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: EU Law, IT Law, Directives etc...

...expects Better under Conformity Assessment Procedures, Classification, Medical Device legislation Comply with Manufacturing Responsibilities Consider... Learn about: Life Science, Medical Devices, Pharmaceutical manufacturing...

...and the emphasis on high quality, appropriate clinical evidence has grown substantially in the last few years. Clinical evidence is key to bringing a device... Learn about: Medical training, Quality Training...

...as the implications of the new draft Usability Standard. Practical advice on how to validate your system design will also be addressed. BENEFITS OF ATTENDING... Learn about: Usability and resulting design documentation, Usability training, Risk Management...

...leadership techniques which you will then go on to use on a daily basis when you return to the workplace, enabling you to perform at a higher level... Learn about: Skills and Training, Team Leader, Medical Devices...

...Biotechnology for the Non-Biotechnologist, ideal for non-Scientists and Scientists needing to understand the basic theory, principles, techniques and potential of biotechnology... Learn about: Pharmaceutical Marketing, Regulatory Compliance, Intellectual Property...

...development Clinical trials Regulatory affairs Quality assurance Anyone learning the role of project manager Experienced personnel seeking to review special... Learn about: US government, Animal Nutrition, Animal Care...

...intended for regulatory authorities. Although the focus of the seminar is on clinical research documentation, many of the principles will also apply to other types of reports... Learn about: Enhancing Writing Skills, Presentation Skills, Medical training...

...one day of claim drafting fundamentals with a further day of focused workshops. Attendees have the choice of either a mechanical or chemical workshop... Learn about: Intellectual Property Law, Medical Devices, European Law...

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

...approach in order to decide upon inventive step. It looks easy, but when applied, it should be applied correctly. The purpose of this seminar is to teach... Learn about: Intellectual Property, Patent Claims, Life Science...

...success story in improving inhaled drug delivery. However, we now have to tackle the technical and regulatory issues with ‘generic’ inhalers and their approval... Learn about: Pharmaceutical Marketing, Medical Devices, Intellectual Property...

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

...This seminar will provide a solid foundation in the approval and clearance processes for medical devices in the United States. Participants will gain... Learn about: Medical training, US Regulations, Pharmaceutical Regulations...

...KEY TOPICS TO BE COVERED Training for Drug Safety Reporting Duties, Audits and Expectations Risk Based Inspections The DDPS retirement and the New PV Master... Learn about: IT risk, Risk Management...

...Medical Device / Animal Health Industries wishing to develop their business management skills for more senior levels and beyond more technical skills... Learn about: Life Science, Veterinary science, Pharmaceutical Research...

...work in pharmacovigilance or an associated function. In particular it will look at the progress with the ‘new’ EU legislation, how it is being interpreted... 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 Science, Pharmaceutical Regulations, French Speaking...

...Variations The Current Variations Regulations of the European Commission and procedures in practice Review of latest requirements Biologicals and Biotech... Learn about: Legal expertise, Medical Devices, Pharmaceutical Management...

...Carrying out effective SOP training Ensure your SOPs incorporate appropriate regulatory requirements WHY YOU SHOULD ATTEND This SOP course has been specifically... Learn about: Confidence Training, Life Science...