The iQue ® software module for 21 CFR Part 11 ensures next-level iQue ® productivity for regulated laboratories. Designed for speed and actionable results, iQue ® is the instrument of choice ...

See 21 CFR parts 11, 54, 210, 211, 312; the FDA Center for Drug Evaluation and Research; and UAB HRPP PRO121 Procedure to Ensure Handling of Investigational or Unlicensed Test Articles Meets ...

The NMU is 21 CFR Part 11 compliant. The company’s Current Good Manufacturing ... with a rapid turnaround time of three weeks ...

The point-of-care system and regulatory framework will drive ELISA analyzer demand.Wilmington, Delaware, United States, Transparency Market Research, Inc. , Nov. 12, 2024 (GLOBE NEWSWIRE) -- The ELISA ...

Analyses with Vision Air are completely traceable and meet the requirements of the FDA 21 CFR part 11 for the pharmaceutical industry. Vision Air is easy to command. Two clicks is all that is ...

The new director at the FDA overseeing medical devices will confront criticisms about hasty approvals as she ushers in ...

Watlow, a US-based industrial heating manufacturer, will preview its Eurotherm branded Edge Process Management platform at ...

(RTTNews) - Biotechnology company Unicycive Therapeutics, Inc. (UNCY) announced Monday that the U.S. Food and Drug Administration (FDA) has accepted the New Drug Application (NDA) for Oxylanthanum ...

The life sciences industry is embracing the transformative power of artificial intelligence (AI) and automation, leveraging its unmatched advancements in speed, accuracy, and efficiency to ...

Heat and Control, in Booths N-6104 and N-6106 at PACK EXPO International, will display its THS/PH210 Series metal detectors ...