DANIELLE DELUCY

  Add To Cart
Recording
  

FDA Case Scenarios – Best Practices for Managing Inspection Situations

FDB2169
DANIELLE DELUCY

Duration: 75 Minutes

  Add To Cart
Recording
  

How to conduct Annual Product Reviews to achieve GMP Compliance

FDB3164
DANIELLE DELUCY

Duration: 75 Minutes

  Add To Cart
Recording
  

Good Documentation Practices

FDB2866
DANIELLE DELUCY

Duration: 75 Minutes

  Add To Cart
Recording
  

Steam Sterilization Microbiology and Autoclave Performance Qualification

FDB2261
DANIELLE DELUCY

Duration: 75 Minutes

  Add To Cart
Recording
  

Effective Batch Record Review

FDB2469
DANIELLE DELUCY

Duration: 75 Minutes

  Add To Cart
Recording
  

3-Hour Virtual Seminar on Handling OOS Test Results and Completing Robust Investigations

FDB3384
DANIELLE DELUCY

Duration: 3 Hour

  Add To Cart
Recording
  

Effective Standard Operating Procedure (SOPs) Development for Regulatory Compliance

FDB1868
DANIELLE DELUCY

Duration: 75 Minutes

  Add To Cart
Recording
  

GMP Data Integrity – Implementation and Management

FDB1869
DANIELLE DELUCY

Duration: 75 Minutes

  Add To Cart
Recording
  

Investigating Deviations – Best Practices

FDB1860
DANIELLE DELUCY

Duration: 75 Minutes

  Add To Cart
Recording
  

Robust CAPA and Proper Root Cause Analysis

FDB2165
DANIELLE DELUCY

Duration: 75 Minutes

  Add To Cart
Recording
  

How to Properly Investigate OOS Results

FDB2166
DANIELLE DELUCY

Duration: 75 Minutes

  Add To Cart
Recording
  

How To Properly Manage a Regulatory Inspection

FDB2266
DANIELLE DELUCY

Duration: 75 Minutes

  Add To Cart
Recording
  

How to Conduct Successful Supplier Audits

FDB2164
DANIELLE DELUCY

Duration: 75 Minutes

  Add To Cart
Recording
  

Proper Root Cause Analysis

FDB2466
DANIELLE DELUCY

Duration: 75 Minutes

  Add To Cart
Recording
  

Sunshine Act Reporting – Clarification for Clinical Research

FDB3162
DANIELLE DELUCY

Duration: 75 Minutes

  Add To Cart
Recording
  

Achieving Compliance with Proper CAPA Systems

FDB2862
DANIELLE DELUCY

Duration: 60 Minutes

  Add To Cart
Recording
  

Capturing Justifications in Change Control, Risk Assessment, Validations, and Investigations

FDB2461
DANIELLE DELUCY

Duration: 75 Minutes

  Add To Cart
Recording
  

Successful Deviation Investigations

FDB2462
DANIELLE DELUCY

Duration: 60 Minutes

  Add To Cart
Recording
  

Guideline to Aseptic Technique and Clean Room Behavior

FDB2463
DANIELLE DELUCY

Duration: 75 Minutes

  Add To Cart
Recording
  

Laboratory Controls – Anticipate the Systems Based FDA Inspection

FDB2467
DANIELLE DELUCY

Duration: 75 Minutes

  Add To Cart
Recording
  

Process Validation LifeCycle

FDB2468
DANIELLE DELUCY

Duration: 75 Minutes

  Add To Cart
Recording
  

Conducting Successful Quality Audits

FDB2863
DANIELLE DELUCY

Duration: 75 Minutes

  Add To Cart
Recording
  

Biosafety and Blood borne Pathogen Safety in the Lab

FDB2861
DANIELLE DELUCY

Duration: 75 Minutes

  Add To Cart
Recording
  

Understanding Aseptic Technique and Cleanroom Behavior – Avoiding Human Error

FDB2865
DANIELLE DELUCY

Duration: 75 Minutes

  Add To Cart
Recording
  

Successful Change Control Management

FDB2868
DANIELLE DELUCY

Duration: 75 Minutes

  Add To Cart
Recording
  

3-Hour Virtual Seminar on Successful Deviation Investigations

FDB3081
DANIELLE DELUCY

Duration: 3 Hour

  Add To Cart
Recording
  

Critical Elements Of Quality Risk Management Relating to FDA Compliance

FDB2262
DANIELLE DELUCY

Duration: 75 Minutes

  Add To Cart
Recording
  

Effective Standard Operating Procedure (SOPs) Development

FDB3161
DANIELLE DELUCY

Duration: 75 Minutes

  Add To Cart
Recording
  

Step-By-Step Process For Successful Sterility Failure Investigations

FDB2465
DANIELLE DELUCY

Duration: 75 Minutes

  Add To Cart
Recording
  

3-Hour Virtual Seminar On Batch Record Review And Product Release

FDB3282
DANIELLE DELUCY

Duration: 3 Hour

  Add To Cart
Recording
  

3-Hour Virtual Seminar on Handling OOS Test Results and Completing Robust Investigations

FDB3384
DANIELLE DELUCY

Duration: 3 Hour