This clinical compliance training will help attendees understand how they can develop and implement a Quality Assurance (QA) program at their clinical research site that ensures the staff are properly trained and that the research is carried out in accordance with regulatory expectations.Why Should You Attend:Is your site carrying out clinical research in accordance with regulatory expectations? You have training requirements for investigators and coordinators, is that enough? Is it worthwhile…See More
This training on Medical Device Reporting (MDR) requirements will provide attendees the best practices for implementing an adverse event reporting system for medical devices including in vitro diagnostic devices (IVDs).Why Should You Attend:In the United States, since December 13, 1984, the Food and Drug Administration (FDA) Medical Device Reporting (MDR) regulations have required firms who have received complaints of device malfunctions, serious injuries or deaths associated with medical…See More
This training on Organic Labeling & Marketing will help the attendees understand the requirements of the USDA National Organic Program including the expectations in the agriculture sector. It will highlight the agricultural methods used to grow food and approved methods that integrate cultural, biological and mechanical practices.Why Should You Attend:It seems wherever you go organic labels, advertisements and marketing claims are becoming more and more prevalent. There is a pressure on…See More
How is everything with you, I picked interest on you after going through your short profile and deemed it necessary to write you immediately. I have something very vital to disclose to you, but I found it difficult to express myself here, since it's a public site.Could you please get back to me on:( email@example.com ) for the full details.