World Conference Calendar

33841 Conferences

Health and Medicinerss


Recalls, Removals, and Market Corrections in Compliance with FDA and ISO Requirements - Webinar By GlobalCompliancePanel

Recalls, Removals, and Market Corrections in Compliance with FDA and ISO Requirements - Webinar By GlobalCompliancePanel

Location: , United States
Category: Health and Medicine
Start Date: 01-13-2011 Last Day: 01-13-2011
Overview: To satisfy QSR and ISO 13485 requirements, medical device companies must respond to field reports swiftly and compliantly. There are certain circumstances in which a report from the field requires the device manufacturer to take steps regarding product in the field. It is critical that the company take the required steps in the required timeframes. FDA and ISO requirements overlap to a great extent, but not completely. This webinar sets forth the requirements for recalls, removals, and market corrections, and provides recommended practices. Why should you attend: There are certain circumstances in which a report from the field requires…
Military Construction Contracting Safety Regulations  OSHA & the EM385-1-1, what you dont know could cost you your contract!

Military Construction Contracting Safety Regulations OSHA & the EM385-1-1, what you dont know could cost you your contract!

Location: , United States
Category: Health and Medicine
Start Date: 01-13-2011
Although the EM 385-1-1 regulations match up well with OSHA 1926, even the experienced safety professional can easily overlook the differences. A business can find them in serious trouble if they arent aware of the differences, facing fines and even loss of a contract. This course will educate those both novices and experienced on those differences, and what you need to do to keep the safety officers off your back, and your money in your wallet. Whether you are the general contractor or a subcontractor, Project Manager, Superintendent, or Safety Officer.this is a vital course you wont want to miss.…
Labeling Requirements for Dietary Supplements - Webinar By GlobalCompliancePanel

Labeling Requirements for Dietary Supplements - Webinar By GlobalCompliancePanel

Location: , United States
Category: Health and Medicine
Start Date: 01-13-2011 Last Day: 01-13-2011
Overview: This webinar points out current labeling issues including misbranding that are eating into profitability of dietary companies. The webinar teaches the attendee how to avoid common labeling compliance issues including: * Misbranding * Misleading claims * Misleading statements * Directions of use The webinar focuses on general labeling provisions for dietary supplements, requirements for inner and outer packaging, and claims made on e-commerce websites. Why should you attend: * Avoid product recalls * Be in compliance with labeling requirements * Avoid wastage in regulatory fines * Improve your profitability Areas Covered in the Session: * Labeling defined * Current…
How to investigate environmental monitoring excursion limits - Webinar By ComplianceOnline

How to investigate environmental monitoring excursion limits - Webinar By ComplianceOnline

Location: , United States
Category: Health and Medicine
Start Date: 01-14-2011
This environmental monitoring training will review the best practices for setting environmental monitoring alert and action levels for viable and non-viable data including product bioburden. In addition this webinar will address the responses/actions that should be taken when an excursion in the alert or action level occurs. Areas Covered in the Seminar: Best practices for monitoring and establishing limits. Product bioburden Viable particulate Non-viable particulate Do I really need to investigate if the alert limits are exceeded? Investigating an alert limit excursion. In the environment On the product Who to investigate. What to investigate. When - what is the appropriate…
Change Control Systems for Medical Devices Current Best Practices for FDA-Compliant Systems - Medical Device Webinar By ComplianceOnline

Change Control Systems for Medical Devices Current Best Practices for FDA-Compliant Systems - Medical Device Webinar By ComplianceOnline

Location: , United States
Category: Health and Medicine
Start Date: 01-18-2011 Last Day: 01-18-2011
This change control training will discuss the best practices to create a FDA compliant system. Areas Covered in the Seminar: QSR requirements for document change control. Description of typical document change control system in use. Streamlined document change control process. Paper-free document review. Immediate document distribution. Paper-free document management system. Document change requests: submission, processing, and review. Document change approval and distribution. How to handle "Minor" changes. Streamlined document change control process. Change control for design documentation. Who Will Benefit: This webinar will provide valuable assistance to all regulated companies that are interested in spending less time on change control.…
Trauma and Chemical Use and Addiction

