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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.

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

MediPurpose also announced that its expanding MediPlus(tm) advanced wound care product portfolio now includes Foam Ag, Comfort Foam Ag and Super Foam Ag dressings

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.

Critical information that dietary supplement manufacturers must know in order to meet the FDA's good manufacturing practices “compliance paradigm” is detailed in a free white paper from Microtest Laboratories.

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

Read about these 3 reasons why you should do your homework on the health industry.

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

Radient Pharmaceuticals a developer and marketer of In Vitro Diagnostic (IVD) cancer tests, today announced it has filed for patent protection for its proprietary Onko-Sure(R) cancer test in Australia and New Zealand.

This seminar will discuss FDA requirements for computer system validation and will go through all steps for implementation.

This seminar will provide more that 20 examples of recent FDA warning letters and give clear recommendations for corrective and preventive actions.

This seminar will provide all information and tools on how to qualify network infrastructure for FDA compliance.

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

This course will describe the regulatory and business requirements for Excel spreadsheets, using examples from FDA recommendations. It will then cover the design and installation of those Excel Spreadsheets, to ensure the integrity of the data,

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.

Complying with GLP regulations can increase the cost of a laboratory up to 30%. Companies or employees either don't know exactly what GLP really means, or what procedures are required and how to implement GLP regulations.

Do you trust the FDA? Sometimes the things they do can affect you in the wrong way. Read up on what to look out for.

Enforcement of HIPAA regulations is being stepped up and new fines and penalties make being ready for an audit in advance essential.

Transportation software provider, IES, Ltd., is the first Ocean AMS service provider to successfully pass the testing requirements for M1 and transmit data to the ACE (Automated Commercial Environment) portal.

Because of severe manipulations of computerized laboratory data by industry FDA inspectors focus on integrity and security of electronic records.This seminar will provide all information on how to demonstrate integrity and security of laboratory data

Visitors to the Interpack 2011 exhibition in Dϋsseldorf were given the opportunity to attend a series of special in-house seminars presented by pharmaceutical freeze dryer manufacturer GEA Lyophil.

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

This webinar provides step by step instructions on how to design and manage a CAPA system that meets and exceeds compliance requirements

FDA-mandated post-market studies are coming. Phase IV studies are likely to be complex in design and large in scale (possibly 500,000 patients per arm), with exacting endpoints, and obligatory. The FDA appears to be abandoning a long-standing policy

This Project Management training for FDA Regulated Companies will show how you can meet key FDA and EU MDD regulatory requirements for the project you manage.