Management Forum courses

...to register products in Europe and the regulatory activities that need to be complied with to keep products on the market. Pharmacovigilance and safety... Learn about: IT Law, EU Law, Directives etc...

...An Introduction to the Medical Device Directives ~ this course will help you gain a comprehensive understanding of the regulatory requirements... Learn about: Medical Devices, Medical training, Pharmaceutical manufacturing...

...European regulations for gathering clinical evidence and conducting medical device studies and help them to run studies in Europe and other countries... Learn about: Medical training, Quality Training...

...In addition, practical tips on how to streamline the development process, understand the regulatory requirements and how Notified Bodies review Technical Files will be covered... Learn about: Medical training, Usability and resulting design documentation, Software specification...

...designed specifically for the Pharmaceutical, Healthcare and Device industries, will be relevant for existing leaders and managers who wish to enhance... Learn about: Medical Devices, Team Leader, Skills and Training...

...principles, techniques and potential of biotechnology. WHY YOU SHOULD ATTEND Gain an introduction to the fundamental principles of Biotechnology... Learn about: Life Science, Pharmaceutical Marketing, Regulatory Compliance...

...and clinical development Environmental risk assessment phases I and II EU and US target animal safety Minor Use and Minor Species (MUMS) Writing and managing... Learn about: Animal Nutrition, Drug Development, Regulatory Compliance...

...of documents most frequently encountered in clinical research. Suitable for: This three-day course will be of interest to all those in the pharmaceutical... Learn about: Clinical Research, Enhancing Writing Skills, Medical training...

...defend claims according to European practice Achieve adequate protection while meeting official requirements Benefit from practical workshop exercises... Learn about: Claim Drafting, European Law, Medical Devices...

...WHY YOU SHOULD ATTEND Learn about development strategies impacting software patents Find out about the major developments in European patent... Learn about: Legal expertise, Life Science, Software development sourcing...

...We are at the cutting edge of information exchange, organising over 250 conferences, seminars and residential schools every year. All of our events... Learn about: Intellectual Property, Patent Claims, IT Law...

...Scientific research Medical marketing Marketing and Business development Key Annual Conference for Pharmaceutical and Medical Device Professionals in... Learn about: Medical Devices, Intellectual Property, Pharmaceutical Marketing...

...to the needs of other professionals, scientists, clinicians and regulatory and quality experts. This comprehensive course has been designed to map... Learn about: Quality Training, Team Training, Medical training...

...understanding of the underlying legal and regulatory requirements and the “general controls” applicable to all devices, including device classification... Learn about: Medical training, Medical Devices, Pharmaceutical Regulations...

...ensure you build and maintain a quality Pharmacovigilance department ready for any Pharmacovigilance inspection Participate in group workshop sessions... Learn about: IT risk, Risk Management...

...It will also help anyone thinking of studying for an MBA who would like an idea of what is involved. It is particularly beneficial to attend with a colleague... Learn about: Veterinary science, Intellectual Property, Medical Devices...

...that have been in the news recently. Your input will be requested prior to the course to decide what topics are included in the final agenda... Learn about: Medical Devices, Medical training, Legal expertise...

...Pharmaceutical Regulatory Affairs in Africa, including South Africa. Countries to be covered include Botswana, Ethiopia, Ghana, Kenya, Maghreb... Learn about: Medical training, French Speaking, Pharmaceutical Regulations...

...WHY YOU SHOULD ATTEND This meeting will give an introduction of the EC system for Variations with practical advice on the preparation and submission... Learn about: Medical training, Medical Devices, Legal expertise...

...SOPs incorporate appropriate regulatory requirements WHY YOU SHOULD ATTEND This SOP course has been specifically designed to hel you develop the skills... Learn about: Life Science, Confidence Training...