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    Medical Foods:Practical Tips to Meet FDA Requirements for Claims and Quality

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    Website http://www.onlinecompliancepanel.com?expDate=Ourglocal | Want to Edit it Edit Freely

    Category 508 compliance; act compliance; fda compliance; ada compliance; advisor compliance; argent software pci compliance; certificate of compliance; code compliance; compliance; compliance audit; compliance checklist; compliance issues; compliance jobs; compliance management; compliance manager; compliance manual; compliance monitoring; compliance monitoring ppt; compliance officer; compliance plan; compliance plans; compliance program; compliance software; compliance solutions; compliance testing; compliance training; compliance with; contract compliance; corporate compliance; email compliance; environmental compliance; export compliance; health care compliance; healthcare compliance; hipaa compliance; hippa compliance; investment advisor compliance; medical compliance; medication compliance; non compliance; osha compliance; osha compliance training; pci compliance; policy compliance; regulatory compliance; rohs compliance; safety compliance; sarbanes oxley compliance; security compliance; sox compliance; tax comp

    Deadline: June 10, 2014 | Date: June 10, 2014

    Venue/Country: 38868 Salmon Ter, Fremont, U.S.A

    Updated: 2014-04-17 18:39:04 (GMT+9)

    Call For Papers - CFP

    Instructor: Mukesh Kumar

    Description:

    Medical foods play an important role in the management of patients with special dietary restrictions and needs. The designation of medical food by FDA implies special handling, labeling, distribution and manufacturing requirements. Manufacturers are usually worried about meeting all of FDA's complex requirements for such products. This seminar will discuss the regulatory processes to designate and market a product as medical food. Common issues with FDA compliance will be discussed using case studies and potential solutions will be discussed.

    Why Should you Attend:

    Medical foods designation comes with its own set of regulatory responsibilities. FDA expects manufacturers to self-assure compliance status and reserves the option to audit all aspects of the manufacturing, labeling and distribution as it deems necessary. This seminar fills the gap in knowledge in terms of the FDA expectations from medical foods and way to address common deficiencies. The case studies discussed will further highlight potential audit issues, training requirements, good manufacturing practices for medical foods, and marketing issues.

    Objectives of the Presentation:

    Current FDA accepted definition of medical foods and functions foods.

    Medical foods and dietary supplements

    Good manufacturing practices for medical foods.

    Best practices for marketing and distribution.

    Review of case-studies from unsuccessful and successful marketing of medical foods.

    Practical tips for training of sales and marketing teams in medical foods.

    Regulatory strategies for designating dietary supplements and medical foods.

    Who can Benefit:

    This webinar will provide valuable information to:

    Manufacturers of medical foods

    Physicians and Hospital Personnel

    Dietary Supplement Manufacturers

    Marketing and Advertising Professionals

    Regulatory Affairs Professionals, Research Analysts

    http://www.onlinecompliancepanel.com/ecommerce/webinar/~product_id=500296?expDate=Ourglocal


    Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
    Disclaimer: ourGlocal is an open academical resource system, which anyone can edit or update. Usually, journal information updated by us, journal managers or others. So the information is old or wrong now. Specially, impact factor is changing every year. Even it was correct when updated, it may have been changed now. So please go to Thomson Reuters to confirm latest value about Journal impact factor.