All John Robinson webinar Events (46)

6-Hour Virtual Seminar on Master Class for the HIPAA Officer: Protecting Patient Information and Implementing Today's Privacy, Security, and Breach Regulations

March 10, 2020 from 8am to 2pm – Online Event The session begins with overview of the HIPAA regulations and then continues with presentation of the specifics of the Privacy Rule, such as Individual Rights and Uses & Disclosures, and recent a… Organized by John Robinson | Type: webinar

6-Hour Virtual Seminar on Auditing Analytical Laboratories for FDA Compliance

March 5, 2020 from 8am to 2pm – Online Event There are two phases to this topic. The first is auditing itself. Good audits are well structured. They must consider the reasons for the audit, the regulatory requirements, as well as the nature of… Organized by John Robinson | Type: webinar

Explore New SAMHSA Confidentiality Law for Substance Use Disorder Records(42 CFR Part 2)

March 3, 2020 from 10am to 11am – Online Event Overview: This lesson will be addressing how practice/business managers (or compliance offers) need to ensure their organization is complying with the Federal Substance Abuse and Mental Health Admini… Organized by John Robinson | Type: webinar

6-Hour Virtual Seminar on Tougher Import Rules for FDA Imports in 2020

March 2, 2020 from 8am to 2pm – Online Event Importing FDA regulated products requires careful planning before you even start. Registration, product compliance, record and data submission must be exactly correct or your product will be detained… Organized by John Robinson | Type: webinar

How FDA Trains its Investigators to Review CAPA and What You Should Do to Prepare

August 27, 2014 from 10am to 11am – Online Event Overview: During an inspection, FDA personnel will take a great deal of time reviewing your company's CAPA system. What will they look for? This session will discuss all the documents used by FDA to… Organized by GlobalCompliancePanel | Type: webinar, pharma, medical, clinical, health

Stability Program in Drug Development: A Comprehensive Approach

August 21, 2014 from 10am to 11am – Online Event Overview: The objective of this web seminar is to provide a comprehensive overview of the approach used to establish an effective and compliant stability program for small molecule pharmaceuticals. D… Organized by GlobalCompliancePanel | Type: webinar, pharma, medical, clinical, health

The Most Common Problems with Software Validation Processes

August 20, 2014 from 10am to 11:30am – Online Event Overview: This webinar covers the fundamentals of 21 CFR Part 11, software validation, and computer system validation. It provides details for company compliance including GAMP, qualification, and va… Organized by GlobalCompliancePanel | Type: webinar, pharma, medical, clinical, health

Measurement Uncertainty in Microbiology

August 18, 2014 from 10am to 11am – Online Event Overview: Many microbiology laboratories are confused about what MU is, how to calculate it and how to apply it. We will discuss what is needed to meet the accreditation requirement for MU, including… Organized by GlobalCompliancePanel | Type: webinar, pharma, medical, clinical, health

Quality Management Systems - Creating, Implementing and Improving

August 14, 2014 from 10am to 11am – Online Event Overview: Today's manufacturers face enormous challenges managing their quality and compliance initiatives. Market trends point to even greater scrutiny of these efforts as pressure mounts from both… Organized by GlobalCompliancePanel | Type: webinar, pharma, medical, clinical, health
Understanding Combination Products, Requests for Designation and Product Jurisdiction

August 14, 2014 from 10am to 11am – Online Event Overview: This webinar will provide a detailed discussion of understanding the definition of a combination product, the categories of combination products, how combination products are reviewed, how… Organized by GlobalCompliancePanel | Type: webinar, pharma, medical, clinical, health