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Animal Health

14 courses in this category:

17-18 Apr 2018
EUR 1959.00
GBP 1399.00
USD 2182.00

Also held on:
16 Oct 2018

A Practical Approach to Veterinary Vaccine Development and Registration in the EU

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.

Full details

7-8 Dec 2017
EUR 1959.00
GBP 1399.00
USD 2182.00

A Regulatory Update on Animal Feed and Feed Additives in the EU, USA and China

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.

Full details

21-22 Mar 2018
EUR 1959.00
GBP 1399.00
USD 2182.00

Also held on:
2 Oct 2018

Advanced Veterinary Pharmacovigilance

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.

Full details

4-8 Jun 2018
EUR 4199.00
GBP 2999.00
USD 4678.00

Animal Health Summer School - Working Through Veterinary Drug Development in the EU and USA

A practical five day course Working through Veterinary Drug Development in the EU and the USA

Full details

6 Dec 2017
EUR 979.00
GBP 699.00
USD 1090.00

Also held on:
28 Jun 2018

How to Write Effective SOPs

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

Full details

7 Dec 2017
EUR 979.00
GBP 699.00
USD 1090.00

Also held on:
29 Jun 2018

Improving Processes and CAPA (Corrective and Preventative Action)

This meeting will cover CAPA methodology and documentation, diagnosing process improvement, developing options for process improvement and CAPA and planning and implementation in practice of improvements and CAPA

Full details

2-3 May 2018
EUR 1959.00
GBP 1399.00
USD 2182.00

Also held on:
7 Nov 2018

Introduction to Veterinary Pharmacovigilance

A basic 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.

Full details

20-21 Mar 2018
EUR 2099.00
GBP 1499.00
USD 2339.00

Also held on:
4 Oct 2018

Managing Vendor/CRO/CMO Oversight in the Pharma Industry

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.

Full details

9-10 May 2018
EUR 1959.00
GBP 1399.00
USD 2154.00

Also held on:
31 Oct 2018

Practical Implementation of GCP in Veterinary Field Studies

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.

Full details

16-17 May 2018
EUR 1959.00
GBP 1399.00
USD 2182.00

Registration of Animal Feed Additives in the EU

This course will take participants through all of the necessary steps to obtain marketing authorisation for a feed additive in the European Union.

Full details

Registration of Veterinary Vaccines in the USA and Canada

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.

Full details

28-29 Nov 2017
EUR 1959.00
GBP 1399.00
USD 2182.00

Also held on:
25 Apr 2018

Veterinary Pharmaceutical Submissions in the EU

Veterinary Pharmaceutical Submissions in the EU. Chaired by Dr Julian Braidwood, Consultant to the Animal Feed

Full details

Developing Medicines for Companion Animals in the EU

This course has been designed to demonstrate how pharmaceutical, pharmacological, toxicological, pharmacological, safety risk assessments, clinical development, and regulatory submissions. An important part of the course will be devoted to working on case studies in the workshop sessions.

Full details

Introduction to the Development and Licensing of Veterinary Novel Biotherapeutics in the EU

Discover how to develop veterinary pharmaceuticals and vaccines, its regulatory landscape and how you might apply these principles to novel biotherapeutics.

Full details