Conférences - Système de santé, gestion hospitalière

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1
Managing Your FDA Inspection: Before, During and After
02 avr 2020 - 03 avr 2020 • Chicago, IL, États-Unis
Organisateur:
Complianceonline
Résumé:
The course will cover the factors used by the FDA to schedule inspections. You will learn how to predict what an FDA investigator will do and what they will cover in the inspection. There should be no surprises if you have prepared properly. Firms need to understand the details about inspectional techniques to avoid making new problems for yourself during the inspection. You can save yourself a lot of corporate misery if you know what to do before, during and after an inspection
Contact:
Tél.: [18887172436];     Email.: referral@complianceonline.com
Sujets:
FDA inspection seminar, FDA inspection, FDA 483, FDA warning letter, FDA investigator, FDA law, Regulatory Sanctions used by FDA, Prohibited Acts, Management Responsibility from FDA’s view, FDA Inspection Team, FDA Inspection SOP, FDA Meeting, FDA inspection Scribes, Warning Letter Responses, import alerts, inspection documentation
Identifiant de l'évènement:
1324669
2
Method Development and Validation for Assays Supporting Testing of Biologics
02 avr 2020 - 03 avr 2020 • Orlando, FL, États-Unis
Organisateur:
Complianceonline
Résumé:
Biologics continue to be a steadily growing component of the pharmaceutical industry. The advent of large molecule therapeutics requires a different perspective on the assays needed to support development through preclinical and clinical testing.
Contact:
Tél.: [18887172436];     Email.: referral@complianceonline.com
Sujets:
Attend this biologics seminar to learn essential concepts related to cell-based potency methods, ELISA, immunogenicity methods, analytical CMC methods, cell culture procedures, immunogenicity methods, and biomarker validation
Identifiant de l'évènement:
1329150
3
Supplier and Contract Manufacturer Management
02 avr 2020 - 03 avr 2020 • Orlando, FL, États-Unis
Organisateur:
Complianceonline
Résumé:
Effective management of suppliers and contract manufacturers is an integral component of a quality management system. Suppliers are an integral part of the supply chain and, therefore, the process of production and delivery should by understood and supplier relationships developed and improved. Supplier failures can increase the cost of poor quality through excess inventory, downtime, additional testing, and customer satisfaction. On the other hand, a significant strategic advantage can be gained by excellent supplier management. One of the seven quality principles of ISO 9001 is to build relationships with suppliers because it is a critical component of sustained success.
Contact:
Tél.: [18887172436];     Email.: referral@complianceonline.com
Sujets:
Supplier, and, Contract, Manufacturer, Management, ComplianceOnline
Identifiant de l'évènement:
1329309
4
Change Management System
07 avr 2020 • online, États-Unis
Organisateur:
Compliance4all
Contact:
Netzealous LLC,DBA -Compliance4all;     Tél.: [8004479407];     Email.: support@compliance4All.com
Sujets:
Control Management, Management Systems, FDA, Validation Systems
Identifiant de l'évènement:
1333692
Sujets apparentés:
5
Implementing an Effective CAPA System
10 avr 2020 • online, États-Unis
Organisateur:
Compliance4all
Contact:
Netzealous LLC,DBA -Compliance4all;     Tél.: [8004479407];     Email.: support@compliance4All.com
Sujets:
Quality Management System, CAPA, Root Cause Analysis, FDA, Online Training
Identifiant de l'évènement:
1333702
Sujets apparentés:
6
FDA's Problem with Software Monsters
13 avr 2020 • online, États-Unis
Organisateur:
Compliance4all
Contact:
Netzealous LLC,DBA -Compliance4all;     Tél.: [8004479407];     Email.: support@compliance4All.com
Sujets:
FDA Guide Lines, Malware Protection, Compliance Training, Learn about Ransomware
Identifiant de l'évènement:
1333744
Sujets apparentés:
7
Hospital Medicine 2020 — SHM's Annual Conference
15 avr 2020 - 18 avr 2020 • San Diego, Californie, États-Unis
Organisateur:
Society of Hospital Medicine
Résumé:
The SHM Annual Conference is created By Hospitalists, For Hospitalists. and is the “fastest growing conference in healthcare” with thousands of attendees every year and can help put hospitalists' careers on the fast track.
