Past Events (3,027)

Lead Auditor EN ISO 13485:2016 and EU MDR 2017/745 - Regulation

May 5, 2022 from 10am to 1pm – online Attend this webinar to understand, what are the changes to the previous medical device regulation and how to implement the changes in your current quality management system in a simple and quick way.… Organized by Complianceonline | Type: webinar

How FDA trains its investigators to review CAPA and what should you do to prepare

May 4, 2022 from 10am to 1pm – online This CAPA investigation training will discuss techniques used by the FDA to review your CAPA system. You will learn what the FDA tells their inspectors to focus in the QSIT document and how your comp… Organized by Complianceonline | Type: seminae

REACH and RoHS Compliance: Protecting Revenues with Advanced Compliance

April 28, 2022 at 7am to April 29, 2022 at 1pm – online This 2 day Virtual Seminar will go into the specifics of the REACH and RoHS regulations, provide case studies and share lessons learned so your organization can benefit from the mistakes of others. W… Organized by Complianceonline | Type: seminae

Lead Auditor EN ISO 13485:2016 and EU MDR 2017/745 - Regulation

April 21, 2022 at 9am to April 22, 2022 at 5pm – online The new medical device regulation EU MDR 745/2017 in the European Union has a lot of new requirements. This new regulation is also stronger connected to the EN ISO 13485:2016. The understanding of th… Organized by ComplianceOnline | Type: seminae

The 6 Most Common Problems in FDA Software Validation and Verification

April 20, 2022 from 10am to 1pm – online 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. Why Should You At… Organized by ComplianceOnline | Type: webinar
Clinical Data Management (CDM)

April 20, 2022 at 10am to April 21, 2022 at 4pm – online Clinical data management (CDM) is paramount for a successful research. After all, Garbage In, Garbage Out (GIGO). CDM involves all aspects of collecting, processing, and interpreting information. The… Organized by Complianceonline | Type: webinar

Risk-Based Approach to CSV, 21 CFR Part 11 and FDA Compliance

April 19, 2022 from 10am to 1pm – online FDA’s recent focus on data integrity during computer system validation inspections and audits has brought this issue to the forefront of importance for compliance of systems used in regulated industr… Organized by Complianceonline | Type: webinar

SOP Writing, Training and Compliance in the Pharmaceutical Industry

April 18, 2022 at 10am to April 19, 2022 at 5pm – online Standard Operating Procedures (SOPs) are the basis for a large part of the day-to-day training that most pharmaceutical employees are required to perform. Still, it is not widely understood the exten… Organized by ComplianceOnline | Type: seminae

Process Validation Guidance Requirements

March 31, 2022 at 10am to April 1, 2022 at 4pm – online The Process Validation Guidelines (January 2011) and the EU Annex 15: Qualification and Validation (October 2015) outline the general principles and approaches the two regulatory bodies consider appr… Organized by ComplianceOnline | Type: seminae

Project Management for FDA-Regulated Companies

March 30, 2022 from 10am to 1pm – online This project management training for FDA regulated companies will show how you can meet key FDA and EU MDD regulatory requirements for the project you manage. It will focus on proven tools and techni… Organized by Complianceonline | Type: webinar