Past Events (3,027)

November 14Friday

Webinar On Corrective and Preventative Action (CAPA) Throughout the Product Lifecycle

November 14, 2014 from 1pm to 2:30pm – Online This webinar will discuss how the CAPA system and associated processes such as design control, risk management, process control, and investigations can be utilized throughout the product lifecycle to… Organized by Compliance Trainings | Type: webinar

November 13Thursday

Webinar On Confidence / Reliability Calculations & Statistically Valid Sample Sizes

November 13, 2014 from 1pm to 2:30pm – Online All manufacturing and development companies perform testing and/or inspections that involve concluding whether or not a product or lot is acceptable vs. design or QC specifications. Such test/inspect… Organized by Compliance Trainings | Type: webinar

November 6Thursday

Webinar on Best Practices for Medical Device Recalls

November 6, 2014 from 1pm to 2pm – Online In the United States, medical device firms are subject to compliance to the FDA regulations of device recalls, correction and removals. To achieve compliance and to remain compliant, it is critical t… Organized by compliancetrainings | Type: webinar

October 30Thursday

2-day In-person Seminar on “Quality Audits for the Medical Device Industry” at Raleigh, NC

October 30, 2014 at 9am to October 31, 2014 at 6pm – Raleigh, NC Summary of the workshop: Quality audits are an important element in checking the health of a Quality Management System (QMS). Audits are one of the most powerful tools that management has to assure o… Organized by GlobalCompliancePanel | Type: seminar, pharma, medical, clinical, health, compliance, regulatory, fda
2-day In-person Seminar on “Combination Products: How to Get Your Combination Product Approved and onto the US Marketplace” at San Francisco

October 30, 2014 at 9am to October 31, 2014 at 6pm – San Francisco, CA, USA Summary of the workshop: This course provides a comprehensive understanding of the FDA Combination Product system. Participants receive a foundation of knowledge about the FDA Office of Combination P… Organized by GlobalCompliancePanel | Type: seminar, pharma, medical, clinical, health, compliance, regulatory, fda
2-day In-person Seminar on “The A to Z's of HIPAA Privacy, Security, and Breach Notification Rules” at Raleigh, NC

October 30, 2014 at 9am to October 31, 2014 at 6pm – Raleigh, NC Summary of the workshop: This session is designed to provide intensive, two-day training in HIPAA compliance, including what's new in the regulations, what's changed recently, and what needs to be ad… Organized by GlobalCompliancePanel | Type: seminar, pharma, medical, clinical, health, compliance, regulatory, fda

October 24Friday

Webinar on Major Considerations for Expanding your Quality System requirements (QSR) from Medical Devices to Combination Devices

October 24, 2014 from 1pm to 2pm – Online Differences in regulatory requirements between Medical Devices and Pharmaceutical products poses unique challenges to companies that want to manufacture devices that contain drugs and biological prod… Organized by compliancetrainings | Type: webinar

October 23Thursday

2-day In-person Seminar on “Applying ISO14971:2012 and IEC62304 - A Guide to Practical Risk Management” in Berlin, Germany

October 23, 2014 at 9am to October 24, 2014 at 6pm – Berlin, Germany Summary of the Workshop: Gaps, incorrect or incomplete implementation of safety functionality can delay or make the certification/approval of medical products impossible. Most activities cannot be re… Organized by GlobalCompliancePanel | Type: seminar, pharma, medical, clinical, health, compliance, regulatory, fda
2-day In-person Seminar on “Quality System Regulations for Drugs, Devices, and Tablets and How to generate your DMF” at Philadelphia

October 23, 2014 at 9am to October 24, 2014 at 6pm – Philadelphia, PA Detailed Description: Primary Student Objectives - General High Level Topics where we will move down to very specific discussion and details to generate a much higher comprehension for quality indivi… Organized by GlobalCompliancePanel | Type: seminar, pharma, medical, clinical, health, compliance, regulatory, fda

October 22Wednesday

Webinar On Master Validation Planning To Meet U.S. FDA cGMP, ISO 13485, and ICH Q9 / ISO 14971 Requirements

October 22, 2014 from 1pm to 2:30pm – Online This 90 minute in-depth webinar discusses the FDA Warning Letters and recent high-profile recalls indicate major cGMP deficiencies in big name device and pharma companies, many going back to insuffic… Organized by compliancetrainings | Type: webinar