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    THIS WEBINAR IS INTENDED TO HELP YOU ADEQUATELY IM 9493 - Webinar On Good Clinical Practices (GCP)

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    Website https://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?id=FDB1517 | Edit Freely

    Category Food, Drugs & Biologics

    Deadline: June 22, 2015 | Date: May 21, 9493

    Venue/Country: Mississauga, Canada

    Updated: 2015-05-21 16:07:35 (GMT+9)

    Call For Papers - CFP

    Description :

    This webinar is intended to help you adequately implement Good Clinical Practices (GCP) including documentation requirements during clinical trials for both drugs and medical devices.

    To adequately implement GCPs, there are a set of standard operating procedures (SOPs) to be established and maintained at any given facility, to the extent applicable, as a sponsor, clinical investigators, monitors, and CROs, etc.

    GCP requirements including documentation requirements (a set of SOPs) with key elements to be contained in the SOP will be discussed.

    In this 60-min webinar, you will have unparalleled opportunities to bring great value and benefits to your organization and to greatly improve your GCPs with increased awareness of the needs - sustainable compliance and patient safety.

    Areas Covered in the Session :

    Laws and Regulations

    Definitions

    Clinical Trials and Requirements

    Regulatory Requirements for INDs and IDEs.

    Duties and Responsibilities for Clinical Investigators (CI), Institutional Review Boards (IRBs), Sponsors and Monitors, and Contract Research Organizations (CROs)

    ICH-GCP Guidelines

    ISO 14155

    List of SOPs and Adequate Documentation

    Key Elements in the SOPs

    Common GCP Deficiencies in EU and US

    Enforcement Actions

    Lessons Learned

    Who Will Benefit:

    Clinical Affairs

    Regulatory Affairs

    Quality Assurance

    Research & Development

    Consultants

    Contractors/Subcontractors

    Senior Management

    Anyone Interested in the Topic

    Price tags:

    Live

    Single Live : For One Participant

    $ 249

    Corporate Live : For Max. 10 Participants

    $ 899

    Recording

    Single REC : For One Participant - Unlimited Access for 6 Months

    $ 299

    For more information and enquiries contact us at

    Compliance Trainings

    5939 Candlebrook Ct, Mississauga, ON L5V 2V5, Canada

    Customer Support : #416-915-4458

    Email : support@compliancetrainings.com


    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.