MHRA GMP and GDP 2014 Symposium : Register Now...

9-12 DECEMBER 2014

London Novotel West, London

This not-to-be missed annual MHRA event will provide a unique platform for cross-collaboration and discussion between Industry and Regulators on the latest hot topics and regulatory updates related to Good Manufacturing Practice (GMP) and Good Distribution Practice (GDP):

• 09 December 2014 - GDP Symposium
• 10 December 2014 - GMP Symposium
• 11 December 2014 - GDP Symposium (repeat of 9 December 2014)
• 12 December 2014 - GMP Symposium (repeat of 10 December 2014)

Benefits of attending:

• Learn about the quality issues affecting your organisation.
• Develop increased awareness of MHRA expectations and changes.
• Recognise commonly seen GMP/GDP deficiencies and learn how to improve compliance in your organisation.
• Discover what your peers are doing through managed interactive workshops.
• Understand the impact of legislative changes on your business, including the Annex 15 and Annex 16 revisions.
• Learn more about the QP and RP roles.
• Meet the GMP/GDP Inspectorate teams and have the opportunity to ask questions on aspects affecting your organisation.
• Identify key quality critical areas in your own organisation.

Registration

Early bird tickets are available now! 

Visit event website at  http://www.mhragmdp.co.uk/ to book.

Who should attend?

All individuals from the pharmaceutical industry working in quality control; quality assurance; regulatory compliance and operations management within the manufacturing and distribution of medicines. These events will be of particular interest to Qualified Persons (QPs) and Responsible Persons (RPs). Good Distribution Practice (GDP) event will also be of interest to senior managers, supervisors and key staff members involved in warehousing and distribution activities.

Why attend?

• Improve the compliance of your organisation by understanding current issues being seen by the regulator and steps you can take to avoid these.
• Keep up to date with the many changes taking place in EU GMDP including Annex 15, Annex 16, FMD, RP gold standard and expectations with respect to data integrity.
• An opportunity to share concerns and learn knowledge from the MHRA and others working in the same business.
• The only forum to meet and share experiences with a large and diverse selection of QPs and RPs.