3-hr Virtual Seminar: Preparing the OSHA 300A Annual Injury and Illness Summary-Understanding the OSHA Recordkeeping Requirements
This OSHA Recordkeeping training will address the key concepts in understanding the OSHA recordkeeping analysis through recent OSHA Interpretation Letters. This training will include hypothetical fact scenarios that present common recordkeeping issues encountered by facility record keepers.
Monitoring Impurities in Pharmaceutical Products – ICH Q3 requirements
This training will discuss regulatory requirements for monitoring of pharmaceutical impurities. It will explain how to monitor impurities in pharmaceutical products as per ICH Q3 A/B requirements and to measure the thresholds to report for regulatory submission.
How to Audit-Proof Your Physician Contracts
This training on healthcare compliance will teach the attendees best practices for conducting a self audit of financial relationships with physicians. It will help you understand the key legal implications of Stark and Federal Anti-Kickback statutes.
Clinical Trial Billing – Building a Compliant Process that Works!
This webinar will show how you can devise a clinical trial billing system/ process to manage the billing of clinical trial charges in compliance with Federal rules and regulations.
FDA Warning Letter – Consent Decree Software Validation
This training on FDA software validation related warning letters will discuss what to do to avoid additional software related compliance issues along with the response steps where the citations that directly or indirectly include automated system.
Building a Sustainable Validation Program from Top to Bottom: One and a Half day In-Person Semina
Companies face many common issues or confusions that arise while creating a validation program such as :
Though company has expertise in process validation but never quite able to keep up with facility and equipment changes requiring never ending equipment qualification (IQ, OQ, PQ)
Medical Device – QSR Compliant Product Development Process: One and half day In-person Seminar
Integrating the requirements of 21 CFR 820 into a product development process is challenging. Done poorly, it drags down the design process and puts you a
Risk based software verification – ISO14971 and IEC62304
Get trained on how to define the residual risk of medical device and how to streamline the software verification process by employing a risk based approach. You will learn Learn the best practices to ensure compliance with ISO14971 and IEC62304 regulations.
Regulatory Compliance for Dietary Supplements in the US, EU and Canada: 2-day In-person Seminar
A growing public demand for supplements has resulted in a flurry of companies creating and marketing dietary supplements in the United States, EU and Canada. With the regulatory authorities beginning to take a stronger stance on enforcement of regulatory policies, procedures and GMP compliance, it is important for companies to verify that their products comply with the latest regulations and provisions if they plan to market Supplements in these countries.
Laboratory Informatics Weekly Update – Volume 12, Issue 2
January 15, 2014 Laboratory Informatics Weekly Update Volume 12, Issue 2 In This Issue SLAS 2014 Don't Miss SLAS2014 January 18-22 SLAS2014 will feature all the great scientific education, programming, intelligent network building and new products and services you have come to expect from SLAS. Make plans to join us in San Diego, CA, January 18-22! Check out SLAS2014.org for the latest event details as they are announced. http://www.slas2014.org/mediapartner Bid / RFP / RFI Opportunities 01/13/2014 - Pre-Solicitation Notice - Laboratory Information Management System Furnish all required services to install Laboratory Information Management System (LIMS Support for Pine Bluff Arsenal…NHS Wales Goes Live with InterSystems TrakCare Lab System to Improve and Modernise Pathology Services Across Wales
InterSystems, a global leader in software for connected care, today announced that NHS Wales has successfully completed the first phase of the national roll out of InterSystems TrakCare® Lab, a comprehensive, multidisciplinary laboratory information management system (LIMS). The first phase of the implementation, covering all four labs in the Hywel Dda Health Board, is a major step in one of the largest and most complex pathology modernisation programmes in the western health economy.
PepTalk
Year-over-year PepTalk: The Protein Science Weekcontinues to draw leaders of biotherapeutics from industry and academia pioneering the evolution of biologics. The international delegation is comprised of over 1,200 participants from 20+ countries.
Pre-Solicitation Notice – Laboratory Information Management System
Furnish all required services to install Laboratory Information Management System (LIMS Support for Pine Bluff ArsenalUnderstanding Disinfectant Qualification Studies – How to avoid errors
This 90-minute webinar on Disinfectant Qualification Studies will teach you disinfectant testing methodologies, provide examples of disinfectant efficacy tests and show how to troubleshoot problems related to disinfectant efficacy testing.
CLC bio and Korilog Release KLAST Software Plug-in for Fast, Accurate Sequence Similarity Search in Next-Generation Sequencing
CLC bio, a QIAGEN company (NASDAQ:QGEN)(FWB:QIA), today announced in collaboration with Korilog the release of the KLAST plug-in for CLC Genomics Workbench and CLC Main Workbench to accelerate the analysis of data from next-generation sequencing (NGS).
Eyelit Releases Version 5.1 of Its Award-Winning Manufacturing Execution (MES) Software Suite
Eyelit Inc., a manufacturing software provider for visibility, control, and coordination of manufacturing operations for the aerospace & defense, discrete electronics, life sciences, MEMS, semiconductor, and photovoltaic (solar) industries, announced today the general availability of version 5.1 of its Eyelit Manufacturing™ suite of software.
MolecularHealth Partners with GATC Biotech for Genetic Sequencing Technology and Expertise
MolecularHealth announced a unique agreement today withGATC Biotech, a global leading DNA sequencing service provider. GATC Biotech will provide protocols, support and extensive training of MolecularHealth’s laboratory staff. Additionally, MolecularHealth will use GATC Biotech’s LIMS (Laboratory Information Management System) in its newly opened clinical lab.
RFI to implement a laboratory information management system in Mozambique
This RFI solicits interest from qualified information technology software providers to implement a laboratory information management system in two sites. One site is the Nampula Central Hospital Laboratory which has multiple laboratory units. The second site is Jose Macamo Hospital Laboratory in Maputo, a district level hospital. This RFI solicits interest from qualified information technology software providers to implement a laboratory information management system in two sites. One site is the Nampula Central Hospital Laboratory which has multiple laboratory units. The second site is Jose Macamo Hospital Laboratory in Maputo, a district level hospital.Understanding FDA and Avoiding Inspections Leading to Warning Letters, Seizures, Injunctions and Prosecutions
Every company regulated by the U.S. FDA establishes procedures, practices and an internal monitoring system all designed to both meet the regulations and manage inspections. However, many are surprised by Warning letters or more serious actions. Regardless of whether your company has been on the receiving side of a regulatory action or not, this course will help you in have better Quality systems, effectively managing and responding to FDA inspections.
Join RURO at SLAS 2014 – Society for Laboratory Automation and Screening, January 18-22, 2014 – San Diego, California
See RURO solutions at SLAS 2014 – Society for Laboratory Automation and Screening.
RURO Booth # 1414
RURO Booth # 1414
