Bachem vs ST Pharm: CDMO Comparison

How does Bachem compare to ST Pharm for Oligo/ASO manufacturing?

Side-by-side comparison of Bachem and ST Pharm 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.

Bachem → 80.0
Bubendorf, CH
Signal Score
80/100
Quality (FDA + GMP)
95/100
FDA inspections
3
— NAI / VAI / OAI
0 / 3 / 0
FDA warning letters
0
EMA GMP certificates (active)
0
MHRA GMP certificates (compliant)
0
Clinical programs (matched)
0
Capacity
—
Modalities
Oligonucleotide
Seoul, South Korea
Signal Score
73/100
Quality (FDA + GMP)
89/100
FDA inspections
0
FDA warning letters
0
EMA GMP certificates (active)
0
MHRA GMP certificates (compliant)
0
Clinical programs (matched)
0
Capacity
—
Modalities
Oligonucleotide, mRNA

Key differences

  • Bachem has more FDA inspections on record (3 vs 0) — a deeper regulatory paper trail.
  • Both maintain clean enforcement records — no FDA OAI classifications or warning letters on file for either CDMO.

On a 13-modality CDMO landscape, both Bachem and ST Pharm qualify as Oligo/ASO manufacturers; Bachem carries the higher composite Signal Score for Oligo/ASO programs in this comparison.

What to evaluate for Oligo/ASO programs

Both Bachem and ST Pharm qualify as Oligo/ASO CDMOs. When choosing between them for Oligo/ASO programs, weigh these four dimensions specifically — each carries through to the side-by-side scorecard above.

Synthesis scale

Match synthesizer scale (mmol to mol) to your clinical and commercial demand, and confirm the CDMO can scale without shifting the impurity profile.

Chemistry & conjugation

Confirm experience with your backbone and modifications (phosphorothioate, 2'-MOE/F) and any conjugation (GalNAc, lipid) your molecule requires.

Purity & analytics

Full-length product, deletion/addition impurities, and residual metals drive release. Look for established orthogonal analytics.

Regulatory track record

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

See all Oligo/ASO CDMOs ranked by Signal Score →

Frequently asked: Bachem vs ST Pharm

How does Bachem compare to ST Pharm for Oligo/ASO manufacturing?

On CDMO Signal's composite Signal Score, Bachem is 80/100 and ST Pharm is 73/100; Bachem has 3 FDA inspections on record vs 0 for ST Pharm. Both are tracked in the CDMO Signal directory as Oligo/ASO CDMOs. The scorecard above breaks down every metric side by side — use it alongside each CDMO's individual profile for the full regulatory and clinical footprint.

Which has the stronger FDA inspection record, Bachem or ST Pharm?

Both Bachem and ST Pharm maintain clean enforcement records on file — no FDA warning letters and no OAI classifications. Bachem has 3 FDA inspections on record; ST Pharm has 0.

Which is better for Oligo/ASO manufacturing — Bachem or ST Pharm?

Both Bachem and ST Pharm are tagged as Oligo/ASO CDMOs in our directory, so both are credible options for Oligo/ASO programs. The most important differentiator for Oligo/ASO selection is typically synthesis scale: Match synthesizer scale (mmol to mol) to your clinical and commercial demand, and confirm the CDMO can scale without shifting the impurity profile. Review each CDMO's profile and inspection record before shortlisting.

What does the Signal Score gap mean in practice?

Bachem carries a Signal Score of 80/100 and ST Pharm carries 73/100 — a small lead for Bachem. 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 Bachem and ST Pharm 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.