• Steven S. Kuwahara Recorded
    View Anytime
    Duration:90 Minutes
    Price: $190.00
    by: Steven S. Kuwahara
    GMP Expectations for Products Used in Early Phase IND Studies
    FDA issued a guidance document covering GMP requirements for Phase 1 products. These guidelines remove some of the problems that are encountered with early phase products and are in addition to those that cover the CMC sections for IND submissions at Phase 1.

  • Steven S. Kuwahara Recorded
    View Anytime
    Duration:90 Minutes
    Price: $190.00
    by: Steven S. Kuwahara
    Auditing Analytical Laboratories for FDA Compliance
    Auditing analytical laboratories can be complex because of the preparation that is often required. All of the GMP rules do not apply to the laboratory; while there may be additional requirements depending upon the type of testing that is being conducted. In many cases, the laboratory itself may not understand what regulations apply to the work that is being conducted.

  • Steven S. Kuwahara Recorded
    View Anytime
    Duration:75 Minutes
    Price: $190.00
    by: Steven S. Kuwahara
    GMP Expectations for Products Used in Early Phase IND Studies
    FDA issued a guidance document covering GMP requirements for Phase 1 products. These guidelines remove some of the problems that are encountered with early phase products and are in addition to those that cover the CMC sections for IND submissions at Phase 1.

  • Steven S. Kuwahara Recorded
    View Anytime
    Duration:90 Minutes
    Price: $190.00
    by: Steven S. Kuwahara
    Auditing Analytical Laboratories for FDA Compliance
    Auditing analytical laboratories can be complex because of the preparation that is often required. All of the GMP rules do not apply to the laboratory; while there may be additional requirements depending upon the type of testing that is being conducted. In many cases, the laboratory itself may not understand what regulations apply to the work that is being conducted.

  • Steven S. Kuwahara Recorded
    View Anytime
    Duration:90 Minutes
    Price: $190.00
    by: Steven S. Kuwahara
    Auditing Analytical Laboratories for FDA Compliance
    Auditing analytical laboratories can be complex because of the preparation that is often required. All of the GMP rules do not apply to the laboratory; while there may be additional requirements depending upon the type of testing that is being conducted. In many cases, the laboratory itself may not understand what regulations apply to the work that is being conducted.

  • Steven S. Kuwahara Recorded
    View Anytime
    Duration:75 Minutes
    Price: $190.00
    by: Steven S. Kuwahara
    GMP Expectations for Products Used in Early Phase IND Studies
    FDA issued a guidance document covering GMP requirements for Phase 1 products. These guidelines remove some of the problems that are encountered with early phase products and are in addition to those that cover the CMC sections for IND submissions at Phase 1.

  • Steven S. Kuwahara Recorded
    View Anytime
    Duration:90 Minutes
    Price: $190.00
    by: Steven S. Kuwahara
    Auditing Analytical Laboratories for FDA Compliance
    Auditing analytical laboratories can be complex because of the preparation that is often required. All of the GMP rules do not apply to the laboratory; while there may be additional requirements depending upon the type of testing that is being conducted. In many cases, the laboratory itself may not understand what regulations apply to the work that is being conducted.

  • Steven S. Kuwahara Recorded
    View Anytime
    Duration:90 Minutes
    Price: $190.00
    by: Steven S. Kuwahara
    Auditing Analytical Laboratories for FDA Compliance
    Auditing analytical laboratories can be complex because of the preparation that is often required. All of the GMP rules do not apply to the laboratory; while there may be additional requirements depending upon the type of testing that is being conducted. In many cases, the laboratory itself may not understand what regulations apply to the work that is being conducted.

  • Steven S. Kuwahara Recorded
    View Anytime
    Duration:90 Minutes
    Price: $190.00
    by: Steven S. Kuwahara
    Auditing Analytical Laboratories for FDA Compliance
    Auditing analytical laboratories can be complex because of the preparation that is often required. All of the GMP rules do not apply to the laboratory; while there may be additional requirements depending upon the type of testing that is being conducted. In many cases, the laboratory itself may not understand what regulations apply to the work that is being conducted.

  • Steven S. Kuwahara Recorded
    View Anytime
    Duration:90 Minutes
    Price: $190.00
    by: Steven S. Kuwahara
    Auditing Analytical Laboratories for FDA Compliance
    Auditing analytical laboratories can be complex because of the preparation that is often required. All of the GMP rules do not apply to the laboratory; while there may be additional requirements depending upon the type of testing that is being conducted. In many cases, the laboratory itself may not understand what regulations apply to the work that is being conducted.

  • Steven S. Kuwahara Recorded
    View Anytime
    Duration:75 Minutes
    Price: $190.00
    by: Steven S. Kuwahara
    GMP Expectations for Products Used in Early Phase IND Studies
    FDA issued a guidance document covering GMP requirements for Phase 1 products. These guidelines remove some of the problems that are encountered with early phase products and are in addition to those that cover the CMC sections for IND submissions at Phase 1.

  • Steven S. Kuwahara Recorded
    View Anytime
    Duration:75 Minutes
    Price: $189.00
    by: Steven S. Kuwahara
    GMP Expectations for Products Used in Early Phase IND Studies
    FDA issued a guidance document covering GMP requirements for Phase 1 products. These guidelines remove some of the problems that are encountered with early phase products and are in addition to those that cover the CMC sections for IND submissions at Phase 1.

  • Steven S. Kuwahara Recorded
    View Anytime
    Duration:90 Minutes
    Price: $189.00
    by: Steven S. Kuwahara
    Auditing Analytical Laboratories for FDA Compliance
    Auditing analytical laboratories can be complex because of the preparation that is often required. All of the GMP rules do not apply to the laboratory; while there may be additional requirements depending upon the type of testing that is being conducted. In many cases, the laboratory itself may not understand what regulations apply to the work that is being conducted.

  • Steven S. Kuwahara Recorded
    View Anytime
    Duration:75 Minutes
    Price: $189.00
    by: Steven S. Kuwahara
    GMP Perspectives on Working with Contracting Laboratories
    When working with contract testing laboratories, clients must remember that the responsibility for compliance with the GMP or the GLP ultimately lies with the product sponsor. Even if the contract assignes the responsibility to the contract laboratory, the responsibility for assuring compliance lies with the client. Neither can the contract laboratory assume that the client has complied with their responsibilities.

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