Refine results

Educations

By specialty

By typology

Educations by city

Educations by country

Distance learning

Events by keywords

List of medical educations - cme : 61 results

Sort by : Date published|Coming soon - Events filter :

	Your event here Add your medical education - cme. Medical meetings, medical conference, medical education, medical symposium, medical training cycle, medical clinical, medical post graduate degree, medical CME, medical seminar, medical colloquy, medical good practice guide. Doctorama to facilitate the management, promotion and referencing your events.
	Cyber Attacks, Beyond Disaster Recovery - 2017 Ref: 25586 Tuesday August 01st, 2017 - Online Overview: Cyber-attacks and breaches dominate the media and are a significant focus of the government. Businesses and financial institutions are faced with the grim reality that a cyber-attack is inevitable. It's not a matter of if an attack will occur, only ... Education: Medicine, Public Health, Pharmacy, Management
	Effective Supplier Qualification Program - 2017 Ref: 25587 Thursday August 03rd, 2017 - Online Overview: FDA considers the supplier as an extension of your operation. You are liable for supplier’s conduct. FDA will deal with your company in case of product failure, especially as related to end user or patient safety concerns. Areas Covered in the ... Education: Pharmacy, Medicine, Management, Public Health
	FDA Legal Writing Skills for Regulatory & Quality Submissions 2017 Ref: 25609 08/03/2017 -> 08/04/2017 - Raleigh, NC^US Regulatory Affairs professionals Quality Assurance professionals Marketing professionals Scientific and Engineering / Product Development ManagersConsultants to any regulated industry Education: Pharmacy, Medicine
	Statistical Methods A Visual Approach 2017 Ref: 25612 08/03/2017 -> 08/04/2017 - Raleigh, NC^US An essential task in any compliance analytics workflow is to not only explore your data visually, but also to communicate your results professionally with graphic displays. Do you have the tools and skills to quickly and thoroughly perform these tasks? This course in data visualization will present Education: Medicine, Pharmacy
	Achieving Compliance Excellence - 2017 Ref: 25588 Friday August 04th, 2017 - Online Overview: We will discuss each of those keys in detail to enhance understanding and to provide the needed information to replicate the approach in your organization. Why should you Attend: Because as much as we try, most regulated industries don't have a set approach for ... Education: Pharmacy, Medicine, Public Health
	Validation Program to a Building from Top to Bottom - 2017 Ref: 25589 Friday August 04th, 2017 - Online Overview: Many more typical questions are now available in this simple to understand, yet detailed training session designed to help manufacturers of FDA regulated products build a sustainable validation program. Why you should attend: How PLC-based systems or laboratory ... Education: Medicine, Management, Public Health, Pharmacy
	FDA Inspection and Respond to 483 & How to Prepare them - 2017 Ref: 25590 Tuesday August 08th, 2017 - Online Overview: In this webinar you will learn about the types of FDA inspections, preparations such as assigning dedicated personnel to specific tasks for the inspection, facility requirements to support the inspection. Why should you Attend: FDA is required to conduct an ... Education: Medicine, Management, Public Health, Pharmacy
	CAPA within a Device Quality System - 2017 Ref: 25591 Wednesday August 09th, 2017 - Online Overview: You’ll learn how to streamline and monitor your process to ensure compliance and improved performance. If your CAPA process needs a CAPA this webinar is for you. Why should you Attend: Corrective and Preventive Action (CAPA) is the cornerstone of a strong Quality ... Education: Medicine, Management, Public Health, Pharmacy
	Environmental Monitoring Program at FDA Regulations - 2017 Ref: 25592 Thursday August 10th, 2017 - Online Overview: Upon completion of this training, you will be able to Describe how Clean room Environmental Monitoring Program fits into the Regulations. Explain the basis of the Four (4) Phases of Clean room transitional monitoring. Why should you Attend: The cost of ... Education: Medicine, Management, Public Health, Pharmacy
	Laboratory-Developed Tests - Medical devices 2017 Ref: 25593 Thursday August 10th, 2017 - Online Overview: This presentation will review the legal definition of medical device, and how it is applied by FDA to in vitro diagnostic tests. It will review the history of FDA interest in LDTs, and will describe the current situation with respect to Laboratory-developed tests. Why ... Education: Medicine, Management, Public Health
	Documenting Software for FDA Submissions 2017 Ref: 25613 08/10/2017 -> 08/11/2017 - District Of Columbia^US When medical device companies consider Agile development methods, they often run into the key criticism that Agile groups produce little to no documentation, and that Agile stands in contradiction to the lifecycle standards outlined in IEC 62304. In fact, those principles - have clear processes for Education: Pharmacy, Medicine
	ISO 14971 Hazard Analysis at Medical Device - 2017 Ref: 25594 Thursday August 17th, 2017 - Online Overview: The US FDA expects that as part of a product development Design Control Program risk management will be conducted. FDA recommends using ISO 14971 as a guide and has accepted it as a recognized standard. Why should you Attend: FDA expects that as part of a ... Education: Medicine, Management, Public Health, Pharmacy
	HIPAA Compliance Requirements for Business Associates 2017 Ref: 25614 08/17/2017 -> 08/18/2017 - Cincinnati, OH^US Compliance Officer HIPAA Privacy Officer HIPAA Security Officer IT StaffOffice ManagersHealth Application ManagersCompanies providing healthcare data analyticsInformation Systems ManagerChief Information OfficerGeneral Counsel/lawyerPractice Management ConsultantsAny Business Associates that Education: Medicine, Pharmacy