Identifiant de l'évènement:
1247869
Sujets apparentés:
8
WIN — 20/20 and Beyond: Envisioning the Future of Nursing Research, Practice, and Education
15 avr 2020 - 18 avr 2020 • Portland, Oregon, États-Unis
Résumé:
The Western Institute of Nursing (WIN) is an organization that addresses the needs and interests of nurses and students engaged in research, practice, and education in all areas of health care. WIN invites you to submit an abstract in research, project, or methodology and/or theory development/conceptual format to be considered for podium or poster presentation at the 2020 WIN Conference in Portland, Oregon, April 15-18. Papers must be completed by the abstract submission deadline to be eligible for podium presentation either as individual papers or as part of a symposium. In-progress research or projects are eligible for poster presentation. Completed research, projects, and theory development /conceptual papers are also eligible for poster presentation. All abstracts, not to exceed 500 words, are to be submitted using WIN’s abstract submission form. Submissions must be received by 11:59 PM Pacific time on Tuesday, October 15, 2019.
Contact:
Tél.: [503/494-0869];     Email.: win@ohsu.edu
Sujets:
Nursing Research, Nursing Education, Clinical Practice, Public Health
Identifiant de l'évènement:
1261418
Sujets apparentés:
9
Quality Control Laboratory Compliance - cGMPs and GLPs
16 avr 2020 - 17 avr 2020 • Boston, MA, États-Unis
Organisateur:
Complianceonline
Résumé:
FDA inspection and oversight of quality control (QC) laboratories are essential elements of the agency’s evaluation of the compliance status of regulated companies representing multiple industries - pharmaceuticals, biologics, medical devices, as well as foods and cosmetics - as well as the contract QC laboratories which service these industries. Lack of compliance can result in severe regulatory actions, criminal liability, fines, and the inability to obtain product approvals.
Contact:
Tél.: [18887172436];     Email.: referral@complianceonline.com
Sujets:
Quality Control Lab regulations, QC Lab regulations, FDA QC Lab requirements, FDA lab regulations, Good Laboratory Practices, GLP, cGMP, Current Good Manufacturing Practices, Lab compliance training, laboratory regulations, lab compliance, quality control laboratory, stability studies, laboratory instruments, laboratory supplies, laboratory investigations
Identifiant de l'évènement:
1324656
10
How to Mitigate Microbials in Purified Water and WFI Water Systems: Theory and Practical Application Details Thoroughly Explained Clearly and Concisely
16 avr 2020 - 17 avr 2020 • Newark, NJ, États-Unis
Organisateur:
Complianceonline
Résumé:
This course is a comprehensive training on pharmaceutical water systems encompassing over 15 different course subject and modules. The modules include design, build, installation, validation, regulatory compliance, regulatory audit expectations, documentation expectations, modules on continuous electrodeionization (CEDI), ozone, reverse osmosis (RO), distillation methods, pure steam generation, pretreatment options, microbial mitigation and sanitization methods, raw water and sourced water criteria, instrumentation for both observational and compendial criteria, and automation expectations.
