Past Events (3,027)

Webinar on Test Methods and Standards for Design Verification & Validation

July 29, 2016 from 1pm to 2pm – Online Description : Design Control is an integral part of any quality system in regulated industries. FDA Quality System regulation, Quality System Inspection Techniques (QSR and QSIT) and ISO 13485: 2016… Organized by Compliance Trainings | Type: webinar

Webinar on FDA Compliance and Laboratory Computer System Validation

July 27, 2016 from 1pm to 2pm – Online Description : You should attend this seminar if you are responsible for planning, executing or managing the validation of laboratory computer systems governed by FDA regulations. Effective and compli… Organized by Compliance Trainings | Type: webinar
Webinar on How to Detect Lack of Data Integrity

July 27, 2016 from 1pm to 2pm – Online Description : Data are central to the development, manufacture and marketing of pharmaceuticals of all types. The renewed interest in data integrity raises questions regarding what is data integrity… Organized by Compliance Trainings | Type: webinar
Ensuring a Successful Collaboration between Sponsors and CROs

July 27, 2016 from 10am to 11am – Online This session will focus on the keys to finding a good sponsor/CRO match for your clinical research. We will discuss ways to manage the work to ensure that the clinical study is completed as effective… Organized by Xtalks Life Science Webinars | Type: webinar

Webinar on Root Cause Analysis

July 26, 2016 from 1pm to 2pm – Online Description : Root cause analysis (RCA) involves searching backwards from an undesirable effect (or problem) to its cause(s) and addressing those causes. While the term "Root Cause" implies that ther… Organized by Compliance Trainings | Type: webinar

Webinar on FDA New Requirements for Pyrogen and Endotoxin Testing for Drugs, Biologics and Medical Devices

July 25, 2016 from 1pm to 2pm – Online Description : This presentation is intended to discuss current FDA requirements for pyrogen and endotoxins testing required for drugs, biologics and medical devices for regulatory purposes. In parti… Organized by Compliance Trainings | Type: webinar
Webinar on FDA Audit Practices and the 10 Most Common Cited GMP Deficiencies

July 25, 2016 from 1pm to 2pm – Online This webinar will look at changes in FDA’s approach to audits and the current method used to determine audit frequencies by using a system of risk assessments. Within the industries of pharma, biotec… Organized by Compliance Trainings | Type: webinar

Webinar on Writing Effective SOPs for Medical Device Quality Management Systems

July 22, 2016 from 1pm to 2pm – Online This webinar will help you to write clear, unambiguous, yet flexible SOPs. You will learn techniques for creating easy to read, clear, and concise SOPs that your employees can easily follow. Well wri… Organized by Compliance Trainings | Type: webinar

Webinar on Self – Disclosure to the OIG - When / Why and How to do it

July 21, 2016 from 1pm to 2pm – Online The course will allow your organizational to increase their knowledge base and facilitate their ability to determine if they need to disclose information to the OIG or not. It will also increase thei… Organized by Compliance Trainings | Type: webinar
Webinar on Transfer of Analytical Methods and Procedures according to USP 1224

July 21, 2016 from 1pm to 2pm – Online Description : When validated methods are transferred between laboratories and sites, their validated state should be maintained to ensure the same reliable results in the receiving laboratory. For a… Organized by Compliance Trainings | Type: webinar