Management Forum courses

...The programme will cover the regulatory requirements but will also share the interpretation of the regulation, guidance and legislation in these countries...

...mechanisms and formularies GERMAN REIMBURSEMENT SYSTEM Establish routes to market Understand current funding and reimbursement mechanisms Discuss...

...We are at the cutting edge of information exchange, organising over 250 conferences, seminars and residential schools every year. All of our events...

...and development departments, adverse reaction monitoring units, regulatory affairs and registration departments; pharmaceutical physicians and drug safety officers...

...Clinical Pharmacologist, Independent Consultant in Pharmaceutical Medicine Dr Rashmi Shah, Pharmaceutical Consultant and former Senior Clinical Assessor at the MHRA Don Walker... Learn about: Drug Discovery...

...in your area of business and our Seminars and Residential Schools provide an intimate, interactive environment in which to learn about the latest techniques and developments...

...to market cosmetics in the UK or throughout Europe Understand the Notification process If you have any queries, please contact Sarah Spanswick...

...and understanding of the rules governing the promotion of medicines in these different markets, with a particular focus on Europe. It will contain highly interactive workshops...

...Japan, Canada and Australia, this provides a unique insight into the performance of devices in the post production phase. Full compliance with the Vigilance...

...monitoring and reporting of adverse incidents. This meeting is appropriate for all those concerned with monitoring and managing the safety and performance...

...to the eCTD Considerations when selecting tools for the eCTD Process changes for the eCTD Practical experiences of submitting eCTDs...

...Explain how GEP concepts may be applied in the healthcare industry. Balance expenditure and activity against the associated risks and benefits of a defined scope of...

...to allow you to exchange experiences with other delegates. Suitable for: Anyone involved in pharmaceutical regulatory affairs in the Middle East Anyone...

...Design Your Security and Audit Trails Learn More About Bar-Coding Symbologies Take Away a Road Map to Outsourcing Clarify the Origination Guidelines...

...The course will provide valuable assistance and advice to all MDD regulated companies reviewing the status of their product range with respect to the new directive...

...RPs / QPs Directors Heads and Managers of: Wholesale Supply Chain Management Logistics and Logistics Systems Warehousing / Distribution QA / QC Planning...

...to best practice in health economics. It will help you understand how to integrate economic studies into the development process and communicate appropriately to their customers...

...product registration and labelling requirements in Asia Pacific markets BENEFITS IN ATTENDING Now that the European Medical Device market is well established...

...Dr Steve Nicholas, OINPD Specialist Consultant Dr. John Warren, Consultant (formerly with the MHRA) Dr. Jag Shur, Director, Nanopharm Ltd Martin Oliver...

...of the revised standard, as well as personnel new to medical device study management. The course will be particularly useful to clinical, regulatory...