World Conference Calendar

33622 Conferences

Health and Medicinerss


BIT's 3rd Annual International Congress of Antibody  (ica2011)

BIT's 3rd Annual International Congress of Antibody (ica2011)

Location: , China
Category: Health and Medicine
Start Date: 03-23-2011 Last Day: 03-25-2011
Dear Friends and Colleagues, BIT Life Sciences is proud to announce that the 3rd Annual International Congress of Antibodies (ICA-2011) will be held March 23-25, 2011 in Beijing, China with the theme “Discovery, Partnering to Market.” On behalf of the organizing committee, I cordially invite you to attend our conference. Initiated by BIT Life Sciences in 2008, ICA offers a unique meeting place for professionals from all over the world to share scientific information, seek research collaborations, foster new business opportunities, and discuss how to prevent and treat disease. In 2010, ICA was held with the 2nd Annual World Vaccine…
BIT's 3rd Annual World Vaccine Congress  (wcv2011)

BIT's 3rd Annual World Vaccine Congress (wcv2011)

Location: , China
Category: Health and Medicine
Start Date: 03-23-2011 Last Day: 03-25-2011
Dear Friends and Colleges, BIT Life Sciences is proud to announce that the 3rd Annual World Vaccine Congress (WCV-2011) will be held in Beijing China with the theme “The Future of Global Vaccines.” WCV-2011 will be the largest meeting devoted exclusively to research of vaccines associated with infectious and non-infectious diseases in China. The meeting will gather experts from all over the world to discuss exciting breakthroughs and to share information on emerging vaccine technologies. To protect the world from health threats, we need a safe and effective supply of vaccines urgently. BIT Life Sciences’ Annual World Congress of Vaccine…
Meet FDA Expectations for a Tougher Supplier Audit Program - Webinar By GlobalCompliancePanel

Meet FDA Expectations for a Tougher Supplier Audit Program - Webinar By GlobalCompliancePanel

Location: , United States
Category: Health and Medicine
Start Date: 03-23-2011 Last Day: 03-23-2011
Overview: There is a pervasive public perception that the FDA has been ineffective in protecting the public. Recent news events seem to support this perception. The FDA is working hard to change that perception. Industry must be prepared to adapt, and recognize that such adaptation will actually work to their long-term benefit. This webinar will discuss and evaluate the effects that this call for change has on a company and its selection, audit, use and on-going relations with its suppliers of services and products / components. How can companies address the FDA's stated desire to require "on-site" audit of all…
FDA's New Process Validation Guidance - Webinar By GlobalCompliancePanel

FDA's New Process Validation Guidance - Webinar By GlobalCompliancePanel

Location: , United States
Category: Health and Medicine
Start Date: 03-23-2011 Last Day: 03-23-2011
Overview: Nearly two years after releasing a draft validation guidance to replace their antiquated General Principles of Process Validation (1987), in January 2011 FDA finally published the official standard. While technically"guidance," FDA has indicated they will enforce compliance rigorously. This complete overhaul of FDA's primary validation standard brings U.S. drug. API, and biologics process validation up to par with the advanced and modern expectations of European authorities and CDER's sister medical device division. The new requirements expand validation from a one-time activity into a full lifecycle philosophy, encompassing statistics, risk management, project management, and new technologies. No one involved in…
Validation of Existing/Legacy Computer Systems for FDA/EU Compliance - Webinar By GlobalCompliancePanel

Validation of Existing/Legacy Computer Systems for FDA/EU Compliance - Webinar By GlobalCompliancePanel

Location: , United States
Category: Health and Medicine
Start Date: 03-23-2011 Last Day: 03-23-2011
Overview: When existing or legacy computer systems are used in FDA or equivalent international environments they should be validated, a process sometimes called retrospective validation. While the industry is very well familiar with the validation of new systems, there are many questions about existing or legacy systems. This web seminar will give a good understanding on the regulatory requirements, and it will have recommendations and provide tools for effective implementation. Reference material for easy implementation: * SOP: Retrospective Validation of Computerized Systems * Checklist: Retrospective Validation of Computer Systems Areas Covered in the Session: * Definition of legacy systems and…
Codependency