	The Challenges of an Effective Change Control Program 2017 Ref: 25615 08/17/2017 -> 08/18/2017 - San Diego^US An effective quality system program, along with several regulatory requirements, includes the documentation and evaluation of changes made to validated equipment, utilities, processes and controlled documents. To control this process, one must have both a defined change control procedure that outlin Education: Medicine, Pharmacy
	Quality Management System ISO 13485- 2017 Ref: 25616 08/17/2017 -> 08/18/2017 - 60176^US The final version of ISO 13485:2016 is now available and companies should be planning their implementation. There are significant changes from the earlier version; they will require major modifications to the Quality Management System (QMS). The new version has better alignment with FDA's QSR, but t Education: Medicine, Pharmacy
	New FDA FSMA Rules on the Sanitary Transportation 2017 Ref: 25617 08/17/2017 -> 08/18/2017 - Raleigh, NC^US Transportation and Logistics food transportation food safety rules are currently being finalized by the U.S. Food and Drug Administration (FDA). Under congressional instructions, the Food Safety Modernization Act Education: Medicine, Pharmacy
	Letters of Credit are issued under the Customs and Practice 2017 Ref: 25595 Tuesday August 22nd, 2017 - Online Overview: Letters of Credit are the primary instruments for assuring payment of goods sold internationally. Letters of Credit are issued under the Uniform Customs and Practice standard and can be negotiated by over 30,000 banks worldwide. Why should you Attend: With financing ... Education: Medicine, Management, Public Health, Pharmacy
	Medical Devices for Risk Management Techniques 2017 Ref: 25596 Tuesday August 22nd, 2017 - Online Overview: This course will help you understand the regulatory requirements, including ISO14971, and how to create processes and procedures to implement them. Why should you Attend: Many companies have even experienced class action law suits because of product quality issues. ... Education: Medicine, Management, Public Health
	Excel Methods - FDA Device Regulations - 2017 Ref: 25597 Wednesday August 23rd, 2017 - Online Overview: FDA regulations cover both the use of workbooks and the creation of electronic records device manufacturers must understand these regulations and their application. The presentation begins with Excel methods to help ensure the spreadsheet produces the results you want. Why ... Education: Medicine, Management, Public Health
	Clinical Trials - Medical Device FDA's Program 2017 Ref: 25598 Thursday August 24th, 2017 - Online Overview: The topic is device clinical trials. This term refers to the use of medical products on/in humans, in order to gain useful knowledge about the product. Why should you Attend: In spite of the long experience device companies have with clinical trials regulations ... Education: Medicine, Management, Public Health
	FDA Scrutiny of Promotion and Advertising Practices 2017 Ref: 25619 08/24/2017 -> 08/25/2017 - Minneapolis, MN^US If you go "off label" with advertising and promotion, FDA's hammer can hit hard and seemingly out of the blue. Advertising and promotion for devices is weak and lacks legal clarity. For drugs, the regulations are prescriptive and guidance documents clamp down on nuances. Marketing and regulatory aff Education: Medicine, Pharmacy
	Lineament analysis and Quality Assurance and Quality Control procedures 2017 Ref: 25620 08/24/2017 -> 08/25/2017 - Cincinnati, OH^US Upon completing this course, participants should: Understand the limitations of the current exploration process Learn to use lineament and satellite interpretation as a way to define where to concentrate their exploration efforts How to implement QA&QC procedures to guarantee the quality of the Education: Medicine, Pharmacy
	HIPAA 2017 Under Trump 2017 Ref: 25621 08/24/2017 -> 08/25/2017 - Tampa, FL^US The secret is - HIPAA Rules are easy and routine to follow - when they are explained step-by-step in plain language. In this seminar Paul Hales will capture your attention with visual presentations, discussion and learning exercises, and show how to find the right rule with the step-by-step procedur Education: Medicine, Pharmacy
	European Regulatory Procedures 2017 Ref: 25622 08/28/2017 -> 08/29/2017 - Opfikon-Glattbrugg^CH EMA has a 20-year track record of ensuring efficacy and safety of human and veterinary medicines across Europe, and promoting research and innovation in the development of medicines. In its first two decades, the Agency recommended the authorization of a total of 975 human and 188 veterinary medicin Education: Medicine, Pharmacy
	FDA Issues and its FDA Data Integrity - 2017 Ref: 25716 Friday September 01st, 2017 - Online Overview: Many of the data integrity issues that plagued the US drug and biologics industry were eliminated by detailed regulations and stricter enforcement, but many of the problems have resurfaced in recent years among the multitude of foreign manufacturers whoare not familiar with US ... Education: Medicine, Pharmacy, General medicine

Display 25 | 50 | 100 | 200 per page

Page 1/3

1 | 2 | 3

My account	Typology	Events	Support
Login	Academic degree Meeting	Add your events	Site map
Create an account	Conference Seminar	Our references	Help - Frequent asked questions
Forgotten password	Congress Session	Universities - Corporate customers	Contact us
Add Doctorama to your favorites	Medical Education Symposium		About us

Community	Widgets	Partnership	Information
Follow us on Facebook	Import or export a calendar	Improve your search engine rankings	Privacy policy
Follow us on Twitter	Links to events	Press & Professional Websites	Legal Notices
Doctorama by RSS			Terms of Service
Recommend Doctorama
Doctorama.com for Mobile