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Intronix wins US regulatory clearance for its Myoguide device with assistance from Emergo Group

GenASIs Scan & Analysis cleared for FISH Detection and Analysis of chromosomal abnormalities in urine specimens

This seminar will discuss strategies and present examples on how to transfer analytical methods most efficiently

Delegates now have the option to choose from 3 moderated breakout discussion groups at this conference that is set for February 21-23, San Francisco, CA (part of CHI's Molecular Med TRI-CON 2012).

Dermaroller ® Warns: FDA does not approve the reuse of Single-Use Only medical micro-needling devices.

CHI’s Oncology Clinical Trials conference will highlight three Xalkori case studies by Pfizers’ Hakan Sakul, Ph.D., Keith Wilner, Ph.D., and Erling Thor Donnelly, Ph.D., R.A.C. This conference is part of the Molecular Medicine Tri-Conference.

CHI’s Oncology Clinical Trials conference will highlight two case studies by Seattle Genetics’ Eric Sievers, M.D., Vice President, Clinical Affairs, and Elaine S. Waller, Pharm.D., M.B.A., Senior Vice President, Regulatory Affairs.

CHI’s Oncology Clinical Trials conference will highlight three Zelboraf case studies by Genentech, F. Hoffmann-La Roche, and Roche Molecular Systems. This conference is part of the many program options available at the Tri-Conference.

The manufacturing facility at Wisconsin-based, Integrative Therapeutics, Inc. (ITI®) has received the Therapeutic Goods Administration (TGA) Good Manufacturing Practices (GMP) Certification from Australia.

Trazeback de Colombia Ltda, Partner of ScoringAg, Inc. helping South American Growers to Exporters to get complaint with FDA-FSMA law is a certified provider for all ScoringSystem Inc. databases for all aspects of food and feed traceback.

Former FDA Investigator gives an interview on his experiences inspecting foreign pharmaceutical manufacturers.

Christopher P. Austin, M.D., Scientific Director, NIH Center for Translational Therapeutics, will deliver the keynote presentation at CHI’s Predictive Functional Human Tissue Models conference scheduled on November 17-18, 2011, Boston, MA.

Firm obtains FDA 510(k) clearances with assistance from Emergo Group

3 Boys Farm a Hydroponic Organic Greenhouse operation in Ruskin Florida discovered ScoringAg.com is the only complete database available which works for the requirements of the COOL law, FSMA and FDA 2002 Bioterrorism Law provides full traceability.

Jewish Lawyers network Announces yet another helpline for people having complications with a drug medical device or orthopedic device. Now added to the helplines is a support group for diabetics experiencing side effects from Actos

The Cooley's Anemia Foundation endorses recommendation of Oncologic Drugs Advisory Committee for FDA to approve oral chelator Ferriprox.

Integrative Therapeutics Announces The B.E.S.T. Story Ever Told Winners and Donates $2000 to the American Association of Naturopathic Physicians

The Association of Clinical Researchers and Educators (ACRE) today announced its support for reforms to the Food and Drug Administration’s (FDA) conflict of interest standards.

Injury lawyers Network Announces a vaginal mesh helpline monitered by a female MSW. Injury Lawyer Networks team feels that a female Social worker is in the position to offer help,support and guidance to women facing hope turned to pain and misery

Cigarette companies claiming that it's unconstitutional to require them to advise the public with graphic health warnings seem to forget that this is exactly what happened more than 40 years ago

The Health and Human Services Department has refused to allow the morning-after pill to be sold to girls under 17 without a prescription, reversing an FDA decision.

The CBCD has learned that according to a survey conducted in 2009 by the University of Georgia’s Health Center, only thirty-one percent of sexually active students surveyed had gotten an HPV vaccination.

The "Marketing Pharmaceuticals 2012" conference will take place in Washington, District of Columbia, United States on 16 Feb 2012.

FDA Approves Mitosol® for Immediate Production and Use in Glaucoma Surgery

Pira International is pleased to announce that for 2012, their very successful food contact event, Global Food Contact, will be coming to the USA.

Vaginal Mesh Helpline is on the look out for new updated information. There has been a multi district consolidation of three Vaginal mesh Implants in West Virginia. The vaginal Mesh helpline hears from women daily with horror stories

HIT Consultant Founder Fred Pennic talks with GE Healthcare Senior Marketing Manager of Radiology Lawrence White about the Centricity Radiology Mobile Access Application.

Intronix wins US regulatory clearance for its Myoguide device with assistance from Emergo Group

GenASIs Scan & Analysis cleared for FISH Detection and Analysis of chromosomal abnormalities in urine specimens

This seminar will discuss strategies and present examples on what to train, how much to train and how to document effectiveness

This seminar will discuss strategies and present examples on how to transfer analytical methods most efficiently

Vaginal mesh Helpline is seeing an increase in calls from women In Florida With vaginal mesh Complications, specifically the South Florida Dade, Broward Palm beach Area. This includes Miami thru West Palm Beach

It is well known that document control is a critical requirement for FDA-regulated companies. However, document control can be a time- and paper-consuming process, in which even the simplest of changes requires an inordinate amount of time spent

Many citations by FDA and notified bodies include findings with respect to insufficient information in the Design History File, not following the procedures to make the device as established in the DMR,

SABIC’s Innovative Plastics business today announced that its manufacturing facilities in Campinas, Brazil and Tortuguitas, Argentina, are now certified to produce U.S. Food and Drug Administration (FDA)-compliant and biocompatible resins

Delegates now have the option to choose from 3 moderated breakout discussion groups at this conference that is set for February 21-23, San Francisco, CA (part of CHI's Molecular Med TRI-CON 2012).

