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466 results of "Life Sciences x"
Live Webinar

Acceptance Sampling for Process Validation and Production Lot Monitoring

Personnel involved in process validation and production control often rely on sampling methods to determine the suitability of a process before moving to production (process validation) or for checking production lots for acceptance. This webinar provides deta ...

Live Webinar

Excel Spreadsheets; Ensuring Data Integrity and 21 CFR Part 11 Compliance

This interactive webinar explains how to configure and validate a GxP compliant spreadsheet applications to avoid FDA 483s. Follow the step-by-step instructions as we configure Excel for audit trails, security features, and data entry verification. Understand ...

Live Webinar

Stability Studies and Estimating Shelf Life with Regression Models

Manufacturers of foods, drugs, consumer goods, and other products must determine the shelf life of their products so that customers know when the product can be expected to perform as intended. Many approaches are available to quantify the "shelf life" and the ...

Live Webinar

Technical Documentation with the new Medical Device Regulation EU MDR 745/2017

The STED-File with the special format as technical documentation covers a lot of countries and helps to have technical documentation in global acting companies. A STED-File collect all the data’s and can help you to keep the overview to deal with this format r ...

Live Webinar

Supply Chain Security Procedures and Training to Support Customs and Trade Partnership Against Terrorism (C-TPAT) Compliance

The market for counterfeit and contraband, or “pirated” products can be divided into two important areas. The primary market provides consumers with counterfeit and contraband products. These consumers believe they have purchased genuine products. However, the ...

Live Webinar

The Human Error Tool Box: A Practical Approach to Human Error

Human error is known to be the primary cause of quality and production losses in many industries. Although it is unlikely that human error will ever be eliminated, many human performance problems can be prevented. Human errors start at the design stage. From p ...

Live Webinar

Implementation and Management of GMP Data Integrity

Data integrity is the assurance that data records are accurate, complete, intact and maintained within their original context, including their relationship to other data records. This definition applies to data recorded in electronic and paper formats or a hyb ...

Live Webinar

Pharmaceutical Compressed Air: Quality GMP Standards and Requirements

Compressed air for pharmaceutical use is considered a critical utility as many of its applications involve direct contact with the pharmaceutical product. The design, construction, and monitoring of a compressed air system are essential for maintaining a quali ...

Live Webinar

Four Simple Key Performance Indicators for Continual Improvement

Poor quality is only one of the Toyota production system's Seven Wastes, and it is also the only one that announces its presence. The other six are (1) asymptomatic, (2) often present 100% of the time because they do nothing to announce their presence, and (3) ...

Live Webinar

The 6 Most Common Problems in FDA Software Validation and Verification

This training on FDA software validation and verification will provide you the best practices necessary to ensure that all systems are validated in compliance with FDA regulations.