Past Events (3,027)

Customer Interactions: Law, Policies, Ethics

August 6, 2014 from 10am to 11:30am – Online Event Overview: The proliferation of legal requirements (law and regulation) governing the financial relationships between medical product companies and the doctors who order their products has led to what… Organized by GlobalCompliancePanel | Type: webinar, pharma, medical, clinical, health

Webinar On Statistical Analysis of Gages

August 5, 2014 from 1pm to 2pm – Online The seminar begins with an examination of the fundamental vocabulary and concepts related to metrology. Topics include: accuracy, precision, calibration, and "uncertainty ratios". Several of the stan… Organized by compliancetrainings | Type: webinar
Webinar on Current Good Manufacturing Practices (cGMP) for Medical Devices and IVDs

August 5, 2014 from 1pm to 2pm – Online The US Food and Drug Administration (FDA) states in warning letters “this inspection revealed that these devices are adulterated within the meaning of section 510(h) of the FD&C Act, in that the… Organized by compliancetrainings | Type: webinar
Key Concepts in Successful Water System Sanitization

August 5, 2014 from 10am to 11:30am – Online Event Overview: Though hardly a water system is designed and installed without some capability of sanitization, the system design features, materials of construction, sanitization chemical choices and how… Organized by GlobalCompliancePanel | Type: webinar, pharma, medical, clinical, health

Webinar on Proactive Internal Auditing-The Key to Establishing, Maintaining, and Improving Quality Systems

August 4, 2014 from 1pm to 3pm – Online This webinar provides a broad overview of the internal auditing functions starting with the concept of quality systems and their objectives, primarily using graphical methods. The webinar focuses on… Organized by compliancetrainings | Type: webinar

2-day In-person Seminar on Global Medical Device Regulation at Denver, CO

July 31, 2014 at 9am to August 1, 2014 at 6pm – WILL BE ANNOUNCED SOON Overview: This course provides an overview of international medical device regulations. Beginning with a discussion of the similarity of global requirements, including both voluntary and mandatory st… Organized by GlobalCompliancePanel | Type: seminar, pharma, medical, clinical, health, compliance, regulatory, fda

21 CFR Part 820 - Quality System Regulation - Applying Principles of Lean Documents and Lean Configuration

July 30, 2014 from 10am to 11am – Online Event Overview: All life science businesses are required to maintain their Quality Management System (QMS) processes in a state of control, via controlled documents and objective evidence in the form of re… Organized by GlobalCompliancePanel | Type: seminar, pharma, medical, clinical, health, compliance, regulatory, fda
Combination Products: FDA's Proposed Rule for GMP Requirements and Introduction and Expectations for "Combo" Products

July 30, 2014 from 10am to 11am – Online Event Overview: What is a combination product? What are some examples of combination products? How are combination products assigned for review? Where can I find guidance for how master files can be used i… Organized by GlobalCompliancePanel | Type: seminar, pharma, medical, clinical, health, compliance, regulatory, fda

Best Practices in Supplier Management

July 29, 2014 from 10am to 11am – Online Event Overview: Supplier qualification and assessment is required in both the QSR regulations and ISO standards.Many companies spend a great deal of time and money in pursuit of compliance with this. Many… Organized by GlobalCompliancePanel | Type: seminar, pharma, medical, clinical, health, compliance, regulatory, fda
FDA Device Software Regulation

July 29, 2014 from 10am to 11am – Online Event Overview: Software's level of complexity and use is expanding at exponential levels. Likewise the potential risks to health follow suit. Problems with software create a number of different hurdles. S… Organized by GlobalCompliancePanel | Type: seminar, pharma, medical, clinical, health, compliance, regulatory, fda