Health and Medicine

HR audits are designed to help your organization focus its attention on its human resource management practices, policies, procedures, processes, and outcomes by providing you with a structured and systematic series of questions about key compliance, risk management, internal auditing, and human resource management issues. As a process, HR audits are designed to help your organization identify potential and actual problem areas, help assess the effectiveness of current HR management activities, help assess weaknesses in HR internal control processes, and help assess human capital strategic and compliance related risks. HR audits should additionally provide suggestions for corrective action. Importantly, HR…

This lesson will be addressing how practice/business managers (or compliance officers) need to get their HIPAA house in order as HIPAA is now fully enforced and the government is not using kid gloves any more. It will also address major changes under the Omnibus Rule and any other applicable updates for 2018 and beyond. There are an enormous amount of issues and risks for covered entities and business associates these days. I will speak on specific experiences from over 17 years of experience in working as an outsourced compliance auditor, expert witness on multiple HIPAA cases, and thoroughly explain how…

Drug dissolution testing is an essential and critical step for appropriate and efficient product development such as tablet and capsule. A number of approaches are used to conduct dissolution testing using different apparatuses and methods. Making a choice for an appropriate apparatus and method has always been confusing and challenging. This seminar will provide relevant pharmacokinetics and physiological background so that making this choice becomes easier and instinctive. No prior knowledge of pharmacokinetic and/or physiology is required; however, these will be explained in very simple terms to help attendees in selecting or developing a dissolution method. This seminar will describe…

Global Medical Device Regulations continue to evolve, as devices become more diverse and sophisticated. Understanding the regulations and requirements in your targeted markets will expedite speed-to-market of innovative products and assist patients needing access to life-saving products and technologies. Government Regulatory Authorities, needing to become more efficient with their time, are looking for ways to better use their internal resources without compromising safety in products, which become marketable. One such example is the Medical Device Single Audit Program [MDSAP], where Authorized Organizations would be allowed to carry out a single GMP audit on medical device manufacturing facilities and have it…

Classification systems differ from that of the United States or European Union in select countries Medical devices are classified depending on their risk level Medical devices must also comply with additional country standards and these standards define industry-wide safety and performance requirements Regulatory registration process is defined for China, Hong Kong, India, Japan, South Korea, Taiwan, Singapore and Australia The regulatory process from product design to market entry for a new medical device or IVD is oftentimes complicated and unclear. In Asia Pacific, it can become difficult to make a clear distinction between your regulatory strategy and business strategy. And…

This course teaches participants the fundamental concepts and methods needed to establish effective control charts and estimate process capability. In addition to learning traditional control charts (e.g. xbar, r/s), participants will be exposed to other useful charts for handling multiple sources of variation (within/between) and short production runs. Practical aspects of implementing SPC on the shop floor are also discussed. Estimating process capability for both normal and non-normal data is discussed. The meaning and limitations of popular capability are presented in detail. This highly interactive course will allow participants the opportunity to practice applying SPC techniques with various data sets.…

Course "Validation and 21 CFR Part 11 Compliance of Computer Systems" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: Computer Systems Validation (CSV) also known as Software Validation is all-pervasive in the Life Sciences Industry. It is a requirement of all the predicate rules, as well as 21 CFR 11 and Annex 11. However, unless one knows how to implement CSV, it is often very hard to detect the requirement for CSV, and very hard to determine what needs to be done, to meet domestic and /…

About ICPHMS2018 2018 3rd International Conference on Public Health and Medical Sciences (ICPHMS2018) (http://www.icphms.com) is a platform for academic communications between specialists and scholars in the fields of public health and medical sciences. ICPHMS2018 will be held in Hangzhou, China during May 29-31, 2018. Hangzhou is the capital of Zhejiang Province and one of the seven ancient capitals of China. Publication 2018 3rd International Conference on Public Health and Medical Sciences (ICPHMS2018) accepts original and unpublished papers. Both Full paper and Abstract are welcomed. Full papers accepted by the conference will be published online in the following journals of Science…

The pharmaceutical industry has an array of duties of keeping up with technology and research as well as the unbridled counterfeit products that can thwart the efforts. The snide, intended to mimic the genuine products, have in many cases led to lack of effective healing, adverse reactions and now the diminishing confidence in medicines and the general healthcare systems and the providers of the same. With sales ranging from €150 billion to €200 billion which is US$163 billion to $217 billion every year, as indicated by industry estimates, fake pharmaceuticals are the most lucrative segment of the worldwide exchange illicitly…

The 9th World Orphan Drug Congress is Europe's meeting place for the rare disease community. The Conference offers strategic keynote plenaries, themed tracks and dedicated networking sessions, you have the chance to really tailor the event to the needs of your day-to-day role. Exhibitors have a unique opportunity to put their business products and services in front of potential buyers looking to source the latest technologies in the orphan drugs industry. Meet and listen to biotech start-ups and investors in our Pitch & Partner track where the most promising companies showcase their orphan drug technology and pipeline. The Congress was…

