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Joseph Potocny Oceanside, California
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Federal Register: Use of International Standard ISO-10993, 'Biological Evaluation of Medical Devices Part 1: Evaluation and by FDA Standard ISO-10993, `Biological Evaluation of Medical Devices Part 1: Evaluation and Testing.' 'FDA has developed this guidance document to assist industry in...
UK General Medical Council: "Dr. Andrew Wakefield's Name Should Be Erased From the Medical Register" by Kim S. Patient Expert of patients. The Panel considered the conduct of Dr Wakefield whilst he was registered as a medical... from the standards of a registered medical practitioner and concluded that these amounted individually...
The Cisco Medical Clinic – Company Medical Assistance and Consults On Site by Medical Quack Patient ExpertHealth Maven health clinic looks more like a pampering day spa than a medical facility for the company's employees... and medical information before entering the exam room. Comfortable padded exam tables, a choice of robes or...
UK General Medical Council: "Professor John Walker-Smith's Name Should Be Erased from the Medical Register" by Kim S. Patient Expert were serious departures from the standards of a registered medical practitioner and concluded that Professor... between research medicine, with its prime purpose of testing an hypothesis, clinical medical practice undertaken...
1-2 Associate (Assistant) Professors in Medical Science Communication and/or Medical Science Heritage Production by Thomas S. Patient Expert  (alternatively Assistant Professor). As readers of this blog probably knows, Medical Museion is an integrated... and “Associate (Assistant) Professor at Medical Museion” to: The Faculty of Health Sciences University...
Federal Register: Guidances for Industry and Food and Drug Administration Staff: Computer-Assisted Detection Devices Applied to by FDA The Food and Drug Administration (FDA) is announcing the availability of two related guidance documents.
Federal Register: Medical Devices; Hematology and Pathology Devices; Classification of Early Growth Response 1 Gene Fluorescence by FDA The FDA is classifying early growth response 1 (EGR1) gene fluorescence in-situ hybridization (FISH) test system for specimen characterization into class II (special controls). The special controls...
Federal Register: Microbiology Devices Panel of the Medical Devices Advisory by FDA This notice announces a forthcoming meeting of a public advisory committee of the Food and Drug Administration (FDA). The meeting will be open to the public.
Federal Register: Medical Devices; Immunology and Microbiology Devices; Classification of John Cunningham Virus Serological Reag by FDA The FDA is classifying John Cunningham Virus (JCV) serological reagents into class II (special controls). The Agency is classifying the device into class II (special controls) in order to provide a reasonable assurance of sa
Federal Register: Medical Devices; Immunology and Microbiology Devices; Classification of Dengue Virus Serological Reagents by FDA The FDA is classifying dengue virus serological reagents into class II (special controls). The special controls that will apply to the device are identified in this order, and the codified language for the dengue serological

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