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May 14-15 This 2 day seminar will go into the specifics of the REACH and RoHS regulations
Latest FDA Regulatory Requirements & Most Common GMP Issues Caused by Human Error
MP3 Download this training would provide tools that can be implemented and used after this event.
MP3 Download This is a one (1) day training course on the Toxic Substance Control Act and the latest developments for 2023
MP3 Download This seminar will help you understand in detail the application of FDA’s 21 CFR Part 11 guidance on electronic records/electronic signatures (ER/ES) for computer systems subject to FDA regulations
MP3 Download This webinar will cover the key aspects of complying with 21 CFR Part 11 in both validating systems and maintaining them in a validated state throughout their entire life cycle.
MP3 Download This Webinar will explain what 21 CFR Part 11 is, why it is important to FDA-regulated companies, and how conformance to Part 11 differs from just having good IT security
MP3 Download The attendee will learn a simple way to address both data integrity and Part 11 aspects of the system, focusing on risk and critical thinking
Aug 06-07 This course benefits anyone that uses computer systems to perform their job functions and is ideal for professionals working in the health care, clinical trial, biopharmaceutical, and medical device sectors
MP3 Download describes exactly what is required for compliance with Part 11
MP3 Download Duration 180 Minutes
MP3 Download This course will provide an overview of requirements for aseptic and bulk manufacturing operations, including facility design and contamination
MP3 Download This webinar will review the regulatory requirements for investigating an OOS Investigation.
MP3 Download This session will give you a good understanding of how the IEC 62304 differs from ISO 13485. It will also cover components of the Software
This webinar will focus on cybersecurity of medical devices
On Demand Webinar Duration 360 minutes
MP3 Download This webinar will cover FDA and NB expectations for Quality Systems , Best Practices and How culture can impact quality and compliance risk in 2021
MP3 Download Pharmacovigilance Auditing Inspection course will explain how to prepare for the audit
MP3 Download The course provides insight into the ways in which Pharma 4.0™ will serve as an enabler for next generation medicinal products and new business cases for established products
MP3 Download Duration 90 Minutes
MP3 Download Duration 60 Minutes
June 03-05 In this course, general guideline for the determination of the analytical
MP3 Download In this live training webinar we will discuss the world-wide regulatory requirements for Annual product Reviews (or Product Quality Reviews).
On Demand Webinar Duration 120 minutes
On Demand Webinar Duration 60 minutes
On Demand Webinar Duration 60 minutes
MP3 Download The objective of this live, interactive WCS training seminar is to explore the role of aseptic filling to assure that manufactured product
MP3 Download this course we will review how quality systems helps in defining requirements for cleanrooms
MP3 Download You’ll learn an approach to both 21 CFR Part 11 and data integrity compliance understanding what FDA expects stakeholders in industry to do. There a few simple suggestions that can streamline validation activities related to all of these key areas.
Aug 26-28 This eight-hour vendor qualification audit training will help you improve
MP3 Download FDA Warning Letters and recent high-profile recalls indicate major cGMP deficiencies in many companies.
MP3 Download This course will provide participants with an understanding of how to effectively handle out-of-specification
MP3 Download Duration 90 Minutes
MP3 Download Duration 90 Minutes
MP3 Download -Duration 180 Minutes
MP3 Download This training will provide valuable assistance in process development include in Equipment Validation, Tracking, Calibration, and Preventive
May 19-20 this course will have understanding of concepts and statistical methods required in pharmaceutical, biological and medical device.
MP3 Download The session discussed GMP regulations, agency expectations, training program responsibilities, new employee requirements, transferred employees, external service providers, events, skills qualification program, assessment, retraining, instructor qualifications, curriculum, documentation, and performance deviations.
MP3 Download In this webinar speaker will define compliance, provide a translation of regulations and guidance into user requirements .
MP3 Download Defined Failure Investigation and Root Cause Analysis is a major tool in product complaint, non-conformance, and OOS failure investigations
MP3 Download Duration 90 Minutes
MP3 Download Duration 2 Day
MP3 Download Best QSR and ISO 13485 requirements webinar for management controls, Organizational structure and Establishment of an internal audit program.
MP3 Download In this course, you will learn the practical applications for ensuring regulatory compliance as required by FDA regulations
MP3 Download 3 day CSV course will teach you how to comply with key FDA and international CSV
MP3 Download Duration 90 Minutes
MP3 Download This webinar will include a comparison of the Agile and Waterfall methodologies, along with the pros and cons of each
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MP3 Download This Course will explain how to comply with key FDA and international CSV regulations
Jan 30 In this 90-minute accredited training, you will learn the importance of having a good
On Demand Webinar Duration 60 minutes
MP3 Download This webinar is based on information from the public domain, personal interviews, internet and social media discussions, news articles, and similar resources