Past Events (3,027)

February 17Thursday

FDA Compliance and Clinical Trial Computer System Validation

February 17, 2022 at 11am to February 18, 2022 at 5pm – online Course Description: The FDA governs the computer systems used to collect, analyze, transfer and report data that is in support of human clinical trials required for drug approval. FDA oversight is ba… Organized by ComplianceOnline | Type: seminae
Monitoring High Risk Transactions

February 17, 2022 from 10am to 1pm – online This BSA/AML (Bank Secrecy Act/ Anti Money Laundering) compliance training will help attendees understand, identify and mitigate the risks associated with high risk transactions. Why Should You Atten… Organized by ComplianceOnline | Type: webinar

February 16Wednesday

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

February 16, 2022 from 10am to 1pm – online Learn how to use Microsoft Excel spreadsheets for GXP data to ensure compliance with 21 CFR Part 11 and reduce validation cost and time. Organized by Complianceonline | Type: webinar
Building a Vendor Qualification Program for FDA Regulated Industries

February 16, 2022 at 10am to February 17, 2022 at 5pm – online This course will provide detailed explanations and examples for Building a Vendor Qualification Program for FDA Regulated Industry. With today’s pharmaceutical market, raw materials, Active Pharmaceu… Organized by ComplianceOnline | Type: seminae
CMS Two Midnight Rule

February 16, 2022 from 10am to 1pm – online Attend this webinar to learn the CMS new regulation "the two midnight rule" and what are the medical and financial outcomes of the rule and how to apply the rule correctly to remain CMS compliant and… Organized by ComplianceOnline | Type: webinar
Clinical Data Management (CDM)

February 16, 2022 at 10am to February 17, 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: seminae
Writing High-Impact Executive Summaries

February 16, 2022 from 9am to 12pm – online This training program will help attendees approach the writing situation with a clear and useful strategy. It will include strategies to fuse the purpose of the summary with the issues that matter to… Organized by ComplianceOnline | Type: webinar

February 15Tuesday

How to Create Clinical Evaluation According to EU MDR 2017/745 Article 61 and Annex XIV?

February 15, 2022 from 10am to 6pm – online The new medical device regulation EU MDR 745/2017 in the European Union has a lot of new requirements. One hot topic is the focus on the clinical data, “Clinical Evaluation-Process” and the new requi… Organized by ComplianceOnline | Type: seminae

February 14Monday

Medical Device Quality Systems, CAPA and European Medical Device regulations

February 14, 2022 at 8am to February 15, 2022 at 3pm – online Medical Device Companies must meet the regulatory requirements to “establish and maintain” a quality management system (QMS). This 2-day seminar will cover the essentials of compliance for medical de… Organized by ComplianceOnline | Type: seminae

February 11Friday

Navigating California Prop 65 Incorporating FSMA Preventative Controls, Best Practice Approach

February 11, 2022 from 10am to 1pm – online Attention Food Manufacturers, attend this webinar to learn latest FSMA based strategies to navigate the complexity under Prop 65. Prop 65 is an ever-changing regulatory arena, with complex requiremen… Organized by ComplianceOnline | Type: webinar