Health and Medicine

The event will bring together internationally recognised biorepositories, scientific pioneers from pharmaceutical companies, and academics to strengthen current knowledge in biosample management and their research applications. Further, the event will dive into application of novel technologies and security software associated to the protection of data. The conference will aim to broaden the understanding of the ethical and regulatory frameworks, as well as defining the impact that the General Data Protection Regulation (GDPR) will have in 2018. The conference also aims at defining some amongst the most successful applications of biosamples in the market. Speakers are the result of a careful…

The use of biophysical methods has become pervasive in the drug discovery process, allowing not only to identify low-affinity hits at the screening stage but also to obtain detailed information on target / ligand interactions at more advanced stages (see the review Renaud et al. 2016 Nat. Rev. Drug Discov. 15: 679-698). This is perfectly illustrated by the success of FBDD (fragment-based drug design), where the progress of biophysical techniques in terms of sensitivity, speed, and automation has been instrumental (see the review Erlanson et al. 2016 Nat. Rev. Drug Discov. 15: 605-619). Indeed FBDD is now widely adopted in…

Conference dates: June 13 – 14th, 2018 Venue: Rio de Janeiro,Brazil This 2 day event features key decision-makers and industry experts from both Pharma & MedTech sectors (in focused streams) to bring attendees an insight-filled event. With plenty of networking opportunities to meet with the LATAM region’s payers & HTAs and experts from industry, this meeting will allow attendees to ensure their market access strategy is optimized for their specific product type. 3 Events in one: 1. Latin American Payer & HTA Forum 2. Pharmaceutical Market Access in Latin America 3. Medical Device Market Access in Latin America

Although an old process, pharmaceutical freeze drying is ever evolving with new trends and approaches being used for pharmaceutical formulation. In it's 6th year, the conference will cover the most recent advances in Freeze drying technology and discuss the latest ideas in the industry. It is the perfect platform to strengthen knowledge in key principles such as PAT and QbD, whilst staying at the forefront of technological breakthroughs to adapt to growing manufacturing demands. Gathering a room of Senior Scientists and Heads of Pharmaceutical Engineering, the 6th annual show provides an ideal forum to discuss the latest advancements in pharmaceutical…

The AI Innovations for Life Science and Health Care Summit taking place June 13–14, in Philadelphia, is the industry only three-track event for those in industry, healthcare, and academia to come together and discuss the practical applications of AI-based, and Blockchain-based technologies and on their daily operations. This event will feature 35+ speakers from across the biomedical landscape and attract leading experts, forward-thinking visionaries, and senior-level executives in life science, healthcare, and technology to uncover the opportunities for AI implementation and the best practices in integrating platforms to achieve desired outcomes. Attendees will walk away with a greater understanding of…

Course "HIPAA Compliance 2018" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: This two day seminar takes the participants through HIPAA compliance from start to compliance. The first presentation explains the history of HIPAA, why it came to being and its evolution. This covers what HIPAA is, what steps have to be performed to be HIPAA compliant and what HIPAA compliance is. It also provides definitions to key HIPAA terms, how to define a Business Associate and how to contract with Business Associates. The second part of…

Risk Elimination. Risk Management. Risk Mitigation. This is the language of upper management, that we as auditors from any industry must learn, if we truly want to effect positive change throughout our environment. During this presentation, the various phases of the audit process will be viewed through the lens of ISO 31000 and ISO 14971. Attendees will learn how to define, recognize, and manage risk through their audit program. Case studies will be reviewed, as we discuss how to incorporate risk management thought, language and techniques into our internal audit process. Areas Covered in the Session : >. Auditing fundamentals…

Product Format: Live Webinar Presenter(s): Stephanie Thomas Conference Date: Wednesday, June 13, 2018 Aired Time: 1:00 pm ET | 12:00 pm CT | 11:00 am MT | 10:00 am PT Length: 60 minutes Price: $227.00 It is important for physician practices to stay current with the latest healthcare revenue collection trends to improve their medical billing services. Join this session, where industry veteran Stephanie Thomas will discuss what it means for your practice to be out of network, and the pros and cons of in-network billing. Thomas will offer tips and tricks on how to get patients to pay their…

Co-located with Next Generation Protein Therapeutics, Cell Line Development And Engineering, June 12-14, 2018 in San Francisco, CA is the event trusted by industry and academic alike. You will hear how peers are overcoming common challenges, implementing new technologies and realizing efficiency gains while working with establishing and developing cell lines. Special All Access Pass allows you entry to both events. Prices: Industry - All Access Pass: USD 2499 Industry - Cell Line Development Only: USD 2099 Academic - All Access Pass: USD 1099 Academic - Cell Line Development Only: USD 699 Speakers: Martina Baumann, Mara Pavel-Dinu, Elizabeth H. Scheideman,…

The 13th Annual Next Generation Protein Therapeutics and Bioconjugates Summit delivers the very latest results from an ever-expanding number of multifunctional molecules in development and offers you the best opportunity to learn from world-renowned academics and industry visionaries who are expanding the frontiers of biologic drugs. Hear from the best and the brightest speakers spanning across industry and academia: FDA Feedback: Regulatory Guidance and Expectations for Next Generation Protein Therapeutics and Bioconjugates Presented by: Christopher Sheth, Supervisory Pharmacologist, Division of Hematology Oncology Toxicology, FDA From Antibodies to Synthetic Proteins Presented by: Sachdev Sidhu, Professor, Donnelly Centre, University of Toronto Lessons…

