Management Forum courses

...of support staff wishing to gain a greater understanding of Regulatory Affairs in the Pharmaceutical Industry. It is also suitable for those who interface... Learn about: EU Law, IT Law, Directives etc...

...all those who intend to place a medical device on the market and anyone who requires an overview of the medical device sector... Learn about: Medical training, Pharmaceutical manufacturing, Life Science...

...data is a key aspect of continued safety and performance considerations once the device is on the market. This course will cover the full range of activities... Learn about: Quality Training, Medical training...

...Process /Manufacturing Engineering Staff Document Control / User Manual Writers R&D Software Engineering Team Members and GUI Designers Someone from admin... Learn about: Medical training, Usability training, Risk Management...

...of the Pharmaceutical industry – and how to apply the different skills of leading your staff or team to maximise results. You will become competent and... Learn about: Team Leader, Skills and Training, Medical Devices...

...Training Administration Management COURSE OVERVIEW Biotechnology for the Non-Biotechnologist, ideal for non-Scientists and Scientists needing to understand the basic theory... Learn about: Intellectual Property, Pharmaceutical Marketing, Regulatory Compliance...

...ATTEND Gain a comprehensive understanding of the processes for the EU and USA, including: EU and US regulatory frameworks, strategies and procedures MRLs Parts A... Learn about: Drug Development, Animal Nutrition, US government...

...Participants will learn both the theoretical and practical aspects of writing for regulatory authorities as well as the sensible use of international guidelines... Learn about: Presentation Skills, Enhancing Writing Skills, Medical training...

...Benefit from practical workshop exercises, led by two highly experienced trainers Trainee patent attorneys – preparing short or long term to qualify Patent... Learn about: European Law, Intellectual Property Law, Medical Devices...

...the United States and Europe on the scope of available patent protection Learn tactics for US practice and the latest US strategies in dealing with obviousness... Learn about: Legal expertise, Patent Protection, European Law...

...approach in order to decide upon inventive step. It looks easy, but when applied, it should be applied correctly. This is not just a formal matter... Learn about: Patent Claims, Life Science, IT Law...

...DPI Market THREE REASONS TO ATTEND Key annual gathering for pharmaceutical and medical device professionals in the DPI market Keep abreast of what’s happening in formulation... Learn about: Pharmaceutical Marketing, Intellectual Property, Medical Devices...

...Workshops and Learn from Other People’s Experiences Understand how Other Professionals Affect the Process for Bringing a Device to Market Network with... Learn about: Medical training, Team Training, Quality Training...

...IDE, PMA, HDE and De Novo applications. Application contents, review processes, timelines, and key guidance documents will be discussed for each major type of submission... Learn about: US Regulations, Medical Devices, Medical training...

...in group workshop sessions and discuss how to apply the legislation to ensure compliance, especially to satisfy regulatory inspection This course would... Learn about: IT risk, Risk Management...

...skills for more senior levels beyond more technical skills. It will also help anyone thinking of studying for an MBA who would like an idea of what is involved... Learn about: Veterinary science, Life Science, Medical Devices...

...with the topic selection based on areas of pharmacovigilance where inspection findings commonly occur. Delegates will also be offered some ‘hot topics’... Learn about: Intellectual Property, Medical Devices, Life Science...

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

...An introduction to the EC system for Variations The Current Variations Regulations of the European Commission and procedures in practice Review of latest... Learn about: Pharmaceutical Management, Intellectual Property, Legal expertise...

...It is therefore essential that they are well written and easy to use by the end users. If SOPs are not followed correctly, the validity of data generated is compromised... Learn about: Life Science, Confidence Training...