Dermaroller ® Warns: FDA does not approve the reuse of Single-Use Only medical micro-needling devices.

Vaginal mesh Helpline listens to women on a Daily basis seeking lawyers who are sensitive to their plight. The biggest complaint is law firms make them feel like a number. The vaginal mesh Helpline is accepting lawyers who meet our criteria.

This seminar will discuss strategies and present examples for qualification of virtual networks and cloud computing

This seminar will discuss how design robustness of analytical methods for easy transfer and to avoid OOS situations

Hundreds of thousands of families affected my defective vaginal mesh surgeries. American Husbands find a new resource to help their wives, families and relationships.

Students are researching ways to improve Salmonella detection in eggs

The FDA is likely to follow a government-mandated report which recommends that nicotine products designed to substitute for cigarette smoking be subjected to such expensive testing that few companies could afford to market them

The Food & Drug Administration is scheduled to release guidelines for the approval of biosimilars by the end of 2011

EMSL Analytical, Inc. offers a variety of consumer products testing, including bisphenol-A analysis

Bootstrap America's Sophia Vander looks at the dangers of genetically engineered foods.

This 90 minute webinar will help you gain a detailed overview of ICH GMPs and the nuances and differences between requirements in the US, EU and Japan. It will help prepare you for regulatory inspections in these countries.

This presentation will provide an understanding of how to get a device requiring a 510(k) submission to market quickly. Knowing when and how to properly submit a 510(k) for a device or change to a device is critical to a company's regulatory

CHI’s Oncology Clinical Trials conference will highlight three Xalkori case studies by Pfizers’ Hakan Sakul, Ph.D., Keith Wilner, Ph.D., and Erling Thor Donnelly, Ph.D., R.A.C. This conference is part of the Molecular Medicine Tri-Conference.

EMSL Analytical, Inc. provides quality Salmonella testing services for pet food products

CHI’s Oncology Clinical Trials conference will highlight two case studies by Seattle Genetics’ Eric Sievers, M.D., Vice President, Clinical Affairs, and Elaine S. Waller, Pharm.D., M.B.A., Senior Vice President, Regulatory Affairs.

More than 96% of tobacco retailers inspected by federal contractors in 38 states were found to be in compliance with new tobacco regulations designed to prevent the sale of tobacco products to minors, according to a report issued by the (FDA) today.

CHI’s Oncology Clinical Trials conference will highlight three Zelboraf case studies by Genentech, F. Hoffmann-La Roche, and Roche Molecular Systems. This conference is part of the many program options available at the Tri-Conference.

EMSL Analytical, Inc. offers microbiological testing services for cosmetic and personal care products

EMSL Analytical, Inc. tests for Pseudomonas luteola and other bacteria in cosmetics and personal care products.

A new white paper detailing the new scope of reusable medical device cleaning validations is available free from Microtest Laboratories.

EMSL Analytical, Inc. offers phthalates testing services for bottled water to ensure compliance

This seminar will present strategies for suppliers to maximize business and for users to minimize validation cost.

The manufacturing facility at Wisconsin-based, Integrative Therapeutics, Inc. (ITI®) has received the Therapeutic Goods Administration (TGA) Good Manufacturing Practices (GMP) Certification from Australia.

An investigation for shareholders of Jazz Pharmaceuticals, Inc. (NASDAQ: JAZZ) over possible breaches of fiduciary duties was announced and NASDAQ:JAZZ stockholders should contact the Shareholders Foundation at mail@shareholdersfoundation.com

This seminar will discuss how regulated user firms can reduce validation costs and how suppliers can increase business

EMSL Analytical, Inc. tests for Salmonella in food products

Should genetically modified food be labeled accordingly? ...this is a raging question that is sweeping large parts of the USA at the moment. Protesters in large numbers agitated in front of the White House a few days ago.

EMSL Analytical, an FDA-registered lab, tests pharmaceuticals in its consumer products division

Dr. Acheson speaks about the Food Safety Modernization Act at Client Connect

EMSL Analytical, Inc. offers food testing services

Trazeback de Colombia Ltda, Partner of ScoringAg, Inc. helping South American Growers to Exporters to get complaint with FDA-FSMA law is a certified provider for all ScoringSystem Inc. databases for all aspects of food and feed traceback.

Visiongain predicts that the global neuromodulation devices market will be worth $11.61bn by 2021. The market generated sales of $2.70bn in 2010, according to Neuromodulation Devices: World Market Prospects 2011-2021, published in October 2011.

Former FDA Investigator gives an interview on his experiences inspecting foreign pharmaceutical manufacturers.

Barnett International announced today the launch of nineteen new in-person and web-based courses. These new courses were added to further serve the constantly evolving training and educational needs of global clinical research professionals today.