Medical meetings - Medical educations

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 ...

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 ...

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. ...

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 ...

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 ...

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 ...

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 ...

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 ...

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 ...

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 ...

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 ...

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 ...

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 ...

Complaints, Adverse Event Reporting, and Recalls 2017

Ref: 25496 07/27/2017 -> 07/28/2017 - Distance education

Complaints, Adverse Event Reporting, and Recalls 2017

Overview of Employment Related Risk Management and HR Audits 2017

Ref: 25495 07/27/2017 -> 07/28/2017 - Distance education

Overview of Employment Related Risk Management and HR Audits 2017

HIPAA Security Policies and Procedures an Audits 2017

Ref: 25494 07/27/2017 -> 07/28/2017 - Distance education

HIPAA Security Policies and Procedures an Audits 2017

Laboratory, Medical and Device Performance and Regulatory and Statistical 2017

Ref: 25493 07/27/2017 -> 07/28/2017 - Distance education

Laboratory, Medical and Device Performance and Regulatory and Statistical 2017

Training and Development in the Life Sciences and Regulatory Compliance 2017

Ref: 25492 07/27/2017 -> 07/28/2017 - Distance education

Training and Development in the Life Sciences and Regulatory Compliance 2017

FDA Process Validation for Applied Statistics 2017

Ref: 25491 07/20/2017 -> 07/21/2017 - Distance education

FDA Process Validation for Applied Statistics 2017

Leadership Management Academy 2017

Ref: 25490 07/20/2017 -> 07/21/2017 - Distance education

Leadership Management Academy 2017

ISO14971- Risk Management and Quality System Integration 2017

Ref: 25489 07/20/2017 -> 07/21/2017 - Distance education

ISO14971- Risk Management and Quality System Integration 2017

Statistics for the Non-Statistician 2017

Ref: 25488 07/20/2017 -> 07/21/2017 - Distance education

Statistics for the Non-Statistician 2017

Human Factors Methods and Device Product Life Cycle 2017

Ref: 25487 07/20/2017 -> 07/21/2017 - Distance education

Human Factors Methods and Device Product Life Cycle 2017

Six Steps in Master HIPAA Compliance 2017

Ref: 25486 07/20/2017 -> 07/21/2017 - Distance education

Master HIPAA Compliance in Six Steps

Statistical Process Control -Verification, Validation, Risk Management, Manufacturing, and QA/QC 2017

Ref: 25485 07/13/2017 -> 07/14/2017 - Distance education

Statistical Process Control -Verification, Validation, Risk Management, Manufacturing, and QA/QC 2017