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    HEALTHCARE TRAINING 2020 - 6-Hour Virtual Seminar on Auditing Analytical Laboratories for FDA Compliance

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    Website https://www.globalcompliancepanel.com/virtual-seminar/6-hour-virtual-seminar-on-auditing-analytical- | Edit Freely

    Category HEALTHCARE TRAINING 2020

    Deadline: August 20, 2020 | Date: August 20, 2020

    Venue/Country: U.S.A

    Updated: 2020-06-29 21:58:24 (GMT+9)

    Call For Papers - CFP

    There are two phases to this topic. The first is auditing itself. Good audits are well structured. They must consider the reasons for the audit, the regulatory requirements, as well as the nature of the laboratory being audited. We will discuss the considerations that must be made when auditing a laboratory. The social interactions that must be expected, the nature of the regulatory requirements and the nature of work that the laboratory performs will be discussed.

    The second phase considers what must be considered during the audit itself. Audits conducted by inexperienced or ignorant auditors are often worthless, wasting the time and money of both the auditors and the laboratory being audited. Auditors who are familiar with laboratory operations are needed as it is easy to be fooled into thinking that a non-compliant laboratory is operating normally. Different types of laboratories will require different auditor/specialists. We will discuss the pitfalls that auditors can fall into, and what questions laboratories may expect to encounter.

    Why you should attend

    It is necessary for a company to know if an analytical laboratory is capable of operating in compliance with GMP or other regulations. This is especially critical if the laboratory is a quality control laboratory whose test results will be used to support the release of a product to the public or to support and application for permission to market a product. The failure of a quality control laboratory to comply with regulations can result in the failure of a request for permission to market a product or a forced recall of a marketed product.

    In extreme cases a revocation of the permission to market a product may be the result. In any case the inability to conform to regulations will result in a loss of confidence in the ability of the manufacturer to produce a product that meets quality and regulatory requirements, and, in turn, lead to a refusal to purchase a product.

    It is critical that the audit of the laboratory be conducted in a professional manner, as a poor audit will waste money and lead to a false confidence in the abilities of the audited laboratory whether it is internal or external to the company.

    Who Will Benefit

    Potential Auditors

    Supervisors who must initiate Audits

    Laboratory Supervisors and Workers

    Quality Assurance and Control Supervisors and Lead Workers

    Supervisory Management who must select Contractors

    Managers

    Directors

    Vice Presidents who Supervise Quality Assurance

    Quality Control

    Regulatory Affairs Groups

    https://www.globalcompliancepanel.com/virtual-seminar/6-hour-virtual-seminar-on-auditing-analytical-laboratories-for-fda-compliance-11495LIVE


    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.