Management Forum courses

...Approvals, Withdrawals etc Assess the Impact of the EU Clinical Trials Regulation Gain an Understanding of the Common Technical Document Discuss how... Learn about: IT Law, Directives etc, EU Law...

...should expect three comprehensive days of training. WHY YOU SHOULD ATTEND An Introduction to the Medical Device Directives ~ this course will help... Learn about: Medical training, Pharmaceutical manufacturing, Life Science...

...that should be applied during the collection of clinical evidence for both pre and post market studies. It will provide delegates with information on... Learn about: Quality Training, Medical training...

...Understand the Regulatory Framework Comply with the MEDDEV on Stand Alone Software Know the Principles to Bring a Medical Device Software Product to... Learn about: Usability training, Usability and resulting design documentation, Medical training...

...their leadership skills to a higher level as well as those new to or aspiring to a leadership / management role. This includes:- Team leaders Project leaders... Learn about: Skills and Training, Team Leader, Medical Devices...

...Finance Finance Training Administration Management... Learn about: Pharmaceutical Marketing, Life Science, Intellectual Property...

...MAA Parts IIIA & IIIB US FDA approach to HFS Studies User safety risk assessment in the EU Planning pre-clinical and clinical development Environmental... Learn about: US government, EU Regulations, Drug Development...

...WHO SHOULD ATTEND This three-day course will be of interest to all those in the pharmaceutical industry who prepare research reports and documentation... Learn about: Clinical Research, Medical training, Presentation Skills...

...attorneys in private practice Corporate patent attorneys and lawyers People working or training in intellectual property COURSE OVERVIEW This seminar combines... Learn about: Intellectual Property, Intellectual Property Law, European Law...

...Topics to be covered in this seminar Recent decisions from the EPO and the US impacting patents on software and computer technologies Procedures and pitfalls... Learn about: European Law, Life Science, Patent Protection...

...to help you keep up-to-date on the latest developments within Pharmaceutical and associated industry sectors. Management Forum's Intellectual Property... Learn about: IT Law, Life Science, Patent Claims...

...compliance and human factors associated with DPIs. These linked topics are creating a whole new area that requires better understanding during product... Learn about: Medical Devices, Intellectual Property, Pharmaceutical Marketing...

...Different Aspects of the Process for Obtaining the CE Mark for a Device Discover a Holistic Approach to Device Development and Marketing Participate... Learn about: Quality Training, Team Training, Medical training...

...With the underlying framework in mind, the approval and clearance processes for new and modified devices will be presented, including 510(k)... Learn about: Medical training, Pharmaceutical Regulations, Medical Devices...

...be of maximum benefit to those safety professionals who are working both in the Clinical and Post-Marketing Safety arena including QA for auditing... Learn about: Risk Management, IT risk...

...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: Intellectual Property, 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: Life Science, Medical Devices, Medical training...

...interest to all those who need to learn about successful marketing authorisation applications and regulatory compliance in key African regions... Learn about: Medical training, French Speaking, 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: Intellectual Property, Legal expertise, Medical Devices...

...It is essential therefore to have a number of SOPs, and for existing SOPs, to be reviewed and updated regularly. Otherwise this is likely to result... Learn about: Life Science, Confidence Training...