PHT Corporation will demonstrate its market-changing LogPad App system for collecting secure patient-driven eData on the latest smartphones at the SCOPE Summit in Miami next month. PHT is the leading provider of technologies used to collectpatient-driven eData for clinical research.

This training on FDA supplier controls will help you refine your supplier chain management and vendor audits to match the FDA's tougher position. We will evaluate the chief areas of change to see how to better prepare a supplier chain management and audit program.

This Latin America regulatory compliance requirements training will cover topics relating to pre-clinical and clinical requirements, as well as, addressing the structure of the regulatory agencies in Latin America.

CSols, Inc. the premier Laboratory Informatics Consultancy in North America understands the complex challenges that today’s modern Laboratories face. As a result, CSols has developed five short courses to be presented at PITTCON 2014 on some of these critical business issues. These Short Courses provide both the training and tools that Laboratory and IT personnel can leverage to solve these business issues in their respective labs.

This medical device webinar will discuss strategies for meeting the Post Market Surveillance requirements as described in Annex X of the MDD (MDD 93/42/EEC, updated per the 2007/47/EEC M5 amendment, Annex 1: Essential Requirements), MEDDEV 2.7.1, Dec 2009 and ISO 14155.

FRISCO, Texas--(BUSINESS WIRE)--Web-based dairy supply chain solutions and market intelligence leader Dairy.com today announced the acquisition of QA Studio, a quality assurance and food traceability software provider to the dairy industry.

This FDA compliance webinar will help the attendees develop an effective training program and training plans for an organization. Attendees will learn GxP training requirements in US and EU.

This training on source water protection will focus on current microbiological indicators for assessing potability of water. Attendees will learn the best practices for the protection of source water and risk management from a microbiological perspective.

This webinar will provide an in-depth understanding of anti-kick back and stark laws, and discuss how marketing activities can trigger either or both. It will show how to implement mandatory internal controls to reduce exposure to risks.

This training on clinical compliance will focus on the requirements of trial master file (TMF) for pharmaceutical product, biotech, a medical device or a diagnostic product. Attendees will learn the best practices to ensure that the TMF is ready for inspection by the regulatory authority.

This training on FDA compliance will provide the attendees with an understanding of FDA expectations regarding end-of-phase 2A meeting guidance. Attendees will learn the best practices to comply with the intent of the guidance and to achieve a higher quality outcome from the meeting.

This two-day comprehensive Course on Latin America Regulatory compliance requirements will cover topics ranging from pre-clinical and clinical requirements through product registration, amendments and renewals across Pharmaceuticals, Biologics, Medical Devices and Combination Products. The Course will address the structure of the regulatory agencies in Latin America and discuss local cultural nuances to help you be successful in working with the regulators.

CompuGroup Medical US announced today that CGM LabDAQ LIS has been certified as a Gold Quality Solution by Quest Diagnostics under Quest's Health IT Quality Solutions™ Program (the "Program"). Quest Diagnostics is the world's leading provider of diagnostic information services.

This training on food safety compliance will provide the attendees with the knowledge of how food borne pathogens enter a food plant, expand its presence within the facility and contaminate the products. Attendees will learn the best practices for minimizing the presence of these pathogens in the food plant.

Learn how to use excel spreadsheet for GXP data to ensure compliance with 21 CFR Part 11 and reduce validation cost and time.

In this OSHA webinar, you will learn the rights and responsibilities for employers under the OSHA Act. For your full-time and temporary workers, you will be provided with the tools to stay compliant with the regulations and avoid penalties.

Thermo Fisher Scientific Inc., the world leader in serving science, is showcasing its online automation system configuration tool, the Thermo Scientific iAutomate™ at the Society for Laboratory Automation and Screening (SLAS), January 18-22. As a self-serve, free-to-use tool, iAutomate is designed to reduce the time associated with configuring and trialing an automation set-up.

LIMSABC, a leader in the Laboratory Information Management Systems industry has again, set a new standard for the LIMS software community. While working hand in hand with several medical and recreational marijuana facilities, LIMSABC has gone to great lengths to develop a cloud LIMS system to meet the requirements needed for these very specific labs and their needs.

The Journal of Biomolecular Screening (JBS) and the Journal of Laboratory Automation (JALA), both published by the Society of Laboratory Automation and Screening (SLAS) in partnership with SAGE Publications, hosted a special reception to celebrate the 2014 SLAS Journal Achievement Award honorees on Jan. 20 at SLAS2014, the Third Annual SLAS Annual Conference and Exhibition, Jan.18-22, 2014, in San Diego, Calif.

Sapio Sciences is pleased to announce the release of Exemplar NGS LIMS™. Sapio’s NGS LIMS system will track multiple next-generation sequencing (NGS) platform workflows from request through processing and analysis.