Management Forum courses

...These changes have all been reflected through 100’s of quality conferences and seminars as we continue to deliver up-to-date and topical information...

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

...put compliance monitors in tablets, it cannot be long before auto-injectors and pen injectors use electronics to not only monitor compliance...

...on regulatory developments in pharmacovigilance in Europe, the USA, and Japan...

...population kinetics, biotechnology etc. The lecturers, who come from academia, industry and the regulatory agency, have many years’ experience in this area... Learn about: Drug Discovery...

...– from Drug Discovery to Product Launch and Beyond Understand the background of European Law – Regulations, Directives, etc. Discover where you can find...

...that any cosmetic products you already sell in the EU are legal Understand what is a cosmetic product, what makes it not a cosmetic and the ramifications...

...an unrivalled reputation in the industry. Topics cover all aspects of the Pharmaceutical drug development process and our portfolio is continually being...

...This conference will be of importance to all those involved in the Medical Device Industry in the following departments; Manufacturing, Research and Development...

...a regulatory role which involves post market surveillance, it will also be useful to clinical staff who have a desire to understand more about the vigilance...

...including detail about the specification itself and practical considerations for implementing the eCTD in your organisation. Suitable for: The course...

...Making best use of supplier documentation Understanding of terminology and the ‘busting’ of some myths Practical approach to documentation and document...

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

...backgrounds will find this event useful: Account Management Project Management Artwork/Origination Quality Assurance Business Development Quality Control...

...working in the health care, manufacturing and medical device markets. QA/RA Directors, Managers and personnel Consultants charged with creating or evaluating...

...standards Understand the Orange Guide Gain guidance from the UK MHRA Healthcare Regulations. WHO SHOULD ATTEND This training course is aimed...

...in particular, economic evaluation and the role it plays in determining access and coverage of new therapies. The objective of this course is to provide...

...industry in the following departments: Business Development, Regulatory Affairs, Registration, Quality Assurance, Marketing, Manufacturing, R&D and Technical Affairs...

...Bioequivalence ~ use of OIP guidelines Regulatory Review of Generic Approvals Device Characteristics Developing Inhaled Generic Products for the US Market SPEAKER PANEL...

...who are used to working with medicinal products but need to learn about clinical study requirements for medical devices. Anyone who is involved in conducting...