Health and Medicine

Training Options Duration: 3 Hours Wednesday, September 26, 2018 | 09:00 AM PDT | 12:00 PM EDT Overview: We will review each of the elements of the physician employment agreement in depth, focusing on the pitfalls and the problems that can develop when the agreement does not clearly define the relationship, and/or when the parties do not fully understand what is being agreed to. Such items as term and termination, termination for cause, duties of the physician, call, non-compete, and compensation are all items that should be clearly set out in the agreement and fully understood by the parties. Why…

Description: Senior management takes responsibility for Quality and GXP compliance. It is not something delegated to the Quality unit or to the Regulatory Affairs group. Developing and implementing an effective Inspection readiness plan will help ensure better results, as well as a less stressful inspection. Planning strategically ahead will reduce document turn-around time, improve presentation skills from SMEs, and increase inspector confidence in the Quality System. Successfully completing an FDA inspection is critical to cGMP operations and commercial success. Implementing and maintaining robust quality systems is one element to accomplishing this goal. However, it is not the only element. Inspection…

Join Us for dinner and this very important program we are bringing to Winter Park, Florida! This CME/CE/CPE-certified program is intended for physicians, nurse practitioners, physician assistants, registered nurses, pharmacists, and other healthcare providers who care for patients with multidrug-resistant Gram-negative infections. The goal of this activity is to improve participants' knowledge and competence in applying current and emerging antibacterials in the management of patients with resistant Gram-negative infections. Speakers: Lilian Abbo, MD, Debra Goff, PharmD, FCCP Time: 6:30 pm - 8:00 pm

Themenschwerpunke: Pneumologie / Allergologie, Hamatologie / Onkologie, Diabetologie, Endokrinologie, Geriatrie / Palliativmedizin, Infektiologie / Immunologie, Notfallmedizin / Intensivmedizin, Gastroenterologie / Hepatologie, Nephrologie / Rheumatologie, Kardiologie / Angiologie In 3 Tagen UP-TO-DATE in der kompletten Inneren Medizin - geeignet fur Kliniker ALLER Fachrichtungen mit Interesse an Innerer Medizin - komprimiertes 3-Tage-Curriculum - auch Einzeltage buchbar (nicht besuchte Fortbildungsmodule on demand erhaltlich) - samtliche Schwerpunkte der Inneren Medizin - konzentrierte Vermittlung durch ausgewiesene Experten - unabhangiges wissenschaftliches Programm - unmittelbare Einsetzbarkeit im klinischen Alltag - 24 CME-Punkte erwartet URL: Tickets: https://go.evvnt.com/171731-1?pid=154 Time: 8:30 am to 6:00 pm Prices: 1-Tages-Ticket Assistenzarzt: EUR 195.0,…

New or existing modified drug Stability Testing Program's regulations/requirements stipulated by the FDA, 21 CFR or other regulations may sometimes creating an overwhelming situation based on the type of product that is being manufactured. Hence, some manufacturers of new drug products have made inadvertent mistakes in the design of their new drug stability testing program. Such mistakes may ultimately delay the new, existing or modified product IND or NDA application process due to the data that was presented to the FDA (i.e. Relevant aspects of the stability testing program requirement may have been omitted by the drug manufacturers). It is…

Join Oxford Global for the 16th Annual Pharmaceutical IT Congress, 25-26 September 2018, London where over 250 attendees will be representing global pharmaceutical organisations, leading biotech companies and internationally renowned academic institutions. Across two days, we will bring together 27 presentations and case studies focusing on the key development in Big Data, R&D informatics, translation informatics, NGS informatics and bioinformatics, and real-world evidence and real-world data. Including 3 interactive streams: • Big Data Led Strategies & Innovation • R&D Informatics, Translational Informatics, NGS Informatics and Bioinformatics • Management of Real-World Evidence and Real-World Data View Agenda: http://bit.ly/2nLs4cc For further information…

Join Oxford Global for the 2nd Annual Artificial Intelligence in Drug Development Congress, 25-26 September 2018, London where over 250 artificial intelligence and pharmaceutical IT attendees with represent leading biotech companies, global pharmaceutical organisations and internationally renowned academic institutions. Across two days, we will bring together 30 presentations and case studies focussed on the innovatice application of artificial intelligence in drug discovery and discovery chemistry, alongside machine learning in clinical trials and cloud computing. Including 3 interactive streams: • AI in Drug Discovery and Discovery Chemistry • Machine Learning and Personalising Patient Treatments • AI in Big Data and Clinical…

The European Society for Vascular Surgery (ESVS) is a non-profit organization which strives to relieve sickness and to preserve and protect health by advancing, for the public bene
t, the science art and research into vascular disease, including vascular surgery. The Society's 32nd Annual Meeting will take place on 25-28 September 2018 in Valencia, Spain. The rich scientific programme of the Meeting will include state of the art lectures, interactive symposia led by renowned international experts, 160 rapid-fire presentations and more than 100 poster presentations selected from abstract submissions, scientific sessions gathering the very best of recent research and innovative science…

Participants will review case histories, examine images by virtual microscopy, and formulate diagnoses. The unique subtleties and differentiating characteristics of each diagnosis will be highlighted. Participants will also discuss the patient management strategy used in each case. During the four-day conference, 37 cases will be presented and discussed. Three to four specialty areas will be featured each day to include: Head and Neck Pathology Bone and Soft Tissue Pathology Breast Pathology Cytopathology Dermatopathology Endocrine Pathology Gastrointestinal Pathology Gynecologic Pathology Infectious Disease Liver Pathology Prostate Pathology And important surgical pathology practice issues and concerns Prices: Physicians/Scientists: USD 1100.0 Residents/Fellows/Allied Health: USD…

