Current California Clinical Laboratory Laws


Book Description

An essential reference of current California clinical laboratory laws, including new laws taking effect in January, 2013. This book provides an easily accessible, comprehensive, single source of current law for lab directors, lab managers, hospital compliance officers, and lab supervisors. Updated periodically to keep abreast of changes in California statutes and regulations affecting clinical laboratories. While California clinical lab laws are primarily found in the California Business and Professions Code and Title 17 of the California Code of Regulations, this book also contains current and newly enacted laws that the authors feel may be of interest to clinical laboratories that are found in other codes as well.




Current California Clinical Laboratory Laws


Book Description

A laboratory bench reference of current California clinical laboratory laws, aimed at providing an easily accessible, single source of current law for lab directors, lab managers, hospital compliance officers, and lab supervisors. Updated in January 2012, with public health Laboratory laws, infectious disease reporting Laws, and an expanded index. Updated periodically to keep abreast of changes in California statutes and regulations affecting clinical laboratories. While California clinical lab laws are primarily found in the California Business and Professions Code and Title 17 of the California Code of Regulations, this book also contains current and newly enacted laws that the authors feel may be of interest to clinical laboratories that are found in other codes as well.




Returning Individual Research Results to Participants


Book Description

When is it appropriate to return individual research results to participants? The immense interest in this question has been fostered by the growing movement toward greater transparency and participant engagement in the research enterprise. Yet, the risks of returning individual research resultsâ€"such as results with unknown validityâ€"and the associated burdens on the research enterprise are competing considerations. Returning Individual Research Results to Participants reviews the current evidence on the benefits, harms, and costs of returning individual research results, while also considering the ethical, social, operational, and regulatory aspects of the practice. This report includes 12 recommendations directed to various stakeholdersâ€"investigators, sponsors, research institutions, institutional review boards (IRBs), regulators, and participantsâ€"and are designed to help (1) support decision making regarding the return of results on a study-by-study basis, (2) promote high-quality individual research results, (3) foster participant understanding of individual research results, and (4) revise and harmonize current regulations.







Law in the Laboratory


Book Description

The National Institutes of Health and the National Science Foundation together fund more than $40 billon of research annually in the United States and around the globe. These large public expenditures come with strings, including a complex set of laws and guidelines that regulate how scientists may use NIH and NSF funds, how federally funded research may be conducted, and who may have access to or own the product of the research. Until now, researchers have had little instruction on the nature of these laws and how they work. But now, with Robert P. Charrow’s Law in the Laboratory, they have a readable and entertaining introduction to the major ethical and legal considerations pertaining to research under the aegis of federal science funding. For any academic whose position is grant funded, or for any faculty involved in securing grants, this book will be an essential reference manual. And for those who want to learn how federal legislation and regulations affect laboratory research, Charrow’s primer will shed light on the often obscured intersection of government and science.










Good Clinical, Laboratory and Manufacturing Practices


Book Description

Quality assurance and good laboratory practices are becoming essential knowledge for professionals in all sorts of industries. This includes internal and external audit procedures for compliance with the requirements of good clinical, laboratory and manufacturing practices. Spanning chemical, cosmetic and manufacturing industries, Good Clinical, Laboratory and Manufacturing Practices: Techniques for the QA professional is aimed at: chemists, clinicians, ecotoxicologists, operation managers, pharmaceutical process managers, quality assurance officers, technicians and toxicologists. In addition sections on harmonisation of quality systems will be of value to safety, health and environment advisors. This comprehensive and high level reference will be an indispensable guide to research laboratories in academia and industry. Additional training material is also included.