Webinar On Ebola Outbreak: Guidelines and Startegies to Protect the Workplace by Vanessa Nelson at Compliance TrainingsScheduled On Monday, February 2, 2015 at 13:00 Hrs.Attend this webinar to learn about the Ebola virus, how is it transmitted, symptoms to look out for, how to prevent Ebola in the workplace, and the guidelines that should be followed to protect the workplace from this deadly threat.For more information visitcompliancetrainings.com/SiteEngine/ProductDetailView.aspx?id=HR1205

Webinar On Annual Reports for Approved PMAsScheduled On Thursday, December 11, 2014 at 13:00 HrsThis webinar describes the information required by FDA to be submitted in a PMA annual report. The webinar also discusses FDA recommendations for level of detail the applicant should provide in the PMA annual report.For more information visitcompliancetrainings.com/SiteEngine/ProductDetailView.aspx?id=FDB1402

Webinar On FDA Inspections : Managing the Myth and the RealityScheduled On : Wednesday, January 28, 2015 at 13:00 Hrs.This webinar will review principles of sterilization validation and using them as a benchmark for more robust cleaning validationOn Going Christmas Offers: Offer valid till 1 st January 2015.Register an attendee for Single Live:Get 10% of on every RegistrationFirst 10 attendees will receive recording Access to the webinar for No Additional CostFor Coupon Code call customer support: 416-915-4458For more information visitcompliancetrainings.com/SiteEngine/ProductDetailView.aspx?id=FDB1361

Webinar On FDA’s New Guidance On Medical Device Development Tools (MDDT) by Compliance TrainingsScheduled On Thursday, October 9, 2014 at 13:00 HrsSpeaker: Albert A. Ghignone, MS, RAC is the CEO of AAG Incorporated This webinar will discuss a voluntary process for qualification of Medical Device Development Tools (MDDT) for use in device development. An MDDT is a scientifically validated tool (test) to determine clinical outcome. For more information visitcompliancetrainings.com/SiteEngine/ProductDetailView.aspx?id=MD1401For immediate assistance contact us on 416-915-4458

Webinar On Best Practices for 510(k) Drafting and Submission: Dos and Don'tsScheduled On Friday, October 17, 2014 at 13:00 HrsSpeaker: Dr. David Lim President and Principal of Regulatory Doctor by Compliance Trainings.This session is a must for regulatory professionals working in medical device industry including those who are interested in the topic.For more information visitcompliancetrainings.com/SiteEngine/ProductDetailView.aspx?id=MD1354For immediate assistance contact us on 416-915-4458

Webinar on Medical Devices Designing with Cleanliness in MindScheduled On Monday, October 20, 2014 at 13:00 Hrs presenting by Kierstan Andrascik.This 60 minutes webinar will provide in-depth and valuable guidance to medical device manufacturers on design considerations for both single-use and re-usable devicesfor more information visitcompliancetrainings.com/SiteEngine/ProductDetailView.aspx?id=MD1144For  immediate assistance contact us on 416-915-4458

Webinar On 21 CFR 11 Compliance for Excel Spreadsheets Scheduled On Tuesday, October 21, 2014 at 13:00 Hrspresenting by Angela Bazigos.Spreadsheet Applications such as MS Excel are frequently used in 21 CFR 11 compliant environments, but they were not specifically designed for regulated environments and their development is not optimized for 21 CFR 11 complianceFor more information visitcompliancetrainings.com/SiteEngine/ProductDetailView.aspx?id=FDB1392For immediate assistance contact us on 416-915-4458

Webinar On Master Validation Planning To Meet U.S. FDA cGMP, ISO 13485, and ICH Q9 / ISO 14971 RequirementsThis 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 insufficient, poor or non-existent V&V planning.For more information visitcompliancetrainings.com/SiteEngine/ProductDetailView.aspx?id=MD1266For immediate assistance contact us on 416-915-4458

Webinar on Major Considerations for Expanding your Quality System requirements (QSR) from Medical Devices to Combination DevicesThis webinar presents important facts to simplify the planning and execution phase in your journey towards becoming a combination device manufacturer by incorporating the essential quality system requirements in your company.For more information visitcompliancetrainings.com/SiteEngine/ProductDetailView.aspx?id=MD1092For immediate assistance contact us on 416-915-4458

Webinar On The 510(k) Program: Substantial Equivalence In Premarket NotificationsThis webinar is a must for those personnel that require an understanding of the FDA's 510(k) substantial equivalence determinations.For more information visitcompliancetrainings.com/SiteEngine/ProductDetailView.aspx?id=MD1229

Webinar On FDA Regulation of Mobile Apps Scheduled On Monday, September 22, 2014 at 13:00 Hrs.The use of mobile apps as a medical device continues to mushroom. Approximately 85% of adults use cell phones. They offer a fertile field for mobile apps used for medical purposes, some good, some not. How do you decide which healthcare app is safe? Can someone hack an app you rely on for life supporting / life sustaining medical care? Yes. For more information visitcompliancetrainings.com/SiteEngine/ProductDetailView.aspx?id=FDB1127

Webinar On Statistical Analysis of GagesScheduled On Friday, September 25, 2014 at 13:00 HrsThe seminar begins with an examination of the fundamental vocabulary and concepts related to metrology. Topics include: accuracy, precision, calibration, and "uncertainty ratios". For more information visitcompliancetrainings.com/SiteEngine/ProductDetailView.aspx?id=FDB1272

Webinar On Meeting Magic: Facilitation & Planning Skills for Meeting Productivity Scheduled On Tuesday, September 9, 2014 at 13:00 Hrs.This webinar will help to develop the skills to plan, facilitate, and evaluate meetings; to decrease the number and length of meetings while gaining more active participation from meeting attendees.For more information visitcompliancetrainings.com/SiteEngine/ProductDetailView.aspx?id=HR1175

Webinar On Current GMP Requirements for Combination Products - Final Rule Scheduled On : Thursday, September 4, 2014 at 13:00 HrsThis webinar discusses this final rule and describes approaches to comply.At the end of this session, you will be ableTo understand where the combination products GMP rule applies.For more information visitcompliancetrainings.com/SiteEngine/ProductDetailView.aspx?id=FDB1062