Pharma Courses

...European drug master files (EDMF/ASMF) Pharmaceutical development for abridged products Dr Anmar Marouf 12.45 Discussion 13.00 Lunch 14.00 Case Studies... Learn about: Life Science, Pharmaceutical Marketing, Quality Training...

...Overview Combination product Regulation and CTD dossier requirments EU and US (A comparative review) Lecture 2(90 Mins): Clarifying the regulatory requirements... Learn about: FDA perspective, Health Care Provider, Safety Management...

...In order to improve IP performance and to convince management of IP investments, understanding IP key metrics and measuring IP key perfomance indications (KPIs)... Learn about: Sales Training, Sales Techniques, Pharmacy Assistant...

...The program of study leading to the doctoral degree is organized to attain the following objectives: • To enable students to engage in advanced study and... Learn about: Full Time, Information Systems management, Manager Merchandising...

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

...In order to improve IP performance and to convince management of IP investments, understanding IP key metrics and measuring IP key perfomance indications (KPIs)... Learn about: Pharmaceutical Marketing, Sales Training, Sales Techniques...

...all those involved in the Medical Device Industry in the following departments; Manufacturing, Research and Development, Registration, Product Safety... Learn about: Medical training, Medical Devices, Marketing Tools...

...will give an introduction of the EC system for Variations with practical advice on the preparation and submission of Variation applications using the various European procedures... Learn about: Medical Devices, Legal expertise, Intellectual Property...

...with FDA is recommended Be aware of “hot topics” and areas of change This seminar is intended for regulatory, technical, clinical and quality professionals... Learn about: Medical training, US Regulations, Medical Devices...

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

...and administrative personnel. This programme will give you an invaluable overview of the Pharmaceutical industry, from discovery of the molecule through development to marketing... Learn about: Life Science, Drug Development, Pharmaceutical Marketing...

...Practices and in your Current Projects Understand How to Blend Together Both the Technical Aspects of Project Management and the Essential Interpersonal... Learn about: Pharmaceutical Research, IT Project Management, Project Management...

...Process Development Engineers, Scientists, Pharmacists Technology Scale Up and Transfer Managers Validation and Qualification Managers Validation and Qualification... Learn about: Pharmaceutical Marketing, Pharmaceutical Research, Risk Assessment...

...This one-day seminar is designed to help you deal with the difficult people in your working life – the people, particularly colleagues, who can be a minor... Learn about: Medical Devices, Pharmaceutical Management, Life Science...

...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: Intellectual Property, Regulatory Compliance, Life Science...

...led by two highly experienced trainers WHO SHOULD ATTEND Trainee patent attorneys – preparing short or long term to qualify Patent attorneys in private... Learn about: Claim Drafting, Intellectual Property, European Law...

...performance of interactive blends for inhalation Challenges of industrialisation of a novel user friendly DPI Case study: comparing usability of two inhalers... Learn about: Pharmaceutical Marketing, Intellectual Property, Medical Devices...

...COURSE OVERVIEW The demarcation between medicinal products and devices is becoming evermore important. In addition, with the convergence of emerging novel... Learn about: Training planning, Drug Discovery, Legal expertise...

...Clinical trial agreements are one of the most important agreements in the pharma industry as no research can start without the right agreement in place between sponsor and host organisation. They provide a contract which manages the relationship and responsibilities of both parties, and provide... Learn about: Negotiation Skills, Clinical Trial, Legal expertise...

...associates •Junior clinical research associates Course Overview This seminar provides an essential overview of medical device clinical evaluations... Learn about: Adverse Event Reporting, Regulatory Compliance, Medical Devices...