Trauma and Chemical Use and Addiction

Location: , United States
Category: Health and Medicine
Start Date: 01-18-2011 Last Day: 01-18-2011
"Trauma and Chemical Use and Addiction" will be presented on Tuesday January 18, 2011, from 7:30 pm to 9:00 pm; by Dr. Tana Bridge, Ph.D., LMSW; MSW Program Director, School of Social Work, Eastern Michigan University. Current research highlights the relationship between chemical use, addition and trauma. This presentation by an award-winning trauma expert will review events involved with trauma exposure, trauma specific symptomology, the impact trauma has on the brain and on coping and subsequent substance use, and how to aid individuals struggling with trauma and addiction. This program is part of the FREE, annual Dawn Farm Education Series.…
Statistical Sampling Plans for Audits - Webinar By GlobalCompliancePanel

Statistical Sampling Plans for Audits - Webinar By GlobalCompliancePanel

Location: , United States
Category: Health and Medicine
Start Date: 01-18-2011 Last Day: 01-18-2011
Overview: The purpose of auditing is to identify failures in the system or gross negligence. The real question, "how bad does the system need to be for auditing to work?" This talk will look at statistical distribution for rare events to show that the sample size needs to larger when the systems are better. This is a paradox for most auditors who when a problem is discovered increase their sample size. Most auditing sampling plans are based on either the binomial or normal distribution, though rare events usually follow the Poisson distribution. This talk will show how the Poisson relates…
How to Prevent or Handle Protocol Deviations and Violations to be GCP and Regulatory Compliant? - Webinar By GlobalCompliancePanel

How to Prevent or Handle Protocol Deviations and Violations to be GCP and Regulatory Compliant? - Webinar By GlobalCompliancePanel

Location: , United States
Category: Health and Medicine
Start Date: 01-18-2011 Last Day: 01-18-2011
Overview: This Webinar deals with what happens, and under what circumstances, when the protocol is not followed (PNF) and why this is of particular significance. Covered, will be how a protocol deviation with the least significant effect where there is no substantive effect on the risks to research participants, no substantial effect of the value or integrity of the data, and did not result from willful or knowing misconduct on the part of the investigator is handled. It will be important to see what the FDA regulations and the ICH GCP recommendations are in this regard. Most importantly, when do…
Japan - Regulatory Filing Requirements and Compliance Processes for Life Sciences - Part I and Part II - Webinar By GlobalCompliancePanel

Japan - Regulatory Filing Requirements and Compliance Processes for Life Sciences - Part I and Part II - Webinar By GlobalCompliancePanel

Location: , United States
Category: Health and Medicine
Start Date: 01-18-2011 Last Day: 01-18-2011
Overview: This course specifically focuses on the overall regulatory compliance requirements and procedures for Pharmaceuticals, Medical Devices, Biologics and Combination Products in Japan. The course will cover topics relating to pre-clinical and clinical requirements, as well as, addressing the structure of the regulatory agencies in Japan. Content will also include descriptions of the methods by which regulators in the corresponding agencies process filings and registrations and what is expected in the authorization and dossier maintenance of licensed products. The current regulatory climate will be discussed in depth and several examples will be provided to illustrate effective compliance procedures and techniques.…
Medical Device Tracking: Latest FDA Update and Expectations - Webinar By GlobalCompliancePanel

Medical Device Tracking: Latest FDA Update and Expectations - Webinar By GlobalCompliancePanel

Location: , United States
Category: Health and Medicine
Start Date: 01-19-2011 Last Day: 01-19-2011
Overview: The Food and Drug Administration Modernization Act (FDAMA) requires that manufacturers track certain devices when the agency orders them to do so. Tracking is intended to facilitate notification and recall in the event a device presents a serious risk to health that requires prompt attention. The tracking provisions enacted by SMDA required mandatory tracking even if FDA did not issue an order. Specifically, section 519(e), as added by SMDA, required manufacturers to track if they were registered with FDA under section 510 of the act and engaged in the manufacturer of a device if its failure would be reasonably…
Responding to FDA 483s to avoid warning letters - Webinar By GlobalCompliancePanel

