Upcoming conferences about Medical Supplies & Equipment

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.

By : Compliance online

World Vaccine Congress Asia 2012 is the largest Asian vaccine conference which brings together the entire value chain of the vaccine industry.

By : Terrapinn Pte Ltd

Please join Michelle Engler, the creator of Accel-Copy, for a one-hour presentation that will include a live demonstration of Accel-Copy.

By : BioPharm Systems

This interactive two-day course explores proven techniques for reducing costs associated with implementing, using, and maintaining computer systems in regulated environments. Attendees learn how to decrease software implementation times and lower costs using a 10-step risk-based approach.

By : Compliance online

This webinar on Trial Master File (TMF) for clinical research sites will show how you can create an FDA compliant TMF to ensure that it will pass inspection by FDA investigators and QA Auditors.

By : Compliance online

Leading provider of Oracle's clinical trial, data, and drug safety software will discuss a major pharmaceutical company's pharmacovigilance globalization initiative that helped standardize and streamline its operations.

By : BioPharm Systems

Interdisciplinary field of study that underlines the use of computer and communication technology to help assisting healthcare professionals in the process of diagnosis, treatment, monitoring, medication prescription, referral, information retrieval and communication, documentation and transactions.

By : INSTICC

This FDA Software Validation and Verification training/webinar will review the validation planning process with particular emphasis on avoiding six common pitfalls.

By : Compliance online

Keeping up to date with developments in the treatment of viral hepatitis is a major challenge to treating physicians, healthcare providers and researchers. The Viral Hepatitis Congress provides an accessible forum for objective scientific assessment of new drug treatments and therapeutic strategies.

By : KnowledgePoint360 Group

This conference showcases the latest medical and healthcare products, technologies, developments and services, and is supported by governmental and major local and regional organizations.

By : Al Atheen

his seminar includes an overview of the ISO 13485 standard to understand the requirements as well as practical methods to implement a successful quality management system.

By : Compliance online

This seminar will discuss the 510(k) and PMA submissions and will walk you through how to format a succinct and comprehensive 510(k) and premarket approval (PMA) application to increase submission quality and to proactively facilitate the review process in a streamlined manner.

By : Compliance online

How to mobilize healthcare content to engage and provide information to your stakeholders.

By : Health Network Communications

This 3-hr virtual seminar will provide an introduction to FDA’s Regulation of Medical Devices and is intended for the Beginner.

By : Compliance online

This 6-hr virtual seminar will present a detailed overview of regulatory requirements necessary for establishing a medical device quality system in the US, which is relevant and applicable for quality system management in global jurisdictions of medical device products.

By : Compliance online

This will provide valuable assistance and give a process and procedure to all regulated companies that are transferring equipment, molds, dies, systems and processes to suppliers. It will show how quality, verifications and validations process will meet today’s standards for the FDA and CE Mark.

By : Compliance online

In this seminar you will be provided a basic understanding of radiation and EO sterilization processes and validation methods associated with both methods.

By : Compliance online

This 90-minute webinar will help you understand the 510K process including some history about 510ks versus PMAs and give you the necessary information to know when to file a 510k, as opposed to a PMA, or to not file any 510K of a new or existing medical device.

By : Compliance online

It will discuss the requirements and compliance in medical device adverse event reporting and medical device surveillance/vigilance system in the US, Europe and Canada.

By : Compliance online

This 90-minute webinar on Advanced Methods of Root Causes Analysis, for medical device companies, will cover principles and methods of Root Cause Analysis (RCA) and review proven techniques for ISO 14971 Risk Reduction based on RCA.

By : Compliance online

This sterilization validation process training webinar will review the FDA or ISO requirements for tests following validation and emphasis is placed on the appropriate tests for validation, the appropriate routine tests and the frequency of testing.

By : Compliance online

“Uniting industry leaders to analyse advanced commercial developments & to identify successful management strategies of Biosimilars”

By : virtue Insight

This webinar will cover the basics of design controls for medical devices, and provide recommendations for implementation of a compliant design control system. Also discussed will be design control requirements for devices already in distribution.

By : Compliance online

Improving Efficiency by Maintaining a Dynamic Internal Audit Strategy

By : marcus evans