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Data & Facts

Data & Facts

Regulatory Performance

Regulatory Performance

Marketing Authorisation Procedures and Approvals
259
marketing authorisation procedures
were completed by the Paul-Ehrlich-Institut in 2021/22.

Subsequent Procedures After Marketing Authorisation
1,863
subsequent procedures
after marketing authorisation were assessed by the Paul-Ehrlich-Institut in 2021/22.

Paediatric Investigation Plans (PIPs) and Plasma Master Files (PMFs)
277
PIPs und PMFs
were assessed by the Paul-Ehrlich-Institut in 2021/22.

Product Testing
34,740
batches
were released by the Paul-Ehrlich-Institut in 2021/22.

Clinical Trials
2,292
clinical trials and field trials
were assessed by the Paul-Ehrlich-Institut in 2021/22.

Scientific Advice
582
instances of scientific advice
were provided by the Paul-Ehrlich-Institut in 2021/22.

Safety of Biomedicines (Pharmacovigilance)
1,191
pharmacovigilance reports and signals
were assessed by the Paul-Ehrlich-Institut in 2021/22.

Inspections
387
inspections
were conducted by the Paul-Ehrlich-Institut in 2021/22.