Past Events (3,027)

November 8Monday

Recordkeeping and Documentation in a GLP Laboratory (US FDA, US EPA and OSHA Focus)

November 8, 2021 at 9:30am to November 9, 2021 at 5:30pm – online GLP requires many types of documents. The seminar covers both the general issues and many specifics that laboratories can receive a non-compliance on. These range from data recording to validation is… Organized by Complianceonline | Type: seminae
Case Management Boot Camp: Strategies for Success in the Acute Care Setting and Beyond!

November 8, 2021 from 9:30am to 5:30pm – online Please join us for this intense one-day program that will give you the skills to succeed as a case manager or social worker in the new era of value-based reimbursement and accountable care. The world… Organized by Complianceonline | Type: seminae
Case Management Boot Camp: Strategies for Success in the Acute Care Setting and Beyond!

November 8, 2021 from 8:30am to 5pm – online Please join us for this intense one-day program that will give you the skills to succeed as a case manager or social worker in the new era of value-based reimbursement and accountable care. The world… Organized by ComplianceOnline | Type: seminae
Accounts Payable Best Practices

November 8, 2021 at 8am to November 9, 2021 at 3pm – online Given the current business environment, mounting regulatory pressures, and the increased visibility and importance of the accounts payable function, best practices are something with which every prof… Organized by Complianceonline | Type: seminae

November 5Friday

The Use of Drug Master Files & Quality Agreements

November 5, 2021 from 11am to 5pm – online This combined DMF (Drug Master Files) and Quality Agreement training will discuss the advantages for suppliers and drug product manufacturers in developing these arrangements together. Over time, the… Organized by ComplianceOnline | Type: seminae
The Use of Drug Master Files & Quality Agreements

November 5, 2021 from 11am to 5pm – online This combined DMF (Drug Master Files) and Quality Agreement training will discuss the advantages for suppliers and drug product manufacturers in developing these arrangements together. Over time, the… Organized by Complianceonline | Type: seminae

November 4Thursday

GMP Environmental Monitoring for Pharmaceutical Clean Rooms

November 4, 2021 from 6pm to 7pm – online This webinar will discuss various US and international regulatory requirements, testing requirements for environmental monitoring program, current air and surface monitoring for measurement of no-via… Organized by ComplianceOnline | Type: webinar
Raw Material Requirements (Health Canada/USP/EP) in a cGMP Environment - Issues and Solutions

November 4, 2021 at 10am to November 5, 2021 at 4pm – online Raw material requirements in a cGMP environment are often overlooked as a Company develops new products. Depending upon the product being developed, e.g., tablets and capsules vs. biotechnology produ… Organized by ComplianceOnline | Type: seminae
Raw Material Requirements (Health Canada/USP/EP) in a cGMP Environment - Issues and Solutions

November 4, 2021 at 10am to November 5, 2021 at 4pm – online Raw material requirements in a cGMP environment are often overlooked as a Company develops new products. Depending upon the product being developed, e.g., tablets and capsules vs. biotechnology produ… Organized by Complianceonline | Type: seminae

October 25Monday

SOP Writing, Training and Compliance in the Pharmaceutical Industry

October 25, 2021 at 9pm to October 26, 2021 at 4:30pm – 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