Responding to FDA 483s to avoid warning letters - Webinar By GlobalCompliancePanel

Location: , United States
Category: Health and Medicine
Start Date: 01-19-2011 Last Day: 01-19-2011
Overview: In this presentation, we will review recent medical device manufacturers Warning Letters to determine the inadequacies of responses by manufacturers. After finding the weaknesses in the responses, we will identify those characteristics of an adequate response by manufacturers to avoid a Warning Letter and additional enforcement actions by FDA. All medical device companies preparing for FDA inspections should review the information in this presentation and prepare a plan for response to an FDA-483 before the FDA arrives. There will be insufficient time to react during an inspection and after an FDA investigator leaves a FDA Form 483 to develop…
International Stem Cell Corporation Announces Company Update Conference Call

International Stem Cell Corporation Announces Company Update Conference Call

Location: , United States
Category: Health and Medicine
Start Date: 01-19-2011
International Stem Cell Corporation (OTCBB:ISCO), www.internationalstemcell.com, announced today that its Chairman, Kenneth Aldrich and the CEO of its Lifeline Skin Care subsidiary, Ruslan Semechkin, PhD, will present a Webinar discussion of the State of the Company and its plans for its Skin Care subsidiary on Wednesday, January 19, 2011 at 10:00 a.m. PST. In announcing the event, Mr. Aldrich stressed that its purpose is not to announce any new programs or financial results, but to attempt to provide an overview of events during the past year and offer shareholders a perspective on what to expect in the coming year. The…
Preventive and Corrective Maintenance: Protect your assets, Protect your consumers - Webinar By GlobalCompliancePanel

Preventive and Corrective Maintenance: Protect your assets, Protect your consumers - Webinar By GlobalCompliancePanel

Location: , United States
Category: Health and Medicine
Start Date: 01-20-2011 Last Day: 01-20-2011
Overview: A how to guide to meeting customer expectations of the maintenance function. An overview of industry best practices and a review of some leading software solutions. Why you should attend: Maintenance is often found to present the greatest area of opportunity for improvement in the food safety chain. Lack of control of parts and condition of equipment often contributes foreign material to the product resulting in costly product recoveries. Untimely repairs affect productivity as well as customer order fulfillment. A systematic approach to maintenance is critical to operations, quality and safety. Areas Covered in the Session: * Preventive Maintenance…
Effective Training Practices for FDA Compliance - Webinar By GlobalCompliancePanel

Effective Training Practices for FDA Compliance - Webinar By GlobalCompliancePanel

Location: , United States
Category: Health and Medicine
Start Date: 01-20-2011 Last Day: 01-20-2011
Overview: This presentation will answer some of the frequent questions of new trainers or training managers. These include: worker training requirements, the frequency of training, how do design an effective training program, who is responsible for training, training effectives and training documentation. By examining the GMP expectations on training from different regulatory bodies (from the regulations and citations), attendees will be able to envision what to include in a GMP training program. In addition, an overview of the training system, including types of training planning, will offer considerations to make GMP training more effective. Why you should attend: Regulatory agencies…
Device Master Record & Device History Record  requirements, contents and implementation - Medical Device Webinar By ComplianceOnline

Device Master Record & Device History Record requirements, contents and implementation - Medical Device Webinar By ComplianceOnline

Location: , United States
Category: Health and Medicine
Start Date: 01-20-2011
This webinar explains these requirements from QSR and explains the role of each document type. The webinar uses the QSR preamble to explore FDAs thinking, FDA guidance documents for recommendations, and Warning Letters to help participants learn from other firms experience. This webinar provides the information about contents of the records and lessons for implementation. Learning objectives: State the four major records required in FDAs QSR. Describe the contents of the Design History File (DHF). Explain the source of the Device Master Record (DMR). Describe how the Device History Record (DHR) relates to the DMR. State the required content of…
How to Vet an IRB: Expose and Fix Problems Before They Threaten Your Trial

