Catalent vs Richter BioLogics: CDMO Comparison

Side-by-side comparison of Catalent and Richter BioLogics on independent FDA inspections, EMA and MHRA GMP certificates, clinical-program activity, and CDMO Signal Score. Data sourced from FDA, EMA EudraGMDP, MHRA GMDP, and ClinicalTrials.gov.

Somerset, NJ (now operating under Novo Holdings, HQ effectively Bagsværd, Denmark)
Signal Score
76/100
Quality (FDA + GMP)
79/100
FDA inspections
10
— NAI / VAI / OAI
3 / 6 / 1
FDA warning letters
2
EMA GMP certificates (active)
16
MHRA GMP certificates (compliant)
16
Clinical programs (matched)
0
Capacity
Modalities
Monoclonal Antibody, Recombinant Protein, ADC, AAV, mRNA, Plasmid DNA, Fill-Finish
Hamburg, Germany
Signal Score
83/100
Quality (FDA + GMP)
100/100
FDA inspections
0
FDA warning letters
0
EMA GMP certificates (active)
9
MHRA GMP certificates (compliant)
0
Clinical programs (matched)
0
Capacity
Modalities
Plasmid DNA, Recombinant Proteins, VHH/Nanobodies, Bacterial Vaccines, Biologics

Key differences

  • Catalent has more FDA inspections on record (10 vs 0) — a deeper regulatory paper trail.
  • Catalent has 2 FDA warning letters on record; Richter BioLogics has none.
  • Catalent maintains 16 MHRA / UK GMP certificates; Richter BioLogics does not.

On a 13-modality CDMO landscape, both Catalent and Richter BioLogics qualify as Plasmid DNA manufacturers; Richter BioLogics carries the higher composite Signal Score for Plasmid DNA programs in this comparison.

What to evaluate for Plasmid DNA programs

Both Catalent and Richter BioLogics qualify as Plasmid DNA CDMOs. When choosing between them for Plasmid DNA programs, weigh these four dimensions specifically — each carries through to the side-by-side scorecard above.

GMP grade & purity

Confirm GMP (vs research/HQ) grade, supercoiled percentage, and residual host-cell DNA/RNA and endotoxin specs — these gate downstream vector and mRNA quality.

Fermentation scale & yield

Match fermentation scale and yield to your vector or mRNA demand. Ask about high-yield strains and whether scale-up is validated.

Lead time

Plasmid is a common critical-path bottleneck. Evaluate realistic queue and turnaround against your program timeline.

Regulatory track record

Cross-check FDA 483 history and EMA/MHRA GMP coverage — both shown above and on each profile.

See all Plasmid DNA CDMOs ranked by Signal Score →

Frequently asked: Catalent vs Richter BioLogics

Which has the stronger FDA inspection record, Catalent or Richter BioLogics?

Catalent has 10 FDA inspections on record (NAI 3 / VAI 6 / OAI 1) and 2 warning letters. Richter BioLogics has 0 FDA inspections on record (NAI 0 / VAI 0 / OAI 0) and 0 warning letters.

How do Catalent and Richter BioLogics compare on European GMP coverage?

Catalent holds 16 active EMA GMP certificates and 16 MHRA / UK certificates. Richter BioLogics holds 9 active EMA GMP certificates and 0 MHRA / UK certificates. Use these counts as a proxy for the breadth of each CDMO's European regulatory footprint.

Which is better for Plasmid DNA manufacturing — Catalent or Richter BioLogics?

Both Catalent and Richter BioLogics are tagged as Plasmid DNA CDMOs in our directory, so both are credible options for Plasmid DNA programs. The most important differentiator for Plasmid DNA selection is typically gmp grade & purity: Confirm GMP (vs research/HQ) grade, supercoiled percentage, and residual host-cell DNA/RNA and endotoxin specs — these gate downstream vector and mRNA quality. Review each CDMO's profile and inspection record before shortlisting.

What does the Signal Score gap mean in practice?

Catalent carries a Signal Score of 76/100 and Richter BioLogics carries 83/100 — a small lead for Richter BioLogics. The Signal Score combines quality (FDA inspections + EMA/MHRA GMP), operational performance, financial stability, and capacity intelligence. CDMOs cannot pay to influence their score.

Evaluating Catalent and Richter BioLogics for a program?

Use the free AI matchmaker to weigh both against your specific requirements — capacity, modality, regulatory record, geography — and surface other qualified options.

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Sourced from FDA, EMA EudraGMDP, MHRA GMDP, and ClinicalTrials.gov.