Past Events (3,027)

Analytical Method Validation, Verification and Transfer

December 8, 2021 at 9am to December 9, 2021 at 4pm – online Reliable analytical results are necessary to make informed decision about the quality and safety of the products in the pharmaceutical industry. In addition, such analytical data are required for reg… Organized by ComplianceOnline | Type: webinar

Validation Master Plan - The Unwritten Requirements

December 7, 2021 from 10am to 1pm – online This 60-minute session on master verification and validation planning will discuss the major cGMP deficiencies and "must have" elements from the U.S. FDA cGMP, ICH Q9 and ISO 14971 for hazard analysi… Organized by ComplianceOnline | Type: webinar
How to Achieve a Compliant and Effective Cleanroom Design and Facility Validation

December 7, 2021 from 10am to 1pm – online This training program will discuss designing an effective cleanroom facility validation protocol and report, when and how to transition into the routine environmental monitoring processes, how to mai… Organized by ComplianceOnline | Type: webinar
FDA's Ambitious Regulation of Social Media

December 7, 2021 from 10am to 1pm – online FDA regulates advertising and promotion material as labeling. The legal definition of labeling covers just about anything that explicitly or implicitly conveys a message intended to affect a person’s… Organized by Complianceonline | Type: webinar
How To Build a Profitable Generic Pipeline Before Your Competition

December 7, 2021 from 6am to 9pm – online We all want to have a great generic portfolio, but all our competitors also want the same thing - so how do you make sure that you get the winners to market before they do? Do you go for supergeneric… Organized by Complianceonline | Type: webinar

An Update on Discharge Planning Rules and Regulations for 2022

December 6, 2021 from 10am to 1pm – online In this program we will start by reviewing the current rules for discharge planning. Are you compliant with these rules? The newly enacted rules that are now required under the Medicare program’s con… Organized by Complianceonline | Type: webinar
Non-conforming Materials and Failure Investigations for Medical Devices

December 6, 2021 from 10am to 1pm – online Non-conforming material happens. And medical device companies must deal it. This 90-minute webinar will help you to make sense of confusing regulations and effectively deal with non-conforming materi… Organized by ComplianceOnline | Type: webinar
Strategies To Prevent Manufacture And Distribution Of Substandard Medications

December 6, 2021 from 10am to 1pm – online Substandard medications, like counterfeit drugs, present a real and increasing danger both to patients and companies. In this webinar, learn how to take a proactive approach to stay ahead of these pr… Organized by ComplianceOnline | Type: webinar

Medical Device Single Audit Program [MDSAP] Implementation

December 2, 2021 from 11am to 5pm – online Global Medical Device Regulations continue to evolve, as devices become more diverse and sophisticated. Understanding the regulations and requirements in your targeted markets will expedite speed-to-… Organized by ComplianceOnline | Type: seminae
Process Validation Guidance Requirements (FDA and EU Annex 15: Qualifications and Validation)

December 2, 2021 at 10am to December 3, 2021 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