CC0 PUBLIC RECORD GRAPH Every score & timeline item links directly to its underlying U.S. FDA record (openFDA, ORA FOIA Reading Room, DECRS & OASIS).
Scoring Formula v2.0 & Legal Guardrails REST API v1
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GMPGraphv2.0
Global FDA Facility Graph & Co-Packer Intelligence
Facility Graph → Pharmaceuticals & Sterile/OTC Drugs → Cliantha Research Limited
INDEXABLE (PASSES DATA-SUFFICIENCY GATE)
Pharmaceuticals & Sterile/OTC Drugs FEI: 3017682080 🛡️ LEVEL 2 · VAI OBSERVATION FOLLOW-UP

Cliantha Research Limited

Registered Address: India (India)

For Brand Buyers: Cliantha Research Limited carries a BB (68/100) rating due to documented FDA activity centered on Personnel GMP Training, Gowning & Hygienic Practices. Before wiring a deposit, require written proof of CAPA closure and third-party ISO 17025 finished-batch release testing.
Connected FDA Sources (2): FDA ORA FOIA Electronic Reading Room, FDA OASIS Import Refusals · Resolved Name Aliases: Cliantha Research Limited
BB
68/100
Moderate (VAI)
7-Dim FDA Record Index v2.0
Ranks in the 25th percentile among Pharmaceuticals & Sterile/OTC Drugs facilities.
Based strictly on public U.S. FDA records as of 2026-11-03. See Formula v2.0
Dim 1 · Credit Grade
BB (68/100)
Recency-Weighted Index
Dim 2 · Inspection Shield
Level 2 / 4
Physically Inspected — Documented Form 483 Observations
Dim 4 · 'Elsa' Audit Odds
69%
MODERATE CYCLE WINDOW (6–12 Months)
Dim 5 · 180d WL Escalation
49%
483 → Warning Letter Risk
Dim 6 · Brand Contagion
10 Brands
~50 Downstream SKUs
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LAYER 4 · AI BUYER DUE-DILIGENCE INTERVIEW SCRIPT Tailored to FEI 3017682080's FDA Record

5 Questions to Ask Cliantha Research Limited Before Signing a Manufacturing Contract

Bring these exact questions to your discovery call with their QA Director or account rep before wiring a production deposit:

  1. Q1: On 2026-04-17, FDA cited 21 CFR 211.25(a) (Personnel GMP Training, Gowning & Hygienic Practices). Can your Quality Unit share the signed 15-day CAPA response and verification logs showing this gap is closed?
  2. Q2: On 2026-04-17, FDA cited 21 CFR 211.42(a) (Cleaning Validation, Sanitation Logs & Pest Control). Can your Quality Unit share the signed 15-day CAPA response and verification logs showing this gap is closed?
  3. Q3: Do you perform 100% FTIR/HPLC identity testing on incoming active ingredients in-house (21 CFR 111.75(a)(1)), or do you rely on vendor COAs?
  4. Q4: Will you sign our Quality Agreement Rider requiring 24-hour notification if an FDA investigator issues a Form 482 or Form 483 at FEI 3017682080?
  5. Q5: Can we review a redacted Master Manufacturing Record (MMR) and Batch Production Record (BPR) with dual-operator weight verification and yield reconciliation?

Cross-Database Regulatory & Inspection Timeline

Unified chronological history across FDA ORA Inspections, Form 483s, Warning Letters, Enforcement Recalls, and OASIS Import Refusals.

Form FDA 483 Issued · 2026-04-17
Open Full 483 Analysis & Dossier →

FDA Form 483 issued to Cliantha Research Limited (FEI 3017682080) on 2026-04-17 following an inspection of its producer of regulated products operations in India. The report documents 2 inspection observations centered on Personnel GMP Training, Gowning & Hygienic Practices, Cleaning Validation, Sanitation Logs & Pest Control.

  • 21 CFR 211.25(a) (Personnel GMP Training, Gowning & Hygienic Practices): Operators performing manufacturing or QA tasks without documented GMP/SOP training, or observed gowning/hygiene deviations in production rooms.
  • 21 CFR 211.42(a) (Cleaning Validation, Sanitation Logs & Pest Control): Incomplete equipment cleaning/sanitation logs, inadequate allergen or cross-contamination changeover validation, or gaps in facility pest exclusion. REPEAT OBSERVATION
OASIS Border Import Refusal (OASIS-2026-88115) · 2026-07-19
Port: Los Angeles / Long Beach, CA · Charge: FILTH / INSANITARY CONDITIONS (FD&C Act 402(a)(4))
The article appears to have been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with filth.

Manufacturer Right-of-Reply & Free Match Correction

GUARDRAIL PROTECTED

To ensure fairness and accuracy, facility owners may submit verified Form 483 closeout evidence, CAPA completion statements, or entity-resolution corrections free of charge. Sponsorship never alters an FDA Record Index score.

Dimension 3 · FDA 6-System Model

6-Subsystem cGMP Radar Breakdown

Sub-scores mapped across FDA's six core inspection subsystems.

Quality System (CAPA & OOS) 71/100
Materials & Incoming Identity 69/100
Production & Batch Records 70/100
Facilities, Sanitation & Pest 58/100
Laboratory & Stability Controls 69/100
Packaging & Allergen Labeling 73/100
Layer 6 · Clean-Record Sourcing Alternatives

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Score Provenance Receipts

Every point in this facility's FDA Record Index (68/100) is backed by a linked government record (36-month half-life decay).

Event Date Weight Receipt
Inspection Outcome (VAI) 2026-04-17 -8.8 pts INSP-483-3017682080-20260417 ↗
Form 483 (2 observations, 1 repeat) 2026-04-17 -7.9 pts 483-3017682080-20260417 ↗
Import Refusal (FILTH / INSANITARY CONDITIONS) 2026-07-19 -7.5 pts OASIS-2026-88115 