Your step-by-step guide to interpreting the impact of CFPP0106 on your endoscopy services Arm yourself with the necessary skills and procedural practices to meet standards head-on. This interactive masterclass is your opportunity to clarify what you can and should be doing to ensure safe and effective decontamination processes for your flexible endoscopy services. CFPP0106 needs to be understood and translated for every endoscopy department up and down the country. Only at this event will you hear: Clarification of the impact CFPP0106 on your trust services Practical advice on how to overcome common hurdles and trip points Where there is room…

Attend this NHS Cancer Conference, designed to enable you to manage demand, meet national cancer standards and drive forward your service. A unique event focused on NHS cancer service delivery, this one day event will offer unrivalled insight into the innovative strategies trusts around the country are successfully incorporating to meet national standards and deliver better care. Modernise your service to deliver enhanced patient outcomes: Drive forward change: achieve both long term and short term national cancer goals Employ enhanced recovery: how to reduce length of stay and improve patient outcomes Identify the practicalities of offering day surgery: overcome safety…

This 90 minute live, interactive webinar will review the dietary supplement regulations and discuss how to verify that your products are compliant, while citing differences with food and drug regulations. We will also cover what qualifies a material as a dietary ingredient, considerations for manufacturers and distributors, requirements for compliant labeling and acceptable marketing claims. An update on FDA’s draft guidance for New Dietary Ingredients and an overview of the Dietary Supplement Labeling Act (both introduced in 2011) will also be discussed. At the conclusion of this 75 minute presentation, there will be a 15 minute Q&A session with the…

Expectations for meaningful hazard analysis, hazardous conditions, and documentation have always existed by regulatory agencies. There is an increased awareness of the importance of design activities to support the production of safe and effective product. Product risk management is a required tool to drive and direct resource constrained product design, manufacture and validation activities in the company. High-profile field problems indicate that such activities are not yet adequately planned executed, and visibility maintained. There is a failure to fully utilize the power of current risk management tools. Effective use of such risk management tools can help address the growing push…

Your unique Acute Oncology development event: progress your understanding of the key requirements Following on from the success of our interactive masterclass ‘How to Plan and Implement your Acute Oncology Service’ this seminar has been designed to take the theory one step further. Join us now as we take a deeper, more progressive look at Acute Oncology and how to sustain a workable service whilst consistently delivering excellent outcomes. Do you have a model in place for your acute oncology service? Are you fine tuning or continuing to develop your plan? Are you beginning to think about sustaining and auditing…

This focused day has been specifically designed for Breast Cancer Care professionals who are responsible for reducing the breast cancer pathway. If this is you, then don’t miss out on an unique opportunity to identify the realities of reducing your average length of stay with this practical ‘how to’ insight into delivering a 23 hour patient pathway. Set the foundations for improved outcomes by learning how to: • Establish a successful 23 hour patient pathway: identify the logistical process for set up • Refine your procedures from admission to discharge: focus on pre-op for successful post-op • Manage the whole…

There is a pervasive public perception that the FDA has been ineffective in protecting the public. Recent news events seem to support this perception. The FDA is working hard to change that perception. Industry must be prepared to adapt, and recognize that such adaptation will actually work to their long-term benefit. This webinar will discuss and evaluate the effects that this call for change has on a company and its selection, audit, use and on-going relations with its suppliers of services and products / components. What are the "new" expectations for the COA and COC? How can companies address the…

Now, in its 5th year the Pharma Resource Planning and Portfolio Management event will build upon our previous years by continuing the focus on overarching portfolio management instead of individual project management, but will look more in-depth at resource building to keep operations in-house, strategies for a more productive portfolio review process and more consideration of the market conditions looking ahead using forecasting techniques. Delegates will also hear from a wide variety of relevant perspectives beyond branded pharma including med device, biotech, generics and consumer healthcare experts. Delegates will leave the conference with strategies to improve their resource allocation programs…

"Grief and Loss in Addiction and Recovery" will be presented on Tuesday February 28, 2012, from 7:30 pm to 9:00 pm; by Janice Firn, LMSW, Clinical Social Worker, University of Michigan Hospital; and Matthew Statman, LLMSW, CADC, Dawn Farm therapist and Education Series Coordinator . This program will describe Worden's and Kubler-Ross' theories of grief and grief recovery, losses that the chemically dependent individual and his/her family experience throughout the addiction and recovery processes, and how recovery program tools can help individuals cope with grief and loss. This program is part of the FREE, annual Dawn Farm Education Series. Our…

Expert neurologists and cardiologists from around the world will convene in the heart of Paris for the inaugural International Conference on Heart & Brain.

