Hosting Regulatory Inspections - GMP SOP
The aim of the Hosting Regulatory Inspections program is, firstly, to ensure that a well defined and professional inspection process during FDA or any other regulatory Inspection in connection with pharmaceutical development, manufacturing, testing of materials products or medical devices at your site.
This is a must and also crucial prerequisite for a successful outcome of the authority inspection. This Standard Operating Procedure (SOP) provides all information that should be considered during a regulatory inspection. The SOP covers the whole inspection, starting with the arrival of the investigators/inspectors on site, following the inspection activities and ends with the final close out meeting of the inspection.
The SOP gives also an overview about the organization of the inspection team and the roles and responsibilities of the involved site personnel like Inspection Coordinator, Scribe, Runner and Subject Matter Expert. This 18-page SOP, which includes four attachments – is ready to use and only needs small site specific adoption.
Table of Content
1. Regulatory Basis, Reference Documents
4. Responsibilities and Accountabilities
4.1. Responsibility of Receptionist or designee
4.2. Responsibility of all Employees
4.3. Responsibility of Quality Assurance Manager or designee
4.4. Responsibility of Quality Assurance Personnel or designee
4.5. Responsibility of Regulatory Affairs Department
5.1. General Considerations
5.2. Arrival of the Inspector/Investigator
5.3. Inspection Opening Meeting
5.4. During the Inspection
5.4.2 Daily Debriefing Meetings
5.4.3 Daily Internal Meetings
5.4.4 Inspection Closing Meeting
5.4.5 Post-Inspection Meeting
5.5. Observations Requiring Corrective Actions
5.6. Preparation of Formal Responses
5.7. Compiling the Inspection File
Attachment 1: Inspection Roles
Attachment 2: Regulatory Inspection Summary
Attachment 3: Opening and Closing Meeting Attendance
Attachment 4: Submission of Samples to Regulatory Agencies
|SKU||Hosting Regulatory Inspections - GMP SOP|
What you will get:
Delivery item: Word Document
You will be able to enter your data into the Word document.
Please note: We do not deliver hard copies.
- Computer system validation and maintenance checklist - GMP ChecklistRegular Price $220.00 Today $197.00+ 19% german VAT when applicable
- PAI Protocol For Drug Products - GMP ChecklistRegular Price $240.00 Today $209.00+ 19% german VAT when applicable
- 21-CFR 820 Quality systems GMP ChecklistRegular Price $260.00 Today $219.00+ 19% german VAT when applicable
- Self-Inspection Program - GMP SOPRegular Price $100.00 Today $79.00+ 19% german VAT when applicable