Management Forum courses

...Directives and Guidelines Discover where you can find Information on Regulatory Affairs, Approvals, Withdrawals etc Assess the Impact of the EU Clinical... 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: Medical training, Medical Devices, Pharmaceutical manufacturing...

...and performance of a device is pivotal to CE marking a medical device. The collection of post market data is a key aspect of continued safety and performance... Learn about: Medical training, Quality Training...

...Software specification, risk management, architectures, usability and resulting design documentation will be discussed. In addition, practical tips... Learn about: Risk Management, Usability training, Software specification...

...and managers Heads of departments Managers who have received little of no formal leadership training Anyone who wants to develop leadership skills to achieve... Learn about: Medical Devices, Skills and Training, Team Leader...

...Finance Finance Training Administration Management... Learn about: Pharmaceutical Marketing, Life Science, Regulatory Compliance...

...in both the American and European regions. Gain a comprehensive understanding of the processes for the EU and USA, including: EU and US regulatory frameworks... Learn about: EU Regulations, US government, 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: Presentation Skills, Clinical Research, Enhancing Writing Skills...

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

...(both from private practice and industry) In-house Patent and General Counsel Chief Information Officers Chief Technology Officers Business Development... Learn about: European Law, Intellectual Property, US Law...

...This is not just a formal matter, but a substantial issue of first importance. The ‘problem/solution’ approach is not officially part of the EPC... Learn about: Intellectual Property, Life Science, Patent Claims...

...OT329 Solis and ADVAIR DISKUS Asthma UK’s 2016 Annual Report The AOS add-on device as a novel tool to improve powder dispersion Parameters in uencing the... Learn about: Medical Devices, Intellectual Property, Pharmaceutical Marketing...

...for Taking a Medical Device to the Market Place Learn what Regulations Control the Manufacture and Marketing of Devices in the EU Gain an Insight... Learn about: Medical training, Team Training, Quality 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: US Regulations, Medical training, Medical Devices...

...Purpose and Function (incorporating the new EU Signal Analysis Requirements) Developing Company Core System Information CIOMS III Safety Reporting in Licensing... 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, Pharmaceutical Research...

...and current ‘hot topics’. It will also benefit those in departments working closely with the pharmacovigilance department, such as regulatory... Learn about: Medical training, Medical Devices, Legal expertise...

...strategy A practical approach Company and Product Registration Regulations and guidelines New products and line extensions Labelling requirements Registration... Learn about: Medical Science, French Speaking, Pharmaceutical Regulations...

...departments of the pharmaceutical industry, and all those involved in regulatory strategy for submissions to European markets. COURSE OVERVIEW Review of the Variations Regulations... Learn about: Medical Devices, Medical training, Intellectual Property...

...reviewing and/or managing SOPs Ideal as an introduction to preparing, reviewing and implementing SOPs and may also be helpful to those wanting to ensure... Learn about: Confidence Training, Life Science...