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QUALITY RISK MANAGEMENT (QRM)

Original price was: ₹600.00.Current price is: ₹500.00.

PREMADE DOCUMENTS IN MICROSOFT SOFT WORD COPY

SOP ON QUALITY RISK MANAGEMENT (QRM) WITH ATTACHMENTS

  • Attachment-I: Quality Risk Management Process Flow Diagram
  • Attachment-II: Quality Risk Management- Material Management (QRM-MM)
  • Attachment-III: Quality Risk Management- Facility, Equipment & Utilities (QRM-FEU
  • Attachment-IV: Quality Risk Management- Production System-Manufacturing, Packaging and Labeling (QRM-PS).
  • Attachment-V: Quality Risk Management- Laboratories Control System (QRM-LCS).
  • Attachment-VI: Quality Risk Management- Method and Procedure (QRM-MP)
  • Attachment-VII: Risk management log
  • Attachment-VIII: Risk Assessment Template
  • Attachment-IX: Quality Risk Management Tools Selection decision tree
  • Attachment-X: Risk Assessment, Mitigation Plan & Summary Report (Quantitative Approach)
  • Attachment-XI: Risk Assessment, Mitigation Plan & Summary Report (Qualitative Approach)
  • Attachment-XII: Risk Assessment Fault Tree Analysis (FTA)
  • Attachment-XIII: Risk Assessment Hazard Operability Analysis (HAZOP)
  • Attachment-XIV: Risk Assessment Preliminary Hazard Analysis (PHA)
  • Attachment-XV: Risk Assessment Hazard Analysis and Critical Control Points (HACCP)
  • Attachment-XVI: Risk Assessment Review And Status
  • Attachment-XVII: Year-Wise List of Identified Major and Critical Risk
  • Attachment-XVIII: Template for Qualification Risk Assessment Protocol

Creating SOPs in a pharmaceutical project requires a significant amount of time, effort, and human resources. Months are dedicated to the creation and review of documents, yet they often remain incomplete. Our pre-made documents offer a solution by saves both time and manpower. They enable the timely initiation of production, which is advantageous for your company. In the business world, time is equivalent to money.

One-click & Download and create A SOP without any Extra Efforts

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PREMADE DOCUMENTS IN MICROSOFT SOFT WORD COPY

SOP ON QUALITY RISK MANAGEMENT (QRM) WITH ATTACHMENTS

  • Attachment-I: Quality Risk Management Process Flow Diagram
  • Attachment-II: Quality Risk Management- Material Management (QRM-MM)
  • Attachment-III: Quality Risk Management- Facility, Equipment & Utilities (QRM-FEU
  • Attachment-IV: Quality Risk Management- Production System-Manufacturing, Packaging and Labeling (QRM-PS).
  • Attachment-V: Quality Risk Management- Laboratories Control System (QRM-LCS).
  • Attachment-VI: Quality Risk Management- Method and Procedure (QRM-MP)
  • Attachment-VII: Risk management log
  • Attachment-VIII: Risk Assessment Template
  • Attachment-IX: Quality Risk Management Tools Selection decision tree
  • Attachment-X: Risk Assessment, Mitigation Plan & Summary Report (Quantitative Approach)
  • Attachment-XI: Risk Assessment, Mitigation Plan & Summary Report (Qualitative Approach)
  • Attachment-XII: Risk Assessment Fault Tree Analysis (FTA)
  • Attachment-XIII: Risk Assessment Hazard Operability Analysis (HAZOP)
  • Attachment-XIV: Risk Assessment Preliminary Hazard Analysis (PHA)
  • Attachment-XV: Risk Assessment Hazard Analysis and Critical Control Points (HACCP)
  • Attachment-XVI: Risk Assessment Review And Status
  • Attachment-XVII: Year-Wise List of Identified Major and Critical Risk
  • Attachment-XVIII: Template for Qualification Risk Assessment Protocol

Creating SOPs in a pharmaceutical project requires a significant amount of time, effort, and human resources. Months are dedicated to the creation and review of documents, yet they often remain incomplete. Our pre-made documents offer a solution by saves both time and manpower. They enable the timely initiation of production, which is advantageous for your company. In the business world, time is equivalent to money.

One-click & Download and create A SOP without any Extra Efforts