The Bay Area Pharma Market Research Conference is your exclusive entry into the world of pharmaceutical market research with a focus on the West Coast, yet also considering the global context of the pharma industry. It is the PREMIER event where all the industry's experts network and share knowledge all under one roof. This unique opportunity only happens once a year! Industry insiders say the Bay Area marketplace needs a fresh forum with strong industry representation where senior-level biopharma executives can gather in a comfortable environment, gain insight from premier thought leaders, explore the most critical issues, discuss best practices…

Overview: This includes development of a company philosophy and approach, and incorporating it into the overall computer system validation program and plans for individual systems that have this capability. Why should you Attend: This webinar will help you understand in detail the application of FDA's 21 CFR Part 11 guidance on electronic records/electronic signatures (ER/ES) for computer systems subject to FDA regulations. This is critical in order to develop the appropriate validation strategy and achieve the thoroughness required to prove that a system does what it purports to do. Areas Covered in the Session: System Risk Assessment GAMP 5 "V"Model…

Following the success of the CRISPR Congress in Boston and the launch of CRISPR Congress in Berlin, we are now building a CRISPR community on the West Coast for the genetic/gene editing research community in addition to getting into the burgeoning stem cell market The inaugural Precision CRISPR Stem Cell Congress Seattle 12-14 June 2018, founded in partnership with the Allen Institute, will help the large pharma, biotech and academic community overcome efficiency, specificity and delivery challenges to optimise the application of CRISPR gene editing of stem cells. Showcasing cutting edge data from key opinion leaders who are pushing the…

Course "Applied Statistics, with Emphasis on Verification, Validation, Sample Size, and Risk Management, in R&D, Manufacturing, and QA/QC" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: The 2-day seminar explains how to apply statistics to manage risks and verify/validate processes in R&D, QA/QC, and Manufacturing, with examples derived mainly from the medical device design/manufacturing industry. The flow of topics over the 2 days is as follows: • ISO standards and FDA/MDD regulations regarding the use of statistics. • Basic vocabulary and concepts, including distributions such as binomial,…

ESS 2018 is committed to excellence as the conference gives everyone working in the area the opportunity to come together to share information and network with colleagues. The programme has been designed as a training platform for Therapists, Nurses, Therapy Assistants, Clinical Engineers, Clinical Technicians, Suppliers, Managers, Healthcare Professionals and Students to participate in the Seating and Assistive technology assessment and provision process. The conference is suitable for foundation, intermediate and advanced levels of knowledge. The acclaimed speakers will travel from around the world, and are leading professionals in the areas of Specialised Seating and Assistive Technology, Occupational Therapy, Physiotherapy…

Product Format: Live Webinar Presenter: Dorothy D. Steed, CCS, CDIP, COC, CPCO, CPUM, CPUR, CPHM, CPMA, ACS-OP, CCS-P, RCC, RMC, CEMC, CPC-I, CFPC, PCS, FCS Conference Date: Tuesday, June 12, 2018 Aired Time: 1:00 pm ET | 12:00 pm CT | 11:00 am MT | 10:00 am PT Length: 60 minutes Price: $197.00 Behavioral health challenges are frequently identified in primary care or emergency center encounters. How does the behavior affect management of medical problems? Join this session, where auditing and training expert Dorothy D. Steed will review multiple types of behavioral health encounters and documentation elements that payers seek…

Changes in the FDA’s regulation of software makes life a lot easier for medical device manufacturers. FDA faced an overwhelming challenge when it started to develop a regulatory program beyond the basic Quality System regulation and the Software Guidance issued in 2002. Congress and FDA have made huge changes in FDA’s legal jurisdiction, and FDA has made dramatic revision of its regulatory program. FDA no longer regulates low risk software, premarket guidance documents must be revised or withdrawn, firms can give themselves 510(k) market clearance rather than FDA, firms can substitute requirement of Reports of Corrections and Removals by participating…

Operating a commercially viable chemical process requires a good chemical synthesis to start with, but is also subject to the interplay of a myriad of important physical phenomena - heat transfer, mass transfer, fluid flow, etc. which are traditionally the realm of the chemical engineer. An understanding of these scale-up phenomena is crucial for the laboratory development of processes that will scale successfully. This course presents an overview of these issues and examines their impact on process operation in the pilot plant and beyond, including scale-up considerations for route selection, raw material charging, reaction steps, workup, crystallization, product isolation, drying,…

Developing safe processes is of paramount importance to any chemical company. Exothermic chemical reactions in batch and semi- batch processes can result in serious injury to people and plant if they get out of control. Results of thermal runaways include violent loss of containment, possibly explosion and the release of flammable or toxic materials to the environment. Employers are bound by Health and Safety legislation to ensure the safety of their employees and those outside their employment who might be affected by their activities. Chemical manufacturers must therefore be aware of all potential dangers in their processes and take steps…

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