The two day workshop is designed to provide an in-depth understanding of the concept of pharmaceutical validations based on the current FDA, EU and ICH guidance documents as well as learnings from the pharmaceutical industry. Special emphasis will be laid on practical approach and simple illustrative examples from the industry for judicious and effective implementation. The participants will be exposed to the latest concepts and thinking of international regulatory agencies on validation of manufacturing process, analytical as well as cleaning methods applicable in API & Oral Solid Dosage forms manufacturing. based on assessed risk. The workshop will also include typical…

Short Description : The two day workshop on GMP for Quality Control Laboratories and FDA Audit Preparation, is designed to provide an in-depth understanding of the regulatory background and guides attendees through all critical areas of GMP compliance. You will gather a thorough awareness of latest trends and updates with respect to USFDA, EU, WHO and PIC/S (Pharmaceutical Inspection Co-operation Scheme) and Indian GLP Schedule L1 compliance and guideline requirements. This course will also provide examples to develop inspection ready documentation. Full description : On completion of this course, the participants shall be well versed with the global Quality control…

The PharmAccess Leaders Forum is Europe’s most respected event for stakeholders involved in achieving patient access for innovative medications. Experience 2 days of networking, partnering and engaging Europe’s top stakeholders to achieve enhanced market access and better demonstrate your product’s value to payers. 3 Events in one: 1. Pharmaceutical Payer & HTA Forum 2. Innovative Pricing and Reimbursement Agreements 3. HEOR Evidence Excellence

Hundreds of thousands of patients receive cardiac rhythm devices each year for brady or tachyarrhythmias and heart failure. In addition, the number of people who may benefit from an implantable cardioverter defibrillator (ICD) and/or cardiac resynchronization device (CRT) has substantially increased in the past decade. Evolving device technology has increased programming complexity, follow-up, and management. Cardiac implantable device management related to electrophysiology remains a major part of daily practice for cardiologists, electrophysiologists, and non-physician caregivers involved in the management of these devices. Presentations will highlight the following: 1. Update on cardiac pacing technology 2. Review information for device management germane…

The NCRI Cancer Conference is the UK’s largest forum showcasing the latest advances in cancer research. The Conference provides a platform for researchers, clinicians, people affected by cancer and industry representatives to come together to discuss, present and showcase high-quality research. Informative and interactive sessions attract over 1,500 delegates each year and create the ideal setting to establish new collaborations with key stakeholders in cancer research. Price: Range from: GBP 150 Booking https://go.evvnt.com/180579-1?pid=154 Speakers: Charles Swanton, Fiona Powrie, KJ Patel, Quynh-Thu Le, Malcolm Dunlop, Richard Gilbertson, Sam Gambhir, Stefano Piccolo Time: on Sunday November 04, 2018 at 9:00 am (ends…

Science Access invites all the participants from all over the world to attend “International Conference on Biotechnology" to be held during June 25-27, 2018 Rome, Italy. The conference covers with the theme: “Novel Trends and Innovations in Biotechnology” Biotechnology Conference 2018 gives an immaculate stage to bring out such quality research works. These gatherings are stretched out by commenting key administrative ranges like Multi-disciplinary biotechnology. Giving a possibility, Science Access biotechnology Conferences have researchers, analysts, substance associations and all agents of pharmaceutical and science organization divisions can exhibit their apt discoveries and in the meantime get presented to a helpful…

Catheter ablation is an important therapy for atrial and ventricular arrhythmias. Catheter ablation is now an established first line therapy for many supraventricular tachycardias and ventricular arrhythmia's in patients with structurally normal hearts. Although the approach to many of these arrhythmias is straight forward, all practitioners encounter challenging cases due to anatomic and pathophysiologic variations. This course will provide comprehensive instruction for diagnosing common and complex cardiac arrhythmias in the electrophysiology laboratory and achieving effective and safe ablation. Case-based illustrative presentations will highlight diagnostic dilemmas and key management strategies. Experts discussing detailed patient cases provide a step-by-step analysis and in-depth…

Science Access invites all the participants from all over the world to attend “International Conference on Pediatrics" to be held during September 10-12, 2018 Amsterdam, Netherlands. The conference covers with the theme: “Exploring the potential outcomes and novel advancement in the field of Pediatrics” Pediatrics is a global platform to discuss and learn about health, Neonatal Intensive Care, Pediatric Immunology, Pediatric Infectious Diseases, Pediatric Oncology, Pediatric Hematology, Pediatric Allergy, Pediatric Pulmonology, Pediatric Cardiology, Pediatric Neurology, Pediatric Endocrinology, Pediatric Gastroenterology, Pediatric Urology, Pediatric Psychology, Pediatric Surgery and Pediatric Emergencies.

This course will be focused on heart failure seen in daily clinical practice. The program will be primarily case based with a few supplemental lectures covering the bread and butter for heart failure, novel therapies, hospital readmission and advanced heart failure. Save the date to spend a 1.5 days with faculty for an update in heart failure management and enjoying the land of 10,000 lakes. Price: Registration Fee: USD 395 Speakers: Brooks S. Edwards M.D., Daniel D. Borgeson M.D. Time: 8:00 am to 12:00 pm

Conference Series invites all the global participants to attend 8th International Conference on Health and Medicine scheduled during October 08-09, 2018 in Osaka, Japan. Health Summit 2018 is a forum that brings together decision-makers, community leaders, innovators, and influencers aims to improve health all over the globe. for more info : https://medicaleducation.healthconferences.org/