Regulatory Management

RIFCON offers comprehensive professional services for the registration of plant protection products (incl. biopesticides) and their active substances in the EU as well as non-EU countries. Our portfolio covers each section and phase of the complete registration process at both active substance and product level.

The challenges of the registration process are numerous and detailed requirements are constantly changing. These challenges are familiar to our experienced project managers and skilled specialists who devise cutting-edge state-of-the-art strategies to ensure successful registration.

Our project managers clarify the scope of the projects, develop registration strategies to meet the specific needs of our clients and coordinate the compilation of the required registration documents according to agreed timelines.

Our service quality is based on experience and ability

Our experts in product chemistry, analytical methods, toxicology, residues & metabolism, environmental fate & behaviour, ecotoxicology and efficacy monitor the planning and performance of studies, conduct the required risk assessments and prepare the entire dossier package for your intended registration.

The close collaboration between our various specialist teams, our clients and authorities as well as the continuous training of our staff enable us to address the latest regulatory requirements and evaluate the needed data package. Our strict quality management ensures high professional standards. As such, our years of experience combined with an excellent track record make RIFCON a partner you can rely on.

Our Services

Registration strategy

Development of strategies & solutions for active substance & product registration

Registration management

Taskforce management / Authority contact / Lead management with authority

Data analysis

Data gap analysis / CoC and GD compliance / Preliminary assessment / Cost estimation

Study monitoring

Lab communication / Quotation gathering / Monitoring services

Dossier compilation

Coordination, preparation & submission of dossiers

IUCLID

Dossier compilation in IUCLID format

Pre-submission

Coordination of pre-submission meetings

Caddy

Dossier compilation in CADDY format

Post-submission

Addressing of authority requests / Commenting tables

Classification and labelling

MSDS, Reg (EC) No 1272/2008

Literature surveys

Extensive data base researches

Information management and data compilation

AIR tracking / Research & compilation of regulatory relevant information / Compilation of GAP & label information, database development & maintenance

Management of changes

Source, composition & packaging material

Our Services

Registration strategy

Development of strategies & solutions for active substance & product registration

Registration management

Taskforce management / Authority contact / Lead managament with authority

Data analysis

Data gap analysis / CoC and GD compliance / Preliminary assessment / Cost estimation

Study monitoring

Data gap analysis / CoC and GD compliance / Preliminary assessment / Cost estimation

Dossier compilation

Coordination, preparation & submission of dossiers

Management of changes

Source, composition & packaging material

Pre-submission

Coordination of pre-submission meetings

Caddy

Dossier compilation in CADDY format

Literature surveys

Extensive data base researches

Information management and data compilation

AIR tracking / Research & compilation of regulatory relevant information / Compilation of GAP & label information, database development & maintenance

Post-submission

Addressing of authority requests / Commenting tables

Classification and labelling

MSDS, Reg (EC) No 1272/2008