Past Events (3,027)

FDA Warning Letter Closeout Program

December 17, 2013 from 10am to 11am – Online Event This FDA warning letter closeout program will discuss how to successfully complete warning letter close out program which will help firm to obtain a closeout letter from FDA. Why Should You Attend: F… Organized by ComplianceOnline | Type: food, healthcare

Why and How - Verification of Compendial Methods - USP <1226>

December 12, 2013 from 10am to 11:30am – Online Event This USP <1226> webinar training will discuss the requirements of USP <1226>, what are FDA expectations related to method verification. Why Should You Attend: Analytics continues to be a… Organized by ComplianceOnline | Type: pharmaceutical
Mastering the HIPAA Privacy, Security, and Breach Notification Rules: Coping with Rule Changes, Managing Incidents, Preparing for Audits, and Avoiding Penalties: 2-day In-person Seminar

December 12, 2013 at 9am to December 13, 2013 at 6pm – Courtyard Miami Downtown Overview: 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 addressed for com… Organized by John Robinson | Type: conference
How to Prepare and Submit a Bullet Proof 510(k) and Latest FDA Proposed Changes to the Process: 2-day In-person Seminar

December 12, 2013 at 9am to December 13, 2013 at 6pm – DoubleTree by Hilton Hotel San Francisco Airport Overview: This Two-day course is a primer and overview to the premarket notification process, i.e., a 510(k). A 510(k) is a premarket submission made to FDA to demonstrate that your device to be mark… Organized by John Robinson | Type: conference

Audit Response: How to Protect Your Revenue through Timely and Accurate Responses

December 6, 2013 from 10am to 10:30am – Online Event This healthcare audit training will discuss the different deadlines and time frames for each auditing agency, the format for submission of information for each entity, the style and information neede… Organized by ComplianceOnline | Type: healthcare

Information on Cyber Security to Include in Medical Device Submissions

December 5, 2013 from 10am to 11:15am – Online Event This training will focus on the new draft guidance document recently released by the FDA on ensuring medical device cybersecurity. Attendees will gain insight into the security activities and documen… Organized by ComplianceOnline | Type: medical, related
Creating Effective SOP for Regulatory Compliance

December 5, 2013 from 10am to 11:30am – Online Event This FDA documentation webinar will explain the regulatory expectations for, and the proper design and maintenance of effective and compliant Standard Operating Procedures (SOPs). Why Should You A… Organized by ComplianceOnline | Type: fda, compliance
FDA Warning Letter Closeout Program

December 5, 2013 from 10am to 11am – Online Event This FDA warning letter closeout program will discuss how to successfully complete warning letter close out program which will help firm to obtain a closeout letter from FDA. Why Should You Attend:… Organized by ComplianceOnline | Type: fda, compliance
Validation and Use of Excel® Spreadsheets in Regulated Environments

December 5, 2013 from 10am to 10:30am – Online Event This excel validation training/ webinar will demonstrate how to design spreadsheets for part 11/GxP /SOX/HIPAA, document planning, specifications, installation, testing and changes to meet FDA requir… Organized by ComplianceOnline | Type: fda, validation

CLIA (Clinical Laboratory Improvement Amendments) Guidelines on Quality Control and Quality Assessment

December 4, 2013 from 10am to 11:15am – Online Event This Clinical Laboratory Improvement Amendments (CLIA) training will be valuable to CLIA regulated, non-waived laboratories that run automated analyzers or semi-quantitative kit tests. It will highli… Organized by ComplianceOnline | Type: clinical