Skip to main content Skip to search Skip to main navigation

FDA/CDER: Revised MAPP on cGMP Surveillance Inspections

The US FDA’s CDER revised the Manual of Policies and Procedures (MAPP) on managing surveillance inspections based on its Site Selection Model. The CDER staff uses this model to prioritise manufacturing sites for national and international routine quality-related cGMP surveillance inspections.

The 2023 version has been effective since 26 June 2023. It was amended in terms of quality system effectiveness and introduced a new risk factor related to

    "the compliance history of establishments in the country or region in which the establishment is located". This includes the history of violations related to products exported from such country or region that are subject to such regulation.

The risk factors of patient exposure (e.g., to the Coronavirus) and the inherent product risks introduced in 2018 are further clarified. Inherent product risks are associated with the product itself, e.g., dosage form, how the drug is administered, or the therapeutic class.

The following types of sites are excluded from prioritisation under this MAPP:

  • Human drug compounding outsourcing sites registered under section 503B of the FDCA
  • Medical gas sites, as a separate selection process manages these,
  • Excipients (however, these may be inspected when deemed necessary),
  • Drugs intended for use only in clinical trials (however, these may be inspected when deemed necessary)


CDER's Manual of Policies and Procedures (MAPPs) are federal directives and documentations of internal policies and procedures. MAPPs are required by law and made available to the public to make CDER a more transparent organization. By the way, the top five countries based on the number of sites in the catalog are the U.S., India, China, Germany, and Canada. The yearly CDER report on the state of pharmaceutical quality summarises and analyses the inspection findings. You may browse this interesting CDER report for the fiscal year 2022 right here.


Source:

CDER: MAPP 5014.1/Rev. 1 on CDER’s risk-based Site Selection Model

CDER: Report on the State of Pharmaceutical Quality 2022

Meet the GMP Compliance Adviser

The GMP Compliance Adviser is the world's largest knowledge portal for quality management in the pharma business. 

The demo access is non-binding and ends automatically.

Test it now for free

You may also be Interested in the Following Articles:

What are the quality requirements for pharmaceutical gases?

What are the quality requirements for pharmaceutical gases?

You can view the answer here:
Read more
EMA: Update on the Guideline “Stability Testing for Variations”

EMA: Update on the Guideline “Stability Testing for Variations”

The EMA has updated the guideline on stability testing for variations (Revision 3, applicable from 15 January 2026).
Read more
EU: Proposal for Simplification of Medical Device Rules

EU: Proposal for Simplification of Medical Device Rules

The European Commission has proposed targeted reforms to simplify the Medical Device Regulation (Regulation (EU) 2017/745, MDR) and the In Vitro Diagnostic Regulation (Regulation (EU) 2017/746, IVDR) and to address structural implementation challenges.
Read more
EU: Proposal for a European Biotech Act

EU: Proposal for a European Biotech Act

The European Commission has presented a proposal for a European Biotech Act aimed at strengthening Europe’s biotechnology potential and accelerating the translation of innovation from the laboratory to the market.

Read more
EMA: Concept Paper for the Revision of Annex 3 on Radiopharmaceuticals

EMA: Concept Paper for the Revision of Annex 3 on Radiopharmaceuticals

The EMA has published a concept paper outlining a future revision of Annex 3 (Manufacture of Radiopharmaceuticals) of the EU GMP Guidelines. The paper was developed in collaboration with PIC/S and adopted by the GMDP Inspectors Working Group (IWG) at its November meeting.

Read more
EMA: Q&A on QP Certification Without Physical EU Import

EMA: Q&A on QP Certification Without Physical EU Import

The EMA has published a new Q&A addressing QP certification for batches that are neither manufactured within the EU/EEA nor intended for the EU/EEA market, and that are not physically imported into the EU/EEA.

Read more
Previous
Next