How to Vet an IRB: Expose and Fix Problems Before They Threaten Your Trial

Location: , United States
Category: Health and Medicine
Start Date: 01-20-2011
Understanding of IRB application components and how to find out and fix problem areas before it threaten your trial to fail. Submitting an IRB application right the first time requires a lot of attention to detail. Once a successful application is approved, it is important to keep up with the continuing requirements/submissions/changes etc. Attend this webinar to learn what the IRB is looking for and how to expose and fix problem before they threaten you trial and learn about the role and responsibilities of an efficient well rounded CRC. Areas Covered in the Seminar: IRB- Purpose, Use, Responsibilities. IRB Application…
Clear as Mud: Obtaining and Marketing Your 510(k) With Today's FDA

Clear as Mud: Obtaining and Marketing Your 510(k) With Today's FDA

Location: , United States
Category: Health and Medicine
Start Date: 01-21-2011
Interactive workshop to ensure you understand how to obtain a 510(k) in today's environment at FDA Friday, January 21, 2011, 9:00 AM Pacific to 5 PM Pacific ComplianceOnline partnered with nationally renowed law firm DuVal & Associates to bring this workshop containing 6 hrs training plus 1.5 hr Q & A program and featuring nationally known regulatory attorneys Mark DuVal and Mark Gardner, who have worked on hundreds of 510(k)s, de novo submissions, PMAs and combination products. They will offer insights on the 510(k) process from submission writing and FDA meetings to commercialization strategies for your device. Conference Details:- Price…
Anatomy of a Medical Device Inspection: From EIR to 483 to Warning Letter - Medical Device Webinar By ComplianceOnline

Anatomy of a Medical Device Inspection: From EIR to 483 to Warning Letter - Medical Device Webinar By ComplianceOnline

Location: , United States
Category: Health and Medicine
Start Date: 01-25-2011 Last Day: 01-25-2011
This Medical device inspection webinar training will teach you A to Z of inspection starting with how to prepare to what to do during inspection, close-out interview, FDAs scope, what documents to show and how to respond to the inspection. Areas Covered in the Seminar: How to prepare for an FDA inspection. Development and contents of an SOP for FDA inspection. Personnel training before inspection. How to behave during an inspection. Limitations of scope of inspection. Response to investigation findings. FDA guidance documents used by their inspectors. Who Will Benefit: This webinar will provide valuable assistance to all companies that…
Chemical Dependency and the Family

Chemical Dependency and the Family

Location: , United States
Category: Health and Medicine
Start Date: 01-25-2011 Last Day: 01-25-2011
"Chemical Dependency and the Family" will be presented on Tuesday January 25, 2011, from 7:30 pm to 9:00 pm; by Nancy J. Quay, LMSW; psychotherapist. This program will provide participants with a basic understanding of how addiction impacts each member of a family. The presenter will describe the roles and behaviors that family members often acquire when living with addiction, ways in which each family member is affected by addiction in the family, and options for family members to obtain help to cope with addiction in the family. This program is part of the FREE, annual Dawn Farm Education Series.…
Key Concepts in Successful Water System Sanitization - Webinar By GlobalCompliancePanel

Key Concepts in Successful Water System Sanitization - Webinar By GlobalCompliancePanel

Location: , United States
Category: Health and Medicine
Start Date: 01-25-2011 Last Day: 01-25-2011
Overview: Though hardly a water system is designed and installed without some capability of sanitization, the system design features, materials of construction, sanitization approach, as well as the frequency of the sanitization process have everything to do with its success. This presentation focuses on the factors that can lead to water system sanitization success as well as failure so that the user can not only devise workable sanitization approaches, but also be able to recognize the early symptoms of a sanitization failure and troubleshoot the process for better optimization. Areas Covered in the Session: * Understand the basic water system…

<< Start < Prev 1 2 3 4 5 6 7 8 9 10 Next > End >>

© 2017 World Conference Calendar. All rights reserved.
About WCC | News | FAQs | Links | Terms and Conditions | Privacy | Contact Us