All Conferences

This training program will review the three keys to success for any bank: marketing, financing, and management. The webinar will also include how to correctly interpret the bank’s financial statements including analyzing key numbers and ratios. Additionally, attendees will be exposed to how a bank’s overall success is measured including the CAMELS rating, Baurer Financial Rating, and Texas Ratio. Furthermore, various bank HR issues and the risk of cyber security threats will be outlined.

This webinar will cover creating of a value-added internal auditing program that is compliant to FDA cGMP/ Quality System Regulation and ISO 13485. It will include how to set up and manage the auditing system as well as how to conduct an internal audit and document the results and any nonconformities. It will discuss the value of a good internal auditing program.

Attend this webinar to learn how to set up and use kanbans, JIT, pull system, and drum-buffer-rope in medical device and biotechnology manufacturing start-up operations. Also attendees will learn elements of lean documents and lean configuration, sterilization lot size, MRP II kanban system and how to use kanbans to track off-site sterilization and external supply chain suppliers.

This webinar will explain what money laundering is, various types of money laundering including structuring, micro-structuring and cuckoo smurfing. Attendees will learn how to identify the red flags of money laundering in an account within your institution.

This webinar will take you through the primary sources of compressed air contamination. It will also detail GMP standards and requirements pertaining to compressed air quality.

Chief Customer Officers and Influencers (CCOI), Fall returns this October with more fantastic discussions, knowledge sharing, and networking for the customer-obsessed executive! When we were conducting the research for CCOI Fall, 2019 there was one clear desire that was present on each call; to possess a holistic view of the Customer. Silos come up in every industry and role – they do not discriminate; whether that originates from the CCO’s own team, or the company as a whole. With this holistic theme in mind, we have chosen to divide the agenda into three dominant sections. This has been done to…

OVERVIEW Anyone who’s been a manager will tell you that there is a huge difference between doing and managing. • Instead of doing the work you love, you spend your time in meetings, filling out forms, writing projections and dealing with personnel problems. • Instead of just making sure you get to work at 8:00 AM, you now worry that your team gets there at 8:00 AM. • Instead of worrying about whether your work is sufficiently done and turned in on time, you must worry that your team is sufficiently doing their work and turning it in on time.…

OVERVIEW Bad attitudes, jealousy and disruptive behavior will sabotage hospital morale, lower self-esteem and reduce teamwork and productivity. When toxic behavior infects a department, managers may be tempted to ignore it or give in, the wrong thing to do, but tolerating it is not a solution! This session will show you how to neutralize gossip and put a system in place to ensure it does not re-occur, starting with that of Zero Tolerance and workplace reprimands. The destructive effects of blaming others, griping, pessimism and of always passing the buck needs to be stopped. In this session, you will learn…

Der Allgemeinmedizin Refresher findet vom 08. - 11. Mai 2019 in Hamburg statt. Mit über 5.000 teilnehmenden Ärzten zählen unsere Fortbildungen im Bereich Allgemeinmedizin und Innere Medizin zu den beliebtesten Kursen im deutschsprachigen Raum. In kurzen, 30 – 40 minütigen Blöcken werden die neuesten diagnostischen und therapeutischen Leitlinien der Allgemeinmedizin von Spezialisten präsentiert und auf Ihre Fragen eingegangen. Dabei wird vor allem auf Praxisrelevanz und Didaktik großen Wert gelegt. Unsere Referenten sind Experten in ihren Fachbereichen mit langjähriger Erfahrung in ihrem Betätigungsfeld.