The MENA region has made remarkable progress in its healthcare landscape over the past years. With the insurance industry witnessing evolution, countries in the MENA region are now at different stages of rollout and adopting different models of mandatory health insurance. Strategic reforms and initiatives to provide affordable access to healthcare services and a commitment to improve the population’s health has made the health insurance an important segment in the region’s economy. The MENA Health Insurance Congress is a strategic platform to meet and hear from top notch leaders, policy and decision makers from all over the region who will…

As we see more and more oncology products failing in the clinic there needs to be a revolution in the way we conduct our preclinical and translational research. Tumor Models Shanghai is the platform that will bring together experts from Pharma and Biotech from across Asia to discuss the vital challenges currently facing industry. By joining us you will get access to insight into the in vivo models that are driving research forward. Including, information on the newest in vivo models, deep dives into the prediction and overcoming of resistance mechanisms, the optimisation of model and target selection rationale; and…

If you're actively invested in leveraging evidence to support drug development and commercialization, join the 6th annual IMPACCT:RWE 2018 meeting, where you will have an opportunity to explore how RWE is currently applied across the drug development continuum to support decision-making in clinical development, drug marketing and commercialization. Today more than ever, we live in a world of mobile, digital and electronic generated data. In healthcare, real-world data provide great potential for better design and conduct of clinical trials and generate more value-based outcomes in drug development. To gain competitive advantage and achieve better outcomes, pharma and biotech organizations seek…

DPharm is where the clinical trials industry gathers to report on the latest disruptive and innovative projects to advance clinical trials. DPharm 2018 is the year of patient data ownership, all things digital, and new approaches to optimize clinical systems. Co-chairs Dr Sylke Poehling, SVP and Global Head, Strategy, Portfolio and Clinical Operations, Roche, Dr Andreas Koester, VP and Global Head, Janssen Clinical Innovation, Janssen, and Craig Lipset, Head of Clinical Innovation, RandD, Pfizer, Inc, host 70+ speakers, who are challenging conventional thinking and inspiring new ideas to reduce the burden on patients, investigators and sites. DPharm is divided into…

Overview: This course offers practical approaches and models to address human performance issues in GMP related environments by using a specific methodology to correct, prevent and avoid re-occurrence of these issues. Why should you Attend: This training would provide tools that can be implemented and used after this event. This includes practical tools. We will discuss human error categories, near root causes and root causes for these events. We will discuss latest trends in human error issues in the industry. Areas Covered in the Session: Background on Human Error Phenomena Importance of Human Error Prevention/reduction Training and human error Facts…

Overview: Project risk is greater the longer your project lasts, the longer the time between preparing your project plan and starting the work, the less experience you, your team members, or your organization may have with similar projects, and the newer your project's technology. Why should you Attend: This webinar is the fifth in a series of webinars that detail all of the critical aspects of project management. The contents of each webinar in this series are designed to mirror the key sections of the PMP exam. The subject of this webinar is assessing and planning for risk. This webinar…

“Advances in collaborative research for public health, medical and medicine sciences for better healthcare services to society” The conference will cover vital issues in medical, medicine and health sciences under multiple sub-themes. The aim of our conference is to support, encourage and provide a platform for networking, sharing, publishing and nurturing the potential growth of individual scholars across the globe.

“Addiction and Families” will be presented on Tuesday September 25, 2018; from 7:30 pm to 9:00 pm; by Lynn Kleiman Malinoff, Ed.D. Alcohol/other drug addiction is often described as a “family condition.” Each member of the family unit is affected by addiction within the family and often family members have challenges in supporting each other and taking care of their own health and well-being. To survive within a framework of chaos, family members often develop roles and defense mechanisms that help them to cope. Family involvement is an important element of the recovery process for people with addiction, and family…

The leading U.S. event devoted to building the skills, speed and teamwork of your promotional review committee members will take place September 24–26, 2018 in Morristown, NJ. This year's three-day event, for the first time, will offer an in-depth, interactive workshop featuring insights from an OPDP reviewer. By learning from their thought processes, you can better understand how OPDP takes claims apart and how regulatory analysis may come down against you if you don’t have the right evidence. The 6th Promotional Review Committee Compliance and Best Practices conference is set to bring together more than 100 professionals to ensure your…

Top Five Reasons to Attend: - Understand FDA updates on the implementation of generic drug labeling requirements - Discuss annual reviews of CCDS; self-audit of labeling vs. CCDS - Share best practices on how to manage the end-to-end process of labeling and packaging products - Review the product labeling processes and procedures used to establish effective label design - Explore challenges in CDS, carton and container labeling development Who Should Attend: This conference is of interest to professionals from pharmaceutical, biotechnology and medical device companies with responsibilities in the following functions: - Labeling - Drug Safety - Regulatory Affairs -…

The 5th annual Mobile in Clinical Trials is full-day conference preceding DPharm: Disruptive Innovations to Advance Clinical Trials and goes into detail on: - Real-time implementation of mobile solutions trials driving efficiency - How to scale up - Perceived barriers and how to overcome them - Moving past the hype of mhealth and producing evidence - Optimizing the true value of mobile data - Mobile 2.0, wearable, sensors, apps and mobile devices Morning Sessions Program chair Dr Dan Karlin, Pfizer, presents the opening remarks for the event. The morning includes industry sessions on: Bayer's perspective on the good the bad…