Events

8th February 2012

The course will include all the major features of the Directive including, amongst others, product classification, conformity assessment routes and Technical Files including the Essential Requirements. The prime focus of this course will be on the Medical Device Directive, but will of course include reference to the IVD and AIMD directives.

9th February 2012

NIHR is keen to increase the volume and impact of research in surgery and will be holding a national workshop on surgery research at the Royal College of Surgeons of England, London on Thursday 9 February 2012.

9th February 2012

This meeting will provide a technological showcase highlighting the latest research in Dental imaging and materials from academia and industry for patient benefit.

15th February 2012

The 11th edition of the leading European conference and exhibition dedicated to innovation in packaging and drug delivery technologies for the pharmaceutical, biopharma and healthcare industry, will take place on 15–16 February 2012, in Paris.

16th February 2012

On Thursday 16th February, High Edge Consulting, in conjunction with Isotron, will run an intensive half-day course covering all the critical areas of design, development, production and quality control of sterile medical devices.

20th February 2012

Faced with diminishing resource and budget, Leaders within the NHS are having their management and leadership skills stretched to the limits.nThis course will help delegates to understand the complexities of change and lead in such a way that their staff are assured that the best possible course of action has been selected. It will also help the leaders themselves fully understand their role in all situations, including those in which they themselves do not ‘have the answer’, and the impact that their actions and behaviour will have on those around them.

7th March 2012

The aim of this unique short course is to provide a detailed insight into the scientific information generated through pre-clinical studies and review its potential application in later phases of the clinical evaluation process.

7th March 2012

This practical, workshop based course with case studies has been designed to provide delegates with the skill (including tools and techniques) and knowledge required to understand, interpret and apply ISO 14971 as well as the ability to integrate risk management into their existing organisation and Quality Management Systems.

13th March 2012

The course is designed to help regulatory professionals understand the fundamentals of the clinical trial process, such that they then have a suitable working framework from which to develop specific interrogation of problems and the development of solutions, when dealing with clinical trial issues in relation to product development and registration strategy.

13th March 2012

Welcome to Procurex National 2012, the UK’s leading FREE to attend two-day event for personnel engaged within the public procurement process.

19th March 2012

EEN are proposing an outward Trade Mission to Osnabruck, Germany in March 2012.

22nd March 2012

At A New Approach to Mental Health our expert speakers will explore the government's vision and discuss how the mental health strategy can be implemented to best ensure outcomes are successful.

26th March 2012

Once again we’re bringing you the must-attend forum for drug and diagnostic developers to build new personalised medicine partnerships and to give you a comprehensive understanding of how you can turn biomarker research into successful patient stratification.

18th April 2012

This course covers how to prepare for and how to receive a Regulatory Audit from a European Notified Body. It will provide vital information to both established companies and companies new to the medical device industry.

2nd May 2012

The EBME seminar is a commercially-independent educational event bringing together healthcare professionals that are responsible for the management of medical equipment. These medical equipment healthcare professionals are involved in areas such as procurement, maintenance, user training, and managing inventories.

9th May 2012

This practical and interactive course introduces delegates to auditing ISO 13485 and how it is integrated with the Medical Devices Directive and other regulations.

23rd May 2012

UBM Canon, the organisers of MEDTEC UK 2011, Midlands Design & Manufacturing, Mtec and 3C, would like to thank all visitors and exhibitors for making the event a terrific success! Attendance was up 33% compared to last year.

12th June 2012

The course is designed to provide students with an understanding of the skills required to control regulatory affairs departments and to achieve worldwide compliance and approvals. This will include a clear appreciation of organisational, product and portfolio management and the politics of regulation (influencing and lobbying).

26th June 2012

You are a technology supplier looking for a medical device design and manufacturing exhibition. You want an event that puts you directly in front of your target audience. One that centers on one of the world's fastest developing economies. MD&M Brazil is that exhibition and conference.

11th September 2012

The course will define the terminology and explain the concepts of vigilance, post-market surveillance and risk management, their practical applications and integration into the lifecycle of a medical device.

25th September 2012

The exhibition will cover all areas of the medical plastics supply chain – including design and prototyping, materials, clean room machinery (extrusion and injectionnmoulding), process control and sensing, mould making and temperature control, end of line / assembly, regulation and contract manufacturing.

26th September 2012

MEDTEC Italy will feature opportunities for educational development, both through the concurrent conference programme and within the exhibition. As the event draws closer, these pages will outline the events.