Codependency

Location: , United States
Category: Health and Medicine
Start Date: 03-22-2011 Last Day: 03-22-2011
"Codependency" will be presented on Tuesday March 22, 2011, from 7:30 pm to 9:00 pm; by Ronald E. Harrison; Chemical Dependency Therapist. This program will discuss the symptoms and progression of codependency and describe actions and resources that help codependent people to recover from codependency. This program is part of the FREE, annual Dawn Farm Education Series. Our presentations offer helpful information that supports chemically dependent people in achieving, maintaining, and strengthening their recoveries. The series educates family members on issues relating to addiction and its effect on the family, and offers information that will be useful for friends and…
Medical Device Recalls: How to Manage Them and Recent Trends - Webinar By GlobalCompliancePanel

Medical Device Recalls: How to Manage Them and Recent Trends - Webinar By GlobalCompliancePanel

Location: , United States
Category: Health and Medicine
Start Date: 03-22-2011 Last Day: 03-22-2011
Overview: Medical devices are classified into three classes, Class I, II, and III, based on the level of control necessary to assure the safety and effectiveness of the device. Recalls of Class II devices represent 61% of all device recalls over a review period, followed by Class III devices at 28%. This Webinar will provide a recent update on the latest trends and causes for device recalls and emerging trends. Recall means the correction or removal of a device for human use where FDA finds that there is a reasonable probability that the device would cause serious, adverse health consequences…
Fundamentals of OSHA Injury and Illness Recordkeeping with Key Interpretations

Fundamentals of OSHA Injury and Illness Recordkeeping with Key Interpretations

Location: , United States
Category: Health and Medicine
Start Date: 03-22-2011
This OSHA injury and illness recordkeeping webinar will explain how to determine work relatedness and determine which cases are recordable on the OSHA form 300. It will also explain key and recent OSHA recordkeeping interpretations. Why Should You Attend: Most employers are required to maintain injury and illness records but doing so can be a daunting task due to the challenge of understanding OSHA’s recordkeeping procedures. This easy to follow presentation explains how to determine work relatedness and decide which cases should be recorded on the OSHA form 300. It also explains difficult to understand concepts of recordkeeping such as…
Documentation for IEC 60601-1 3rd Edition Compliance - Webinar By GlobalCompliancePanel

Documentation for IEC 60601-1 3rd Edition Compliance - Webinar By GlobalCompliancePanel

Location: , United States
Category: Health and Medicine
Start Date: 03-22-2011 Last Day: 03-22-2011
Overview: In this presentation we will review the certification requirements for documentation of the clauses of IEC 60601-1 Third Edition. The purpose will be to provide medical device manufacturers with information on how to provide certification bodies with the information they need to certify products to the Third Edition in the most efficient manner. By preparing in advance for certification reviews and testing, the product should move through the process quickly and efficiently. We will especially look at the risk management documentation requirements and how to provide the information requested. Why you should attend: In 2012, IEC 60601-1 3rd Edition…
Introduction to Contamination Control Master Plans - Webinar by GlobalCompliancePanel

Introduction to Contamination Control Master Plans - Webinar by GlobalCompliancePanel

Location: , United States
Category: Health and Medicine
Start Date: 03-17-2011 Last Day: 03-17-2011
Overview: This webinar concentrates on the value of creating a master plan for contamination risks within a GMP manufacturing company. It provides an introduction to the creation, implementation, and maintenance of a Contamination Control Master Plan. Key benefits of this seminar include: * Achieve satisfactory inspections more easily * Higher assurance of new medical product approvals * Minimize nonconformances * Reduce rates of batch rework and rejections * Avoid product recalls * Identify and control the key contamination concerns for your company * Take a holistic approach to contamination control * Achieve synergy among control programs Why you should attend:…
How to use QSIT to Your Advantage - Webinar By GlobalCompliancePanel

