Webinar Search Results : 1 Upcoming webinars found.
Jerry Lanese Friday, August 23, 2019
10:00 AM PDT | 01:00 PM EDT
Duration:90 Minutes
Price: $150.00
by: Jerry Lanese
Analytical Method Validation
An analytical method is a process. The FDA process validation guidance applies to test methods, like all other processes in the pharmaceutical industry. Therefore, the laboratory or laboratories must demonstrate that a test method performs as intended through the method lifecycle.

  • Jerry Lanese Recorded
    View Anytime
    Duration:90 Minutes
    Price: $190.00
    by: Jerry Lanese
    Analytical Method Validation
    An analytical method is a process. The FDA process validation guidance applies to test methods, like all other processes in the pharmaceutical industry. Therefore, the laboratory or laboratories must demonstrate that a test method performs as intended through the method lifecycle.

  • Jerry Lanese Recorded
    View Anytime
    Duration:90 Minutes
    Price: $190.00
    by: Jerry Lanese
    Analytical Method Validation
    An analytical method is a process. The FDA process validation guidance applies to test methods, like all other processes in the pharmaceutical industry. Therefore, the laboratory or laboratories must demonstrate that a test method performs as intended through the method lifecycle.

  • Jerry Lanese Recorded
    View Anytime
    Duration:90 Minutes
    Price: $190.00
    by: Jerry Lanese
    Laboratory Investigation of Out-of-Specification Results
    The objective of this webinar is to develop an understanding of how a compliant laboratory handles the investigation of out-of-specification (OOS) test results and how the laboratory interfaces with other units through the laboratory investigation process. The discussion will be based on the FDA guidance on handling OOS laboratory results.

  • Jerry Lanese Recorded
    View Anytime
    Duration:90 Minutes
    Price: $190.00
    by: Jerry Lanese
    Analytical Method Validation
    An analytical method is a process. The FDA process validation guidance applies to test methods, like all other processes in the pharmaceutical industry. Therefore, the laboratory or laboratories must demonstrate that a test method performs as intended through the method lifecycle.

  • Jerry Lanese Recorded
    View Anytime
    Duration:90 Minutes
    Price: $190.00
    by: Jerry Lanese
    Laboratory Investigation of Out-of-Specification Results
    The objective of this webinar is to develop an understanding of how a compliant laboratory handles the investigation of out-of-specification (OOS) test results and how the laboratory interfaces with other units through the laboratory investigation process. The discussion will be based on the FDA guidance on handling OOS laboratory results.

  • Jerry Lanese Recorded
    View Anytime
    Duration:90 Minutes
    Price: $190.00
    by: Jerry Lanese
    Analytical Method Validation
    An analytical method is a process. The FDA process validation guidance applies to test methods, like all other processes in the pharmaceutical industry. Therefore, the laboratory or laboratories must demonstrate that a test method performs as intended through the method lifecycle.

  • Jerry Lanese Recorded
    View Anytime
    Duration:90 Minutes
    Price: $190.00
    by: Jerry Lanese
    Laboratory Investigation of Out-of-Specification Results
    The objective of this webinar is to develop an understanding of how a compliant laboratory handles the investigation of out-of-specification (OOS) test results and how the laboratory interfaces with other units through the laboratory investigation process. The discussion will be based on the FDA guidance on handling OOS laboratory results.

  • Jerry Lanese Recorded
    View Anytime
    Duration:90 Minutes
    Price: $190.00
    by: Jerry Lanese
    Laboratory Investigation of Out-of-Specification Results
    The objective of this webinar is to develop an understanding of how a compliant laboratory handles the investigation of out-of-specification (OOS) test results and how the laboratory interfaces with other units through the laboratory investigation process. The discussion will be based on the FDA guidance on handling OOS laboratory results.

  • Jerry Lanese Recorded
    View Anytime
    Duration:90 Minutes
    Price: $189.00
    by: Jerry Lanese
    cGMPs in the Quality Control Laboratory
    Since the mid 1980s, the Quality Control Lab oratory has been a prime target for FDA investigators during site inspections. Since that time, investigators have made many 483 observations. Unless the firm reacts very aggressively, the 483 observations will be escalated to Warning Letter citations.

  • Jerry Lanese Recorded
    View Anytime
    Duration:90 Minutes
    Price: $189.00
    by: Jerry Lanese
    Analytical Method Validation
    An analytical method is a process. The FDA process validation guidance applies to test methods, like all other processes in the pharmaceutical industry. Therefore, the laboratory or laboratories must demonstrate that a test method performs as intended through the method lifecycle.

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