Past Events (3,027)

Webinar on Extending Your Quality System from Medical Devices to Manufacturing of Combination Products, Your Unique Challenges and How to Overcome them

May 15, 2015 from 2pm to 2pm – Canada Description : This webinar presents important facts to simplify the planning and execution phase in your journey towards becoming a combination device manufacturer by incorporating the essential qua… Organized by Compliance Trainings | Type: webinar

Webinar On HIPAA – How to Put a Compliance Program in Place

May 12, 2015 from 1pm to 2pm – Online Description : Being in compliance with HIPAA involves not only ensuring you provide the appropriate patient rights and controls on your uses and disclosures of protected health information, but you a… Organized by Compliance Trainings | Type: webinar
Webinar On Sampling: How Large a Sample Do I Need? Determining the Right Size for Accurate, Cost Effective Results

May 12, 2015 from 1pm to 2pm – Canada Description : This webinar provides some practical and useful answers to this question. Methods for determining appropriate sample sizes in raw materials acceptance, finished product release, proces… Organized by Compliance Trainings | Type: webinar
Webinar On Managing the FDA form "483": Inspection Observations

May 12, 2015 from 1pm to 2pm – Canada Description : This webinar is a complete guide on how to manage the FDA's 483 observations during and after an inspection. How you respond can make or break you. Form FDA 483 is a list of observation… Organized by Compliance Trainings | Type: webinar
Webinar On Managing the FDA form "483": Inspection Observations

May 12, 2015 from 1pm to 2pm – Online This webinar is a complete guide on how to manage the FDA's 483 observations during and after an inspection. How you respond can make or break you. Areas Covered in the Session : What the Form FDA “4… Organized by complianceTrainings | Type: webinar

Webinar On Learning from Recent FDA Warning Letters related to Part 11 and Computer Validation

May 7, 2015 from 1pm to 2:15pm – Canada Description : Some time ago FDA started the Part 11 inspection initiative. While originally the initiative was supposed to last 3-6 months, now it looks more like an ongoing program with Part 11 rela… Organized by Compliance Trainings | Type: webinar
FDA Inspections: Before, During and After - 2-day In-person Seminar

May 7, 2015 at 9am to May 8, 2015 at 5pm – Four Points By Sheraton French Quarter Overview: FDA's inspection program follows well-established procedures and conducts the inspections with as much consistency as possible. FDA trains its investigators from day one. During the first s… Organized by GlobalCompliancePanel | Type: food, fda, medical, device, defence, and, navy, aerospace, mining
The Statistics of: Design Verification, Process Validation, and Statistical Process Control

May 7, 2015 at 9am to May 8, 2015 at 6pm – Raleigh, NC Overview: This 2-day seminar provides a 1-day introduction to the statistical tools used to analyze Design Verification data and Process Validation results. The 2nd day is spent on Statistical Proces… Organized by GlobalCompliancePanel | Type: food, fda, medical, device, defence, and, navy, aerospace, mining

Webinar On Verification vs Validation

May 6, 2015 from 1pm to 2pm – Canada Description : This webinar will focus on the difference between Verification vs Validation and how can we use them to improve the bottom line. If Verification &Validation are done right, the proc… Organized by Compliance Trainings | Type: webinar

Webinar On 21 CFR 11 Compliance for Excel Spreadsheets

May 5, 2015 from 1pm to 2pm – Canada Description : In Dec. 2010, the FDA has stepped up enforcement for 21 CFR 11 compliance with spreadsheets being considered as low hanging fruit for FDA inspectional findings. Spreadsheet Applications… Organized by Compliance Trainings | Type: webinar