How to use QSIT to Your Advantage - Webinar By GlobalCompliancePanel

Location: , United States
Category: Health and Medicine
Start Date: 03-17-2011 Last Day: 03-17-2011
Overview: Virtually all field inspections performed by FDA inspectors are done according to the QSIT. It is thus imperative that all regulated companies have an in-depth knowledge of this system, to enable them to prepare for the inspection. Delving into each and every section of the QSIT, this webinar also includes straightforward, helpful methods for incorporating it into your company’s ongoing quality system. Why you should attend: If you don't know what the FDA inspector is going to look at when (s)he performs his/her audit, how can you really know what to prepare for? Even a thorough internal audit may…
Regulatory Complaint Handling, Vigilance & Recalls - Webinar By GlobalCompliancePanel

Regulatory Complaint Handling, Vigilance & Recalls - Webinar By GlobalCompliancePanel

Location: , United States
Category: Health and Medicine
Start Date: 03-17-2011 Last Day: 03-17-2011
Overview: Improper complaint handling can result is serious regulatory problems as well as hitting the bottom line. Recalls, FDA Warning letters & even seizures could result. This presentation will review the regulatory requirements for complaint handling and adverse events reporting in the USA, EU & Canada. Suggestions for investigating and documenting complaints & pitfalls will be included. Areas Covered in the Session: * Complaints Definitions; FDA, EU & Canada * How to Document Complaints & Adverse Events * US & Foreign Regulatory Reporting * Recall, Vigilance, Correction & Removals * Enforcement Actions Who Will Benefit: * Regulatory Professionals * Quality…
Efficient Computer System Validation - 10 Easy Steps - Webinar By GlobalCompliancePanel

Efficient Computer System Validation - 10 Easy Steps - Webinar By GlobalCompliancePanel

Location: , United States
Category: Health and Medicine
Start Date: 03-16-2011 Last Day: 03-16-2011
Overview: This webinar details all of the templates used to create validation documentation, usually saving two-thirds of the time and costs. The 10-step risk-based approach to COTS software validation minimized documentation and ensures efficient implementation of new and upgraded computer systems. This experience will prepare you to perform a validation project. Areas Covered in the Session: * Learn which documents the FDA expects to audit. * How to use the risk-based validation approach to lower costs. * How to link requirements, specifications, risk management, and testing. * Document a computer system validation project using easy to understand fill-in-the-blank templates. *…
Identifying and managing unplanned protocol excursions and adhering to GCP

Identifying and managing unplanned protocol excursions and adhering to GCP

Location: , United States
Category: Health and Medicine
Start Date: 03-16-2011
This webinar will provide practical strategies to minimize and manage protocol deviations and adhere to key elements of Good Clinical Practices. Why Should You Attend: During the implementation and conduct of study protocols, investigators often fail to adhere to many elements of GCP regulations. Such violations can potentially impact patient safety and data integrity as well as increase risks to the subject population. Despite extensive and costly monitoring by sponsoring companies, study audits continue to identify protocol deviations and violations resulting in numerous FDA 483 citations. This presentation will help participants identify key risk elements of protocol non-compliance, understand the…
Relapse Prevention

Relapse Prevention

Location: , United States
Category: Health and Medicine
Start Date: 03-15-2011 Last Day: 03-15-2011
"Relapse Prevention" will be presented on Tuesday March 15, 2011, from 7:30 pm to 9:00 pm; by Robin Edison, M.Ed., LPC, NCC, CAAC; Coordinator, Dawn Farm Downtown program. The relapse process begins before alcohol/other drug use resumes. This program will discuss the dynamics of relapse, the warning signs that lead the chemically dependent person into a relapse, and strategies to prevent relapse and handle high-risk situations. This program is part of the FREE, annual Dawn Farm Education Series. Our presentations offer helpful information that supports chemically dependent people in achieving, maintaining, and strengthening their recoveries. The series educates family members…
Off-Label Promotion of Drugs - Regulatory Documents Explained - Webinar By GlobalCompliancePanel

