Medical Devices Regulations 1994

List Of Statutory Instruments Of The United Kingdom, 1994 News

After His degree (1982) Became technical manager of a cosmetic company and after Launched (1989) His own company named NEOVITA.
With growing activity as consultant Became technical manager for other companies.

Launched in 1999 the firm Dermopatch for the production of patches for cosmetic treatment and delivery.
He cooperated with some very important world cosmetic companies, Universities and specialized manufacturers Gaining a great experience.

He left in 2005 and developed new products for other companies, Among others the application of a new technology delivery from fabrics (medical and cosmetic), Developing a medical device for the diabetic foot pathology

At University published in duplicated lecture notes, after he published articles in various fields and different specialized and scientific journals, some specialized chapters in books (regulatory and delivery systems), and congress presentations.

Board member of the Italian Society of Cosmetics Chemists and the Scientific Affairs Committee. Chairman of International Conference of IFSCC - Florence in 2005.

From 1987 is as scientific consultant for the law court
He served two years in the army (artillery regiment lieutenant at Horse-Milan), now has a role in reserve being invited as expert in the field of CBRN at NRDC-ITA (NATO Rapid Deployable Corps - Italy) NATO Headquarters-Solbiate Olona

He Has Been member of MENSA International and Lions

Specializations regulatory validation cosmetics, medical devices, quality compliance, new products development, relationships with control authorities, import-export cosmetics, medical devices, reach

1994 U.S. government review shows mixed bag; environmental issues, medical device regulations and international trade top INDA's agenda. (Association ... An article from: Nonwovens Industry
Book (Rodman Publications, Inc.)
2006-02-20 17:02:02 by Bioseeker

8 years in biotech

I've been working consistently in the biotech field, after a BA in Psychobiology for 8 years.
-Regulatory Affairs deals with getting FDA approval of new drugs and medical devices.
I went to the Biospace job fair last month but haven't got any calls. I'm wondering if its b/c I currently reside in LA. I'm thinking of moving down there and looking for something fast thru a temp agency. Any advice?

2009-01-11 15:13:59 by windshadow

More from hsi

Last month, a group of FDA scientists sent an SOS to Representative John D. Dingell, chairman of the House Committee on Energy and Commerce. The letter calls for "urgent intervention" due to "serious misconduct" by managers of the Center for Devices and Radiological Health (CDRH) – the FDA division that oversees everything from imaging equipment to breast implants.
So what constitutes "serious misconduct"?
Here's how the scientists put it: "There is extensive documentary evidence that managers at CDRH have corrupted and interfered with the scientific review of medical devices

2007-09-08 13:08:25 by -------

Chip implants shown to cause cancer, a

-
"When the U.S. Food and Drug Administration approved implanting microchips in humans, the manufacturer said it would save lives, letting doctors scan the tiny transponders to access patients' medical records almost instantly. The FDA found "reasonable assurance" the device was safe, and a sub-agency even called it one of 2005's top "innovative technologies."
But neither the company nor the regulators publicly mentioned this: A series of veterinary and toxicology studies, dating to the mid-1990s, stated that chip implants had "induced" malignant tumors in some lab mice and rats

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Implementing FDA Quality System Regulations
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The Medical Devices Regulations 1994 (Statutory instruments: 1994: 3017)
Book (Stationery Office Books)
Guidelines to the European Communities (Medical Devices) Regulations, 1994, for manufacturers of custom-made medical devices
Book (Medical Devices Section of the Department of Health and Children)
Federal preemption of medical device tort claims; not what Congress (or the doctor) ordered.: An article from: Trial
Book (Association of Trial Lawyers of America)
Hudson Inst Health Care Reform, Regulation, & Innovation in the Medical Device Industry: A Study of Competitiveness in a Vital U.S. Industry
Book (Hudson Inst)
  • Used Book in Good Condition

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