Quality Assurance

Washington – November 02, 2026 -- URAC and Asembia have launched a strategic partnership that gives eligible members of Asembia's Group Purchasing Organization (GPO) access to URAC accreditation programs, educational resources and support. The companies describe the arrangement as a streamlined path to URAC accreditation for specialty pharmacies.

Asembia GPO members gain a direct route to independent accreditation

URAC is an independent nonprofit health care accreditor. Asembia provides group purchasing, patient support, technology, data and distribution solutions to the specialty pharmaceutical industry. The collaboration links Asembia's connected GPO membership with URAC's accreditation programs. The stated aim is to help participating pharmacies strengthen quality, operational performance and patient care delivery.

OSLO – – October 29, 2026 -- Agilyx ASA's analytical lab arcLABS has obtained ISO/IEC 17025:2017 accreditation from the ANSI National Accreditation Board (ANAB), allowing it to issue accredited results for plastics and chemical recycling clients. The company trades on Euronext Oslo Børs (AGLX), Börse Frankfurt (5NQ) and the USOTCQX (AGYXY).

Accredited Certificates of Analysis now cover feedstock, validation and compliance testing

Customers can receive accredited results and Certificates of Analysis for in-scope feedstock characterization, material validation and regulatory compliance testing. ISO/IEC 17025 is the global standard for testing and calibration laboratories. It covers impartiality, method validation, measurement traceability and quality management.

ANAB is the largest accreditation body in North America. Its accreditations are recognized internationally through the ILAC Mutual Recognition Arrangement.

Westborough, Mass. – October 29, 2026 -- KPM Analytics has released UCAL 5, a near-infrared (NIR) calibration platform for SpectraStar XT Series analyzers that checks every calibration against ASTM E1655 and ISO 12099 recommendations as the user works. The patent-pending guided workflow takes users from KPM calibration libraries to a published calibration for their own products in four steps. A 30-day free trial of UCAL 5 Pro is available now to current SpectraStar XT users.

UCAL Insight flags weak calibrations with green, yellow and red marks

UCAL Insight checks whether a calibration has enough samples, how well laboratory values cover the required range, and whether new samples confirm the calibration. Each point is marked green, yellow or red with an explanation. The marks are suggestions, and the user makes the final decision.

Pleasanton – October 16, 2026 -- n6 Tec, Inc. has received ISO 13485:2016 certification from Intertek for its quality management system, covering the manufacture and service of genetic research instrumentation at its Pleasanton, California headquarters.

Certificate 0259003 runs through October 2029

Intertek issued the initial certificate on October 12, 2026. It is valid through October 11, 2029, subject to ongoing surveillance by the certification body.

ISO 13485:2016 is the international quality management standard for organizations that design, manufacture and service medical devices. An independent auditor must verify that documented processes for design controls, supplier management, manufacturing, traceability, corrective and preventive action, and customer feedback exist and are followed.

Boise, Idaho – October 14, 2026 -- Clean Form Nutrition has become the first brand to earn NSF Certified for Sport® certification for a finished product containing NNB Nutrition's Pürest CreatineTM, adding a finished-product check to an ingredient already certified by Informed Choice and tested by two independent laboratories.

Eurofins tests find no quantifiable impurities in three Pürest Creatine lots

In comparative testing by Eurofins, three separate production lots of Pürest CreatineTM were evaluated alongside a premium creatine described as an industry purity benchmark. In all three lots, dicyandiamide (DCD), dihydrotriazine (DHT) and creatinine fell below the laboratory's limits of quantification.

The benchmark sample contained measurable levels of both DCD and creatinine. DHT stayed below the quantification limit in both products. Mérieux NutriSciences has also tested Pürest CreatineTM for creatine manufacturing impurities.

Evansville – October 14, 2026 -- Heart to Heart Hospice's Evansville, Indiana office has received the 2026 Hospice CAHPS Honors Elite designation, the highest recognition level in the Hospice CAHPS Honors program.

Evansville office joins a limited group of top-rated US hospice providers

The distinction places the office among a select group of hospice providers nationwide that have demonstrated outstanding performance and a sustained commitment to care experiences for patients and families.

Elite tier requires beating national benchmarks across multiple care measures

Hospice CAHPS Honors Elite goes beyond high family satisfaction scores. It recognizes agencies that also exceed national performance benchmarks across multiple measures of care. The program is regarded as one of the industry's most respected gauges of hospice quality and patient experience.

Mexico City – September 21, 2026 -- The Association for the Accreditation of Human Research Protection Programs (AAHRPP) has awarded full accreditation to Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán (INCMNSZ), making it the first of Mexico's 13 National Institutes of Health under the Mexican Ministry of Health to reach this status.

INCMNSZ becomes only the second organization in Mexico to earn AAHRPP accreditation, joining a global roster that now exceeds 600 accredited entities. AAHRPP separately confirmed reaccreditation for five additional organizations, underscoring continued renewal activity within its existing accredited network.

Indianapolis – September 17, 2026 -- Crystal Risotti, Senior Manager of Validation in Quality Assurance at CTI, has been named a Pinnacle Professional of the Year by The Inner Circle for her three-decade career in information technology quality assurance and regulatory compliance across pharmaceuticals, medical devices and clinical laboratories.

Risotti built her career from clinical trial lab work in 1990 to enterprise-wide compliance leadership

Risotti entered the pharmaceutical industry in 1990 as a clinical trials laboratory worker before moving through customer service, project management, training and Tier 4 help desk roles. She later specialized in software development life cycle consultation, 21 CFR Part 11 compliance, and electronic quality management system implementation, working remotely from Indianapolis, Indiana while based at CTI's Covington, Kentucky office.

Miami – September 16, 2026 -- BioEdge Research Labs has begun publishing batch-specific Certificates of Analysis (COAs) directly on its product pages, allowing laboratory customers to verify identity and purity data for the exact lot they receive rather than relying on aggregated supplier summaries.

Each lot now carries its own matched documentation

Instead of a single certificate applied across multiple production runs, every vial supplied by the Miami-based company is assigned a lot number tied to a corresponding COA, letting researchers cross-check the physical material against its specific record.

Independent labs handle identity and purity testing

The underlying analysis is conducted by a third-party laboratory rather than BioEdge itself, covering identity verification via mass spectrometry, purity assessment via high-performance liquid chromatography, and contaminant screening.