Off-Label Promotion of Drugs - Regulatory Documents Explained - Webinar By GlobalCompliancePanel

Location: , United States
Category: Health and Medicine
Start Date: 03-15-2011 Last Day: 03-15-2011
Overview: Promoting a drug or device for a use not approved by the Food and Drug Administration is illegal. As a result of this practice, called "off-label promotion," life sciences companies have been fined unprecedented amounts of money and their executives have been prosecuted criminally. In addition to the regulatory and criminal consequences of off-label promotion, companies that promote off-label may be responsible for large plaintiffs' verdicts in products liability cases that arise from the off-label uses of their products. The pharmaceutical industry has been distributing reprints of scientific and journal articles on off-label uses of drugs for many years…
Nuts and Bolts of California Environmental Regulations – Differences between U.S. EPA and State Requirements

Nuts and Bolts of California Environmental Regulations – Differences between U.S. EPA and State Requirements

Location: , United States
Category: Health and Medicine
Start Date: 03-15-2011
This environmental regulation training will explain in details the differences between California Environmental Regulations and U.S. EPA and Other State Requirements. Why Should You Attend: This webinar will explain, in a well-organized and effective manner, the key differences in regulations that any person responsible for environmental compliance in California needs to know. As most national and international corporation headquarters are located outside of California, there often is a gap in understanding this state’s unique, complicated, and heavily-enforced environmental regulations. This is due in part to the fact that most other states consistently follow U.S. EPA environmental regulations, whereas many California…
Bringing Compliance To Design Control For Older Products - Webinar By GlobalCompliancePanel

Bringing Compliance To Design Control For Older Products - Webinar By GlobalCompliancePanel

Location: , United States
Category: Health and Medicine
Start Date: 03-15-2011 Last Day: 03-15-2011
Overview: The webinar examines critical parts of design control after product release including: design change control, design validation, and the Design History File. The webinar is designed to help regulatory Affairs, Quality Engineers, and Design Engineers maintain released products within current regulatory requirements. As an attendee you will learn what the FDAs expectations for your released products are. You will also learn about the paper trail you are required to maintain to show compliance. Compliance regulations are released by regulatory bodies throughout the product's life cycle. It is a requirement for the manufacturer of devices to ensure that the released…
HIPAA Breach Notification: What to do to prevent breaches, and what to do when they happen to you - Webinar By GCPanel

HIPAA Breach Notification: What to do to prevent breaches, and what to do when they happen to you - Webinar By GCPanel

Location: , United States
Category: Health and Medicine
Start Date: 03-15-2011 Last Day: 03-15-2011
Overview: The new HIPAA Breach Notification Rule required by the HITECH Act within the American Recovery and Reinvestment Act of 2009 went into effect September 23, 2009, requiring all HIPAA covered entities and business associates to follow a number of steps to be in compliance. * The HIPAA Breach Notification Rule has been in effect since September 23, 2009 and most organizations are not prepared to respond to a breach of PHI and report and document it properly. We will discuss the origins of the rule and how it works, including interactions with other HIPAA rules and penalties for violations.…
Malaysian Symposium on Biomedical Science 2011

Malaysian Symposium on Biomedical Science 2011

Location: , Malaysia
Category: Health and Medicine
Start Date: 03-12-2011 Last Day: 03-13-2011 Deadline for abstracts: 01-31-2011
Living in this challenging stage of time, our motherland calls for a large number of intellectuals, devoted and skillful person are exceedingly vast. These individuals are the backbone for the development of consecutive model for our swift developing country. For Malaysia, educational affairs are among imperative field of interest. Embolden of scientific thinking among the community has shaped our daily live into an interesting and innovative ways. It will ensure us to narrow our shipping course into a right track en route for a first class intellectual model as well as an aspiration to be more competitive and excellence worldwide…

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