This meeting has been designed to give practical advice and guidance on how to successfully develop market approval in the EU. The programme will take participants through a step-by-step approach to the process and will also provide key guidance on how to maintain MA once achieved.
17-18 Apr 2018
Also on: 16 Oct 2018
Two day meeting on Regulation Update on Animal Feed and Feed Additives in the EU, USA and China, annual conference now in its 6th successful year.
Advanced Veterinary Pharmacovigilance – the purpose of this course is to provide a comprehensive, yet practical assessment of the main requirements to ensure a compliant reporting Company.
21-22 Mar 2018
Also on: 2 Oct 2018
A practical five day In-house course Working through Veterinary Drug Development in the EU and the USA
An essential course for ensuring compliance with Regulatory Requirements which will be of particular relevance for Pharmacovigilance, Regulatory Affairs, Clinical Research/Operations, GMP, QA and Document Management Functions
6 Dec 2017
Also on: 28 Jun 2018
A basic In-house training course for those working on drug safety in the EU. This course has been designed to provide basic training and a good introduction to those concerned with veterinary pharmacovigilance.
2-3 May 2018
Also on: 7 Nov 2018
This comprehensive two day course will introduce you to the core concepts of what makes an excellent leader – in the context of the pharmaceutical industry – and how to apply the different skills of leading your staff and team to maximise results
21-22 Jun 2018
Also on: 26 Nov 2018
Learn how to prepare a Request for Proposal (RFP), evaluate and select the right CRO and establish procedures for vendor oversight for R & D projects you need to outsource.
20-21 Mar 2018
Also on: 4 Oct 2018
This seminar will take many aspects of animal health and veterinary research and development through a typical clinical trial and pay attention to compliance with GCP as outlined in the two guidelines on safety and efficacy produced by FEDESA and CVMP.
9-10 May 2018
Also on: 31 Oct 2018
This course will take participants through all of the necessary steps to obtain marketing authorisation for a feed additive in the European Union.
23-24 May 2018
Understand the licensing of veterinary vaccines by USDA and CFIA, understand the phased submission process for vaccine licensing, and learn the format and content specifications for the required dossier components.
19 Apr 2018
Also on: 18 Oct 2018
Presentations will cover the regulatory framework, pharmaceutical, toxicological and pharmacological data, safety risk assessments, pre-clinical and clinical data, Detailed and Critical Summaries and regulatory submissions
28-29 Nov 2017
Also on: 25 Apr 2018