core dossiers and national addenda for product registration in the EU (dRR, MRL applications, LEX) for dossier sections on identity, physical and chemical properties, analytical methods, residues, environmental fate and ecotoxicology​

Tier 1 and higher tier pollinator risk assessment and MRL setting in honey​

Continuous support of national registrations mainly in EU member states but also in other countries around the globe ​

Bridging statements for demonstration of comparability of product formulations​

Pre- and post-submission support​

Literature searches and reviews (Regulatory Science)​