Events tagged "online IT course":

Process Validation for Medical Device Manufacturers Webinar

Online Event

Process Validation for Medical Device Manufacturers Webinar logo

The US FDA has required medical device manufacturers to validate certain production processes since the 1980′s. Recently the Center for Devices and Radiological Health (CDRH) recognized the Global Harmonization Task Force (GHTF) guidance on Process Validation. Read more »

Navigating the new FDA world of Combination Products – Webinar By ComplianceOnline

Online Event

Navigating the new FDA world of Combination Products   Webinar By ComplianceOnline logo

Why Should You Attend: It’s no longer just the “drug-eluting stent” that the FDA sees as a combination product, but also the drug being delivered in a pre-loaded syringe, or by a programmable pump. Drug-device interactions need to be specifically tested and the specific compatibility/stability test result information listed in the label. Read more »

HIPAA Business Associates: How the regulations have changed, and what you need to do for compliance now – Webinar By GlobalCompliancePanel

Online Training Webinar

HIPAA Business Associate rules have changed in fundamental ways, with new responsibilities and obligations for HIPAA BAs. Read more »

Understanding ISO 13485 vs. ISO 9001 for Successful QMS in Medical Device Industries – Webinar By GlobalCompliancePanel

Online Training Webinar

ISO 13485:2003 is a quality management system standard specially written for the medical device industry and is on the U S Food & Drug Administration (FDA) list of recognized consensus standards. Read more »

Data Security Analysis for Healthcare Providers – Webinar By GlobalCompliancePanel

Online Training Webinar

Data Security Analysis for Healthcare Providers: The “meaningful use” rules relating to the adoption of Electronic Medical Records require regular assessment of data security risks. HIPAA re-contains similar requirements. Read more »

Chemical Control for Food Manufacturers: Ingredient, Cleaning and Hazardous Materials – Webinar By GlobalCompliancePanel

Online Training Webinar

Overview: A comprehensive review of an ideal chemical control program will be presented.

The guidelines presented will enable your company to implement programs that are cost effective and meet or exceed the expectations of major QSR, and GFSI audit criteria. Read more »

Change Control – Your Company’s GMP Weak Point – Webinar By GlobalCompliancePanel

Online Training Webinar

Overview:  There is a pervasive public perception that the FDA has been ineffective in protecting the public.

Recent news events in foods, drugs, and devices seem to support this perception.  The “tougher” FDA is determined to change that perception. Industry must be prepared to adapt, and recognize that such adaptation will actually work to their long-term benefit. Read more »

The International Arab Conference on Information Technology (ACIT 2011) / Riyadh, Saudi Arabia

December 11, 2011toDecember 14, 2011

Naif Arab University for Security Science (NAUSS),
Riyadh, Saudi Arabia

The International Arab Conference on Information Technology (ACIT 2011) / Riyadh, Saudi Arabia logoThe International Arab Conference on Information Technology (ACIT’2011) is a forum for scientists, engineers, ‎and practitioners to present their latest research, results, ideas, developments, and applications in all areas of ‎information technology. Read more »

Webinar: Intro to Socrates – Developing Prescriptive Applications

Online Event

Webinar: Intro to Socrates   Developing Prescriptive Applications logoIn this free webinar, Clive Bearman, Active Endpoints Director of Product Marketing, introduces you to Socrates, an innovative solution for building simple, yet powerful, web applications that guide users to specified outcomes. Read more »

Social Media in a Regulated Environment – Webinar By ComplianceOnline

Online Event

Social Media in a Regulated Environment   Webinar By ComplianceOnline logoWhy Should You Attend:
Social Networking is considered by FINRA to be “communicating with the public”, and as such subject to rigorous rules, regulations, and procedures that if not followed can lead to fines and disciplinary action to both the Registered Representative (RR) and their parent Broker-Dealer firm. Read more »

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