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Sterling Pharma Solutions — Ringaskiddy
Ringaskiddy, Ireland · CDMO
Site facts
- Company
- Sterling Pharma Solutions
- Name(s) in FDA data
- Sterling Pharma Ringaskiddy Limited
- FEI number(s)
- 3002807776 (present in FDA Data Dashboard records for this name and city)
- Location (as in FDA data)
- Ringaskiddy, Ireland
- Records matched
- 6 FDA inspections
- Most recent FDA inspection in dataset
- 05 Apr 2022 — VAI
Capabilities (from the company's website)
- Lyophilization
…ro laboratory suite ‘Lasentec’ monitoring of crystallisation Centrifuge, filter dryer and lyophilisation equipment for isolation ‘Near Infra Red’ and online spectrometry monitoring for API…
- Small molecule
…ck here to view our full 360 tour. Related Services and Technologies API Manufacturing As small molecule complexity continues to rise, we deliver our customers the scientific and… Learn More Mil…
- API / drug substance (chemical)
…Cork, Ireland A dedicated API manufacturing facility with specialist expertise in peptide manufacturing and large scale…
- Highly potent (HPAPI)
…s Hydrogenation Water sensitive chemistry Corrosive chemistry Grignard reaction chemistry Highly potent APIs (HPAPIs) Solvent recovery Drug substance production Technology transfer State-of-the…
- Peptides & oligonucleotides
…Cork, Ireland A dedicated API manufacturing facility with specialist expertise in peptide manufacturing and large scale chromatography Located near a cluster of pharmaceutical inn…
- Spray drying & particle engineering
…s include: Peptide manufacturing Analytical development Chemistry development Milling and micronisation Large scale chromatography Low temperature reactions Hydrogenation Water sensitive c…
- Analytical testing
…ent through to commercialisation. Some of our key services include: Peptide manufacturing Analytical development Chemistry development Milling and micronisation Large scale chromatography Low temperatur…
Taken from the company's web page for this site. Source: https://www.sterlingpharmasolutions.com/facilities/cork-ireland/, checked 16 Oct 2026. Quoted text shows the wording each tag is based on.
Regulatory timeline
Newest first. Each entry links to the published source. Inspection classifications: NAI = no action indicated, VAI = voluntary action indicated, OAI = official action indicated (FDA definitions). Posted 483 citations are FDA's short summaries, not the full Form 483.
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05 Apr 2022FDA inspection FDA inspection classified VAI
Voluntary Action Indicated (VAI). Product type(s): Drugs. Project area(s): Drug Quality Assurance.
Source: FDA Data Dashboard – Inspections (FEI 3002807776, inspection ID 1271673)
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13 Sep 2019FDA inspection FDA inspection classified VAI
Voluntary Action Indicated (VAI). Product type(s): Drugs. Project area(s): Drug Quality Assurance.
Source: FDA Data Dashboard – Inspections (FEI 3002807776, inspection ID 1123878)
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03 Feb 2017FDA inspection FDA inspection classified NAI
No Action Indicated (NAI). Product type(s): Drugs. Project area(s): Drug Quality Assurance.
Source: FDA Data Dashboard – Inspections (FEI 3002807776, inspection ID 1004237)
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28 Mar 2014FDA inspection FDA inspection classified NAI
No Action Indicated (NAI). Product type(s): Drugs. Project area(s): Drug Quality Assurance.
Source: FDA Data Dashboard – Inspections (FEI 3002807776, inspection ID 881381)
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22 Sep 2010FDA inspection FDA inspection classified NAI
No Action Indicated (NAI). Product type(s): Drugs. Project area(s): Drug Quality Assurance.
Source: FDA Data Dashboard – Inspections (FEI 3002807776, inspection ID 694810)
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15 Oct 2008FDA inspection FDA inspection classified NAI
No Action Indicated (NAI). Product type(s): Drugs. Project area(s): Drug Quality Assurance.
Source: FDA Data Dashboard – Inspections (FEI 3002807776, inspection ID 548092)
This is a record of what regulators published, not a rating. Absence of a record here does not mean no record exists; see methodology for what we check and how records are matched.