AI HR Solutions: Top Networking LinkedIn Groups for LinkedIn Hiring Excellence in 2026

NABL Provides accreditation services to testing and calibration laboratories in accordance with ISO/IEC 17025 ‘General Requirements for the Competence of Testing and Calibration Laboratories’ and ISO 15189 for ‘Medical laboratories -- Requirements for quality and competence’. The accreditation to Proficiency testing providers is based on ISO/IEC 17043 “Conformity assessment -- General requirements for proficiency testing” and to reference material producers based on ISO 17034 “General requirements for the competence of reference material producers”. NABL offers accreditation services in a non-discriminatory manner. NABL has established its accreditation system in accordance with ISO/ IEC 17011. NABL has Mutual Recognition Arrangements (MRAs) with International Laboratory Accreditation Cooperation (ILAC) and Asia Pacific Accreditation Cooperation (APAC).

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American Medical Laboratories, or “AM LABS”, is America’s number one fungus, mold, mycotoxin, and mycobacterium testing resource laboratory for pinpointing exposure to fungus, mold, mycotoxins, and mycobacterium in the human body. AM Labs helps people link the exposure of toxic compounds in their environments, i.e. fungus, mold, mycotoxins and bacteria to the direct causation of disease within the human body. The right tests can prove that you did contract a fungus, mold or bacteriological related illness from a contaminated environment such as your home, place of employment or school. Mold Sickness is real and is in epidemic proportion within the United States. The sad part is 99% of the time it is misdiagnosed as a mystery illness, or put off as something else. Unless you get the right tests you’ll never know what is in your body .

Our broad base area of expertise includes Agriculture & Food, Bank & Financial Institutions, Commercial Business Services, Chemical Manufacturing, Defense Production, Government & Law Enforcement, Hospitality & Entertainment, Civil Aviation &, Healthcare & Pharmaceutical, Medical Centers & Research Laboratories, Telecommunications, University Campuses & Educational Institutions, Power Plants, Pipelines, Gas & Oil,Utilities, and many more government and industry critical infrastructure sectors.

This group is for companies who have or are starting a Workplace Drug and Alcohol program and service agents. Service agents range from: the Designated Employer Representatives (DER), supervisions, Third Party Administrators/ Consortiums, Certified Professional Collectors, Breath Alcohol Technicians, Alcohol Screening Test Technicians, Certified, Medical Review Officers, Medical Review Assistants, and Substance Abuse Professionals. This group is also for employers who plan on implementing or need questions answered about a Drug-Free Workplace Program(s). This group is a group which will share information about Drug and alcohol in the workplace- so everyone can learn from each other.

N-of-One—On the Leading Edge of a Revolution in Cancer Care The treatment of cancer is in the midst of a revolution fueled by remarkable new advances in understanding the genetics and molecular biology of cancer. Central to these advances is the discovery that each patient's cancer has a specific genetic and molecular signature that may dramatically affect how it will respond to different treatments. This discovery has opened the door to a new approach to cancer treatment called molecular targeted therapy, which targets the specific genetic and molecular abnormalities responsible for the development and growth of a patient's cancer. N-of-One harnesses this emerging science with an entirely new model of cancer care. Our team works with a network of state-of-the-art diagnostic laboratories, leading-edge research institutions, and top cancer experts to analyze each patient's tumor and, based on this information, identify the most advanced and effective treatment strategies available. N-of-One—Making It Personal Our company name—N-of-One—reflects our personalized strategy for cancer treatment. Standard treatment protocols focus on clinical results obtained from the study of large populations of relatively unselected patients (an "n" of many). In contrast, N-of-One focuses on diagnosis and treatment strategies tailored to each individual (an "n" of one), understanding as much as possible about that person's disease at the most fundamental level. Based on sophisticated genetic and molecular analyses of a patient's tumor, N-of-One brings to light information that helps patients and their physicians make the most-informed decisions. N-of-One—Keeping It Independent and Unbiased To serve cancer patients and their medical team with integrity, we do not profit from any laboratory testing, clinical trials, or referrals to cancer centers or members of our expert network.

Medical laboratory technicians work in hospital and private laboratories (clinical or research) or physician office labs. At career entry, the MLT will be able to perform routine clinical laboratory tests done in hematology, chemistry, immunohematology, microbiology, immunology and coagulation. He/she will have gained basic laboratory skills required for entry-level positions in these and other emerging laboratory fields, such as molecular diagnostics. The responsibilities of the MLT include: Decisions concerning sample collection and handling Daily instrument maintenance and quality control SampleCollection and interpretation of data Maintenance of accurate records and reporting of data Knowledge of critical values

Connect with professionals in this LinkedIn group to expand your network and discover new opportunities.

Connect with professionals in this LinkedIn group to expand your network and discover new opportunities.

This group will serve as an information site to guide all mobile laboratories performing under the Clinical Laboratory Improvement Amendment (CLIA) Certificate of Waiver testing, as they are not exempt from CLIA regulations. Testing personnel must be trained, records maintained and testing sites must establish a permit announcing/un-announcing on-site inspection by CMS representatives, if randomly surveyed. This group is intended to function as a network to openly discuss compliance requirements with Federal, State and/or City requirements; Information on how to obtain licenses, permits, among other requirements necessary prior to a Point of Care Testing (POCT); Address recommended components of POCT Quality Assurance & Quality Control policies for FDA approved medical devices, as well as Good Lab Practices (GLP) to assure compliance with OSHA, HIPAA, and other agencies. This forum will serve all clinical and non-clinical personnel which includes, but are not limited to pathologists, directors, managers, consultants, medical device vendors, testing personnel and many others. This will also provide great resource for a company looking to contract with mobile laboratories. It will increase the company’s knowledge on what compliance standard requirements need to be met prior to their wellness screening activities.