Contact:
Tél.: [18887172436];     Email.: referral@complianceonline.com
Sujets:
pharmaceutical water system, pharmaceutical water testing, pharmaceutical water system design, pharmaceutical water system validation, pharmaceutical water sampling, pharmaceutical water system compliance, pharmaceutical water system training, water for injection paradigm, water system training, microbial monitoring, microbial mitigation, pharmaceutical water systems sanitization methods, pharmaceutical water production, pharmaceutical water system compendial criteria
Identifiant de l'évènement:
1329182
11
Beyond NanoEHS Risk Assessments - Leading at the Interface of Science and Business
20 avr 2020 - 21 avr 2020 • Orlando, FL, États-Unis
Organisateur:
Complianceonline
Résumé:
Responsible commercialization of new technologies requires leadership at the interface of science and business. For example, advances in materials and applications require a constant attention to the potential risks for the environment, health, and safety (EHS). The development of nanomaterials over the last fifteen years serves as a useful example of a framework for responsibly commercializing new technologies. This course will provide an overview of how to use a tiered-approach framework for identify and mitigating potential risks during the R&D and product development cycle, while also improving the leadership skills required to develop a culture focused on success.
Contact:
Tél.: [18887172436];     Email.: referral@complianceonline.com
Sujets:
"NanoEHS Risk Assessments, NanoEHS, nanomaterial environmental health and safety, advanced material science instrumentation, advanced materials research, measuring nanomaterials
Identifiant de l'évènement:
1329214
12
Building a Vendor Qualification Program for FDA Regulated Industries
20 avr 2020 - 21 avr 2020 • Orlando, FL, États-Unis
Organisateur:
Complianceonline
Résumé:
This course will provide detailed explanations and examples for Building a Vendor Qualification Program for FDA Regulated Industry. With today’s pharmaceutical market, raw materials, Active Pharmaceutical Ingredients (API), Containers & Closures, inactive or excipients and other components are being sourced from all over the world. We also have Third Party Manufacturers and outside testing facilities that are part of our supply chains. Building and following a robust vendor qualification Program is essential for pharmaceutical and chemical manufacturers. We must create a procedure, which will be used to remain aware of the compliance status for all of our suppliers. Some raw material components may move from producers to brokers to the end users. In addition, there may be other shippers and wholesalers responsible for moving and holding our raw material components.
Contact:
Tél.: [18887172436];     Email.: referral@complianceonline.com
Sujets:
Vendor qualification program, vendor requirements, off-site audit checklist, on-site verification form, vendor qualification, basics of quality system, FDA regulations
Identifiant de l'évènement:
1329242
13
NHC 2020 — 2020 NURSING EDUCATION, NURSING AND HEALTHCARE CONFERENCE
22 avr 2020 - 23 avr 2020 • Houston, États-Unis
Organisateur:
Innovinc International
Résumé:
2020 Nursing and Healthcare (NHC-2020) provide invaluable opportunities to extend and strengthen the Nursing and Healthcarecommunity, and our collective body of knowledge.
Contact:
Tél.: [14083521010];     Email.: maryjane@nhc2020.com
Sujets:
Nurse Education, Health Care Systems, Nursing & Healthcare Management, Epidemiology and Public Health, Trauma, Critical Care, Nursing Practice & Safety, Disease Transmission and Outbreak, The Changing role of Modern Nursing, Nursing Leadership, Midwifery Nursing & Women's Health, Pain Management & Preventive Medicine, Improving Patient Education, Care & Outcomes, Nursing Informatics & Technology, Palliative Care & Improving Medication Safety, Advances in Nursing, Primary Care & Administration, Evidence-Based Nursing, Healthcare Informatics Research, Child and Adolescent Mental Health, Globalization and Health, Public Health & Safety, Occupational and Health Safety.
Identifiant de l'évènement:
1305804
14
Latin America – Understanding Regulatory Compliance Requirements Across the Life Science Industry (Pharmaceuticals, Biologics, Medical Devices, IVDs)
23 avr 2020 - 24 avr 2020 • San Diego, Californie, États-Unis
Organisateur:
Complianceonline
Résumé:
The Latin America Regulatory compliance requirement training/seminar will cover topics across the full Life-Cycle of Company & Product licensing in the key markets of Latin America. Written Regulations vs. Skillful Negotiation will be explained across every critical topic. The importance of local resources, Agency meetings and knowing how to navigate the regulatory landscape will accelerate country establishment and successful product licensing.
