Management Forum courses

...provides an introduction to Pharmaceutical Regulatory Affairs and the basics of drug development and has been designed specifically for those working in a support staff... Learn about: IT Law, EU Law, Directives etc...

...Classification, Medical Device legislation Comply with Manufacturing Responsibilities Consider the requirements for Quality Systems Plan your Clinical Evaluations... Learn about: Medical Devices, Pharmaceutical manufacturing, Medical training...

...Authorities and obtain other necessary approvals Understand the key aspects of pre and post market study setup, management, monitoring and close down Discuss... Learn about: Quality Training, Medical training...

...will be explained for Medical Device Software products. Software specification, risk management, architectures, usability and resulting design documentation will be discussed... Learn about: Medical training, Usability and resulting design documentation, Usability training...

...This comprehensive two day course will introduce you to the core concepts of what makes an excellent leader – in the context of the Pharmaceutical industry... Learn about: Medical Devices, Team Leader, Skills and Training...

...and why and how they must be protected WHO SHOULD ATTEND Quality Assurance Regulatory Affairs Legal and IP Business Development Sales and Marketing Engineering... Learn about: Life Science, 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: Regulatory Compliance, EU Regulations, Animal Care...

...standards and useful writing tips. Many illustrative examples will be used, drawn from the seminar leaders’ wide experience of the pharmaceutical industry... Learn about: Enhancing Writing Skills, Presentation Skills, Clinical Research...

...PLEASE NOTE Attendees will benefit from bringing a copy of the European Patent Convention with them. WHY YOU SHOULD ATTEND Gain a good understanding... Learn about: Intellectual Property Law, Intellectual Property, 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: US Law, Intellectual Property, Legal expertise...

...researched by our experienced course directors and designed to help you make informed decisions and remain up to date with 'need to know' business information... Learn about: Intellectual Property, IT Law, Patent Claims...

...when developing a DPI to gain regulatory approval. How to develop a generic DPI: from scratch to market Designing drugs for inhalation – achieving solutions... Learn about: Intellectual Property, Pharmaceutical Marketing, Medical Devices...

...It will commence with a general introduction as to what devices are and how they are developed, and continue with lectures, workshops and case studies... 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: US Regulations, Medical Devices, Pharmaceutical Regulations...

...(2nd Revision requirements) Implications for Safety Reporting in Global Clinical Trials Risk/Benefit Determinations Risk Management Plans WHY YOU SHOULD... Learn about: Risk Management, IT risk...

...Working in the highly competitive Bio / Pharmaceutical Industry, with ever-increasing change and pressure, is probably one of the most challenging managerial... Learn about: Pharmaceutical Research, Life Science, Intellectual Property...

...such as regulatory, clinical, medical information or quality. It will help you understand what they are asking for from you and why, enabling you to... Learn about: Medical training, Life Science, Intellectual Property...

...with Regulatory Submission Strategy Recent developments in South Africa Harmonisation and Co-operation Initiatives in Africa This seminar will be of particular... Learn about: Pharmaceutical Regulations, Medical Science, Medical training...

...requirements Biologicals and Biotech Pharmaceutical and Clinical Variations Practical advice on the preparation and submission of Variation applications... Learn about: Pharmaceutical Management, Intellectual Property, 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...