Management Forum courses

...An Overview of Pharmaceutical Regulatory Affairs for Support Staff. Key Topics to be be covered:- Understand the Background of EU Law – Regulations... Learn about: Directives etc, EU Law, IT Law...

...Past delegates include personnel from the following departments:- Regulatory Affairs Pharmacovigilance Quality Assurance Technical Support This seminar... Learn about: Medical training, Pharmaceutical manufacturing, Medical Devices...

...compliance This course has been designed specifically for those who are involved in gathering clinical evidence required for medical devices and in-vitro diagnostic products... Learn about: Quality Training, Medical training...

...practical tips on how to streamline the development process, understand the regulatory requirements and how Notified Bodies review Technical Files will be covered... Learn about: Medical training, Risk Management, 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: 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, Life Science, Regulatory Compliance...

...This course provides a comprehensive understanding of how to develop a veterinary medicine in the EU and USA. Different approaches taken by the regulatory... Learn about: Animal Nutrition, Drug Development, EU Regulations...

...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: Enhancing Writing Skills, Presentation Skills, Clinical Research...

...COURSE OVERVIEW This seminar combines one day of claim drafting fundamentals with a further day of focused workshops. Attendees have the choice of either... Learn about: European Law, Intellectual Property Law, Intellectual Property...

...public debate about whether patent protection should be available for software-related and business-related inventions WHO SHOULD ATTEND Patent attorneys... Learn about: US Law, Life Science, European Law...

...Clarity is required to distinguish the subject matter of a claim from prior art, and an unclear claim can be interpreted to the disadvantage of the applicant or proprietor... Learn about: Patent Claims, IT Law, Life Science...

...development and associated studies. This conference aims to: address many of the issues around generic inhalers, provide case studies of bioequivalence testing... 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: Team Training, Medical training, Quality Training...

...Upon completion of this seminar, participants will: Understand the overall FDA medical device regulatory process Know what is required for 510(k)... Learn about: Medical Devices, Pharmaceutical Regulations, US Regulations...

...ATTEND Expand your global safety knowledge Enhance your team’s capabilities and compliance in both the regulations and your company’s expectations Help... Learn about: Risk Management, IT risk...

...The Pharma 3 day Mini MBA accelerated management programme is a distillation of the most valuable parts of an MBA, as applied to the Bio/Pharmaceutical industry... Learn about: Veterinary science, Pharmaceutical Research, Intellectual Property...

...WHO SHOULD ATTEND This interactive course will benefit you if you are involved in the daily practice of pharmacovigilance and are looking for an update... Learn about: Medical training, Intellectual Property, Life Science...

...samples and certification/legalisation Compilation of the Dossiers* Contents and formats Hints on success/failure Specific country requirements Regulatory... Learn about: Medical training, Medical Science, Pharmaceutical Regulations...

...guidance on how they are being implemented. The meeting is addressed to clinical and pharmaceutical personnel in the registration and regulatory affairs... Learn about: Pharmaceutical Management, Intellectual Property, Medical Devices...

...An Essential course for ensuring compliance with regulatory requirements SOPs play a crucial role in helping with organisational operational efficiency... Learn about: Confidence Training, Life Science...