Contact:
Tél.: [18887172436];     Email.: referral@complianceonline.com
Sujets:
Latin America regulations, Latin America life sciences regulations, Latam life sciences regulatory requirements, Latin America pharmaceutical regulations, Latin America medical device regulations, Latin America biologics regulations, Argentina life sciences regulations, Argentina medical device regulations, Argentina biologics regulations, Brazil life sciences regulations, Brazil medical device regulations, Brazil biologics regulations, Mexico life sciences regulations, Mexico medical device regulations, Mexico biologics regulations, Latin America clinical requirements, Latin America pre-clinical requirements
Identifiant de l'évènement:
1324591
15
Nursing — Nursing Education, Practice & Nursing management
08 mai 2020 - 09 mai 2020 • Toronto, Canada
Résumé:
It’s a great pleasure to welcome you all to our prestigious Nursing Education, Practice & Nursing management held in TORONTO, CANADA from May 8 and 9, 2020. Nursing Education, Practice & Nursing management is hosted by the International Experts of ICON Events. This International Nursing Conference brings perfect networking platform for experts to share their latest research and advancements in Nursing and associated fields.
Contact:
Tél.: [+1 9492811115];     Email.: Natalieeisenberg378@gmail.com
Sujets:
Nursing Planning, organizing, staffing, directing and controlling Nursing Leadership Health Care Management Nursing Care & Practitioners Nursing Education & Research Community Health Nursing
Identifiant de l'évènement:
1266934
Sujets apparentés:
16
Managing Your Complaints and Obstacles in Post-Market Requirements -- Results from Top Medical Device Observations During an Inspection
14 mai 2020 - 15 mai 2020 • Minneapolis, MN, États-Unis
Organisateur:
Complianceonline
Résumé:
Post-Market activities, Complaint Handling, MDRs, and Recalls are expensive, time consuming, and often lead to more serious financial consequences. Over 80% of FDA Inspection target observations for lack of compliance in these areas.
Contact:
Tél.: [18887172436];     Email.: referral@complianceonline.com
Sujets:
medical device recalls seminar, medical device regulations seminar, medical device reporting, medical device complaint management, medical device complaint handling, MDR, CAPA, risk management process, class 1 recalls, medical device safety, consumer safety, product safety, medical device reliability, medical device recalls 2019, fda medical device recalls, medical device recalls, fda medical device reporting
Identifiant de l'évènement:
1336117
17
Risk Management in Medical Devices Industry
04 jui 2020 - 05 jui 2020 • Boston, MA, États-Unis
Organisateur:
Complianceonline
Résumé:
Risk management is a mandatory and necessary process during the entire device life. Not only will it help to design and maintain devices efficiently, but it also ensures that the device will be as safe as possible and prevents harms to patients, users, and the environment. Like any process that tries to produce repeatable and consistent results, the risk management process must be clearly understood, including the strengths but also the limitations.By attending this seminar you will learn the main elements of ISO 14971, ISO 13485, IEC62304, IEC62366-1/-2, risk management life cycle steps and benefits, and FDA software reviewers' guidance.
Contact:
Tél.: [18887172436];     Email.: referral@complianceonline.com
Sujets:
medical device risk management training, ISO 14971 workshop, ISO 13485, quality system integration, IEC62304, IEC62366-1/-2, risk management life cycle, FDA software reviewers' guidance, SOP framework, risk rating methods, european special requirements, risk management report
Identifiant de l'évènement:
1333836
Sujets apparentés:
18
Ensuring Compliance with Advertising and Promotional Requirements for Drugs and Medical Devices
04 jui 2020 - 05 jui 2020 • Boston, MA, États-Unis
Organisateur:
Complianceonline
Résumé:
Federal regulation of the advertising and promotion of pharmaceuticals and medical devices reflects an aggressive attitude on the part of the regulators that demands, in turn, that industry be keenly aware of the legal and regulatory duties, as well as key recent trends in enforcement activities by the Federal Government. This course will explore in detail what FDA requires of drug and device firms as well as recent current hot buttons in FDA enforcement activity for the advertising arena.