N&G 2012 will enable the exchange of ideas and knowledge between the different disciplines for facilitating research and clinical interdisciplinary collaborations focusing on nutrition and growth.

Overview: Attend this webinar to understand the differences and benefits of verification and validation. Learn about the risks and complications involved with the application of sound verification and validation principles. Why Should You Attend: The meanings and regulatory requirements of the terms "verification" and "validation" are often confusing to engineers and even some regulatory professionals. FDA regulations as well as European standards such as ISO 13485:2003 require both verification & validation documentation throughout these regulations and standards.The terms apply to design control, process control and others. Verification and validation also appear in the "essential requirements" in MDD 93/42/EEC needed for…

IOMC 2012 is the 5th International Online Medical Conference that will take place on March 3, 4, 10 & 11, 2012. IOMC is one of the most innovative conferences which has been increasingly welcomed by medical & healthcare experts, researchers, professionals, students, and professors from around the world. Building upon the success of previous IOMC conferences since 2007, IOMC 2012 aims to foster the discussion among medical, nursing and healthcare researchers and provide them with the opportunity to discuss and present their research findings, studies, and experiences at a professional level and share their research works with the world. Authors…

Excellent opportunity to explore the most imoprtant aspects of diagnosis, research and treatments in psychiatry and neuropsychiatry fields today.

XIII Pan American Congress of Neurology

Overview: This training course is designed to give pharmaceutical and biologic companies operating in the U.S. and EU an understanding of product safety and regulatory compliance. The course will include case studies of adverse events to illustrate the decision-making process and reasoning needed behind when and how to properly report incidents to regulatory authorities. Product safety makes headlines every day - and the impact on a company’s image, consumer confidence, and Wall Street’s opinion is profound. While good safety data has historically been a prerequisite for product approval, recent media attention has intensified public and Congressional scrutiny and resulted in…

"Teens Using Drugs: What To Know and What To Do" is a free, ongoing, two-part series designed to help participants learn to understand, identify and address adolescent alcohol/other drug problems. Part 1 provides information on how to understand and recognize the signs of a teen substance abuse problem and includes a short video. Part 2 provides information on what should and should not be done when a teen substance abuse problem is recognized, and concludes with a short open talk by a young person in recovery. The series is presented on the first (part 1) and second (part 2) Tuesday…

Traumatic Brain Injury (TBI) is a major cause of death and disability globally and is considered a serious public health problem. In the US, an estimated 1.7 million people sustain a TBI every year, and over 30 percent of all reported injury-related deaths list TBI as a contributing factor. Moreover, mild traumatic brain injury is the most common combat-related injury and along with spinal cord injury, TBI accounts for nearly 25 percent of combat casualties. Treatment of TBI and especially acute TBI is still a major unmet medical need. Therapies that prove an ability to limit the damage done to…

NHS clinical research contracts Delivering you practical insight and key legal advice on how to ensure watertight robust agreements Are you responsible for managing clinical research contracts for your site? Do you want: more guidance on how to craft strong agreements? understanding of the range of clinical studies and their different contracting needs? to develop organisational level agreements with strategic partners? practical insight and expert advice on common legal hurdles and trip points? Yes! Then this interactive seminar has been designed for you. This day will ensure that you fully understand the practical realities of clinical research contracts. Develop your…

Overview: This webinar details both regulations and provides details for implementing computerized systems. Learn exactly what is needed to be compliant for all three primary compliance areas: SOPs for the IT infrastructure, industry standards for software product features, and the 10-step risk-based validation approach. This webinar demystifies Part 11 and the new European equivalent Annex 11. It gets you on the right track for using electronic records and signatures to greatly increase productivity. Areas Covered in the Session: Which data and systems are subject to the regulations? What the regulations mean, not just what they say. Avoid 483 and Warning…