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HIPAA - How Business Associates Can Comply Calmly, Confidently and Completely 2017

HIPAA Rules are easy to follow, step-by-step, once you know the steps. In this seminar Paul Hales will capture your attention with visual presentations, exercises and discussion that explain HIPAA compliance in plain language

  • 10 Days ago
  • 19 Views
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Applied Statistics, with Emphasis on Risk Management in R&D, QA/QC, and Manufacturing 2017

The 2-day seminar explains how to apply statistics to manage risks and verify/validate processes in R&D, QA/QC, and Manufacturing, with examples derived mainly from the medical device design/manufacturing industry.

  • 10 Days ago
  • 18 Views
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FDA's Latest Regulations for Computer Systems Used in the Tobacco and Related Industries, Effective 08/08/2016

FDA Tobacco Control Act Extension of FDA oversight to Vapor, e-Cigarette, Cigar and other industries Details of the August 8, 2016 FDA "Deeming" Regulation Pre-Marketing Tobacco Application (PMTA) Submission FDA Oversight and Compliance Strategy Computer System Validation (CSV) and the System Development Life Cycle Methodology (SDLC) Cost vs. Compliance Policies and Procedures Leveraging Vendors Industry Best Practices FDA Trends

  • 10 Days ago
  • 21 Views
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Drug dissolution testing and establishing plasma drug levels in humans 2017

Drug dissolution testing is an essential and critical step for appropriate and efficient product development such as tablet and capsule. A number of approaches are used to conduct dissolution testing using different apparatuses and methods. Making a choice for an appropriate apparatus and method has always been confusing and challenging.

  • 10 Days ago
  • 19 Views
  • 0 Comments
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Applied Statistics for Scientists and Engineers 2017

Throughout 21 CFR and guidance documents for the pharmaceutical, biopharmaceutical, and medical device industries, the application of statistical methods are specified for: setting validation criteria and specifications, performing measurement systems analysis

  • 10 Days ago
  • 21 Views
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Regulatory Requirements and Principles for Cleaning Validation 2017

This 2 day course will cover practical guidance on cleaning validation regulatory compliance, in conjunction with, risk-based, reasonable and informed decision making and activity planning.

  • 10 Days ago
  • 23 Views
  • 0 Comments
  • 0 Likes

Using Lineament Analysis in Geological Exploration Seminar

Overview: 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 collected data Why should you attend? We will introduce you to an effective and affordable methodology that identifies ..

  • 1 Years ago
  • 501 Views
  • 156 Comments
  • 1 Likes

Conference on Tougher Import Rules for FDA in 2016

Overview: FDA's and the Customs and Border Patrol Service (CBP) have become increasingly sophisticated and equally demanding in the submission of information and adherence to government procedures. Firm's that fail to understand and properly execute an import and export program find that their shipment is delayed, detained or refused. In 2016 entries must use the Automated Commercial Environment (ACE) entry filing system or face entry refusals a..

  • 1 Years ago
  • 1438 Views
  • 971 Comments
  • 1 Likes

Statistics for the Non-Statistician Seminar

Overview:   Statistical tools and techniques are very commonly used to help measure and improve the quality of a firm's process and product. If statistical analysis is not properly performed and/or understood, a firm can run the risk of distributing the kind of product to the market that ultimately fails, resulting in lost time and money. And of course, with statistics, practice makes perfect. During this two-day HIGHLY interactive training p..

  • 1 Years ago
  • 1826 Views
  • 1313 Comments
  • 1 Likes

Seminar on Cleaning Validation Regulatory Requirements and Principles

Course "Regulatory Requirements and Principles for Cleaning Validation" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: This 2 day course will cover practical guidance on cleaning validation regulatory compliance, in conjunction with, risk-based, reasonable and informed decision making and activity planning. This two day interactive course will cover fu..

  • 1 Years ago
  • 985 Views
  • 647 Comments
  • 1 Likes