Contact:
Tél.: [18887172436];     Email.: referral@complianceonline.com
Sujets:
FDA training seminar, FTC advertising seminar, advertising drugs, advertising medical devices, promotion drugs, promoting medical devices, FTC advertising rules, FDA marketing rules, False Claims Act, Off-Label Statements, Drugs social media marketing, medical device social media marketing, Rx Drug Advertising, OTC drug advertising
Identifiant de l'évènement:
1336083
19
Validation, Verification and Transfer of Analytical Methods (Understanding and implementing guidelines from FDA/EMA, USP and ICH)
15 jui 2020 - 16 jui 2020 • Amsterdam, Pays-Bas
Organisateur:
Complianceonline
Résumé:
Analytical methods and procedures should be validated to ensure reliability, consistency and accuracy of analytical data. Compendial methods should be verified to demonstrate the suitability of laboratories to successfully run the method and when methods are transferred between laboratories successful transfer should be demonstrated through testing. In case a laboratory wants to use an alternative method instead of a compendial method, equivalency of the alternative method to the compendial method should be demonstrated.
Contact:
Tél.: [18887172436];     Email.: referral@complianceonline.com
Sujets:
Laboratory compliance, Analytical methods, data, procedures, compendial methods, Method validation and transfer, equivalency testing, FDA inspection, SOPs, FDA and EU compliance, documentation, ICH Q2, USP chapters 220, 1200, 1210, 1220, USP, GLP, GCP, GMP, FDA Warning Letters, Part 11, Annex 11, LOD, LOQ, HPLC to UHPLC, INDA, ANDA, NDA submissions, QbD, statistical evaluation, Training by Dr. Ludwig Huber, Analytic Lab workshop by Dr. Huber
Identifiant de l'évènement:
1324695
20
ORAHS 2020 — 46th International Conference on OR applied to Health Service
26 jul 2020 - 31 jul 2020 • Vienne, Autriche
Organisateur:
University of Vienna
Résumé:
ORAHS provides a network for researchers involved in the application of systematic and quantitative analysis in support of planning and management in the health services sector. The meeting is open to anyone with a quantitative background and those who have interest in the subject area.
Identifiant de l'évènement:
1310581
Sujets apparentés:
21
Laboratory Inspection and Auditing
23 sep 2020 • Philadelphia, PA, États-Unis
Organisateur:
Complianceonline
Résumé:
Quality auditing of pharmaceutical quality control laboratories is an important activity for those performing due diligence or monitoring the performance of a sub-contractor. Besides covering GMP regulations affecting pharmaceutical quality control, this one-day course is designed to provide the non-specialist with the necessary knowledge to understand the quality significance and risk associated with different analytical operations.
Contact:
Tél.: [18887172436];     Email.: referral@complianceonline.com
Sujets:
"Lab safety audit checklist, laboratory audit checklist, chemical laboratory audit checklist, pharmaceutical quality assurance, pharmaceutical guidelines for quality assurance, quality control of drugs, gmp guidelines for pharmaceuticals, laboratory inspection
Identifiant de l'évènement:
1324736
22
19. Deutscher Kongress für Versorgungsforschung
30 sep 2020 - 02 oct 2020 • Berlin, Allemagne
Organisateur:
Kongress- und Kulturmanagement GmbH
Résumé:
Versorgungsforschung - Zugang, Qualität und Effizienz: Gesundheitsversorgung international vergleichen und verbessern
Contact:
Kongress- und Kulturmanagement GmbH;     Tél.: [+49 3643 2468-0];     Email.: info@kukm.de
Identifiant de l'évènement:
1336251


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Dernière mise à jour: 27 Février 2020