European Union And USA Veterinary Drug Development Online Training Course, June 21-25, 2021 – PRNewswire

DUBLIN, June 16, 2021 /PRNewswire/ — The “Working Through Veterinary Drug Development in the EU (European Union) and USA Training Course” conference has been added to’s offering.

This intensive five-day course provides a thorough understanding of how to develop a veterinary medicine in the EU and USA.

The development of veterinary medicine is complex, time-consuming and expensive. It requires teamwork from individuals with different scientific training and a wide range of skills.

Everyone involved must be aware of the main stages in the development programme and be able to relate his or her responsibilities to the expertise and needs of the scientists and commercial members of the team.

Furthermore, different approaches taken by the regulatory authorities in the EU and the USA mean that a comprehensive development programme must be designed in order for the product to be commercialised in both regions.

The event has been designed to demonstrate how pharmaceutical, pharmacological, toxicological and clinical investigations and regulatory management are brought together in the development programme. It will take participants through all the stages in the development of a veterinary medicinal product for which marketing authorisation is sought in the EU and the USA.

Presentations will cover pharmaceutical and process development, toxicological, pharmacological, residues and environmental studies, safety risk assessments, clinical development, regulatory and marketing input and project management.

Gain a comprehensive understanding of the processes for the EU and USA, including:

EU and US regulatory frameworks, strategies and procedures n MRLs Parts A & B; MAA Parts IIIA & IIIB US FDA approach to HFS studies User safety risk assessment in the EU Planning pre-clinical and clinical development Environmental risk assessment Phases I and II n EU and US target animal safety Minor use and minor species (MUMS) Writing and managing regulatory submissions Who Should Attend:

This course has been designed for anyone who has limited experience in only one of the disciplines in veterinary medicine development, such as pharmaceutical or analytical development, clinical trials, regulatory affairs or quality assurance. Anyone learning the role of project manager, as well as more experienced personnel seeking to review special problems encountered in product development, will benefit from the comprehensive programme delivered by experienced professionals.

Previous delegates who have benefited from this course include clinical scientists, pharmaceutical scientists, marketing managers and personnel from regulatory affairs, R&D and development.

Key Topics Covered:

Day 1 09:00 – 15:00 UK/London

EU regulatory framework for regulation of veterinary medicines

What is the EU? EU legal framework for regulation of veterinary medicines Legal base of procedures and data requirements US regulatory framework for regulation of veterinary drugs

Current governing laws and regulations Federal agency jurisdictions EU and USA: differences and similarities

INAD and NAD in the USA Phased submission in USA vs marketing authorisation application in EU EU MRLs vs US HFS section EU renewal, variations, extensions vs US supplements EU certificate of suitability and EDMFs vs US DMFs Different requirements for user safety and environmental risk assessments The global development programmes

Requirements for EU Requirements for the USA Achieving a global development programme USA regulatory strategies and procedures

Applications for NCEs and supplements Generic drug applications EU regulatory strategies and procedures

Full and abbreviated applications Generic applications Centralised procedure Decentralised, MRP and national procedures Day 2 09:00 – 15:15 UK/London

MRLs Part A safety and MAA Part IIIA

The toxicological data requirements Determining the NOEL and ADI USA FDA approach to HFS studies

Toxicology studies Margins of safety MRLs Part B residues and MAA Part IIIB

‘Hot’ and ‘cold’ residue studies How to determine maximum residue limits Analytical methods for residues Determining the withdrawal period FDA evaluation of consumer safety

Human food technical safety section Residue issues Workshop – session 1

Day 3 09:00 – 14:45 UK/London

Environmental risk assessment Phases I and II

Critical evaluation of your data package Phase I assessment Refining risk assessment Phase II assessment Tiers A and B What to do if risk assessment gives cause for concern User safety risk assessment in the EU

Reviewing toxicology studies Setting the scenario Risk assessment and management Pharmacokinetics and bioequivalence

ADME studies Bioequivalence Workshop – session 2

Day 4 09:00 – 14:45 UK/London

EU and US clinical development

Dose selection Field studies VICH guidelines Claim-driven approach in the US Protocol review and concurrence with CVM Value of VICH guidance EU and US target animal safety

Pivotal target animal safety studies Filed safety studies New VICH guideline on TAS Minor use and minor species (MUMS)

MUMS approaches in EU and USA What are minor uses? What are minor species? Approaches to preparation of clinical data Workshop – session 3

Day 5 09:00 – 14:45 UK/London

Workshop – presentations

Pharmaceutical development and the CMC package

Characterising the active substance Formulation development Analytical development and setting specifications Process scale-up and validation Stability studies and shelf life Managing the USA regulatory submission

Systems of review at CVM Team interaction Company and regulator interactions Writing and managing the EU regulatory submission

Writing the marketing authorisation application Summary of product characteristics and labelling Working with writers on detailed and critical summaries in the EU Pre-submission advice and oral hearings For more information about this conference visit

Media Contact:

Research and Markets

Laura Wood, Senior Manager

[email protected] 

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SOURCE Research and Markets

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