The FDA and other Health Authorities worldwide have focused their attention on data integrity, considering data integrity to be a significant risk to public safety. This is evident in the number of Warning Letter observations and related Import Alerts issued in the last 5-7 years. Data integrity is not a new topic, however, but is a part of the GMPs. Often, companies attempt to address data integrity issues procedurally and by conducting numerous training programs. These tend to be ineffective as data integrity issues are often rooted in a company's culture and may be very difficult to address. Topics covered…

Statistics is a useful decision-making tool in the clinical research arena. When working in a field where a p-value can determine the next steps on development of a drug or procedure, it is imperative that decision makers understand the theory and application of statistics. Many statistical softwares are now available to professionals. However, these softwares were developed for statisticians and can often be daunting to non-statisticians. How do you know if you are pressing the right key, let alone performing the best test? This seminar provides a non-mathematical introduction to biostatistics and is designed for non-statisticians. And it will benefit…

This two-day comprehensive Course on Latin America Regulatory compliance requirements will cover topics ranging from pre-clinical and clinical requirements through product registration, amendments and renewals across Pharmaceuticals, Biologics, Medical Devices and Combination Products. The Course will address the structure of the regulatory agencies in Latin America and discuss local cultural nuances to help you be successful in working with the regulators.

Publication: Accepted papers will be published in the ICTTE proceedings, and submitted for EI Compendex, Scopus, Thomson Reuters (WoS), Inspec index, et al. ++ Submission Methods: Full Paper (publication and oral presentation) Abstract (oral presentation only) Electronic Submission System (.pdf) http://confsys.iconf.org/submission/mepe2019

Publication: Accepted papers will be published in the volume of MATEC Web of Conferences and submitted for Ei Compendex, etc. ++ Submission Methods: Full Paper(publication and oral presentation) Abstract(oral presentation only) Please log in the Electronic Submission System ( .pdf only) to submit your paper. http://confsys.iconf.org/submission/ictte2019 Or, submit your paper via email "[email protected]"

This program will cover the requirements for laboratory controls under US GMP regulations and compare them to those applied by other international health regulatory authorities. Laboratory controls relating to equipment calibration and preventive maintenance; sample chain of custody; good documentation practices; investigation of out of specification and out of trend results; analytical method validation; change control; impact of staffing levels and work flow patterns in the lab on GMP compliance; training and other issues will be included under laboratory controls. The program will also examine the impact of the benchmark court ruling in US versus Barr Laboratories on QC laboratory…

Publication: Accepted and selected papers will be recommended to be published in the International Conference Proceedings Series by ACM (978-1-4503-7623-5), which could be submitted for Ei Compendex and Scopus Index. ++ Submission Methods: Full Paper (publication and oral presentation) Abstract (oral presentation only) Electronic Submission System (.pdf) http://confsys.iconf.org/submission/waie2019 or send your paper via email to "[email protected]"

Publication: All papers of ITET 2019 will be published in International Journal of Information and Education Technology (ISSN: 2010-3689); Abstracting/ Indexing: Scopus (Since 2019), EI (INSPEC, IET), Electronic Journals Library, Google Scholar, Crossref, etc. ++ Submission Methods: Full Paper (publication and oral presentation) Abstract (oral presentation only) Electronic Submission System (.pdf) http://confsys.iconf.org/submission/itet2019

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. This course will examine the fundamental requirements for all QC laboratories subject to FDA inspection, recent trends from FDA inspection reports and enforcement actions. In addition, this course will include a list…

Performing a corporate wide Risk Assessment can seem like a daunting task for an organization. In reality, it can be done using a template and brainstorming with internal auditors, certified fraud examiners and business unit leaders throughout your organization. Understanding your Company's Risk Environment is key to having an effective Internal Audit organization, it helps to have significant experience in internal auditing and a mind for coming up with "what could go wrong" in any control environment. The corporate wide risk assessment can be performed to maximize the efficiency and effectiveness of any organization with a diligent template and process…

If you work in the GMP regulated industry you not only need to address human error deviations because they are an inconvenience, you must do it because the regulation requires it. This training will provide you with the steps required to help you implement a Human Error Reduction Program at your site. It includes practical tools, and how to measure effectiveness to continuously improve human reliability at your site. The CFR - Code of Federal Regulations Title 21 Subpart B_Organization and Personnel Sec. 211.22 talks about the “Responsibilities of quality control unit.” and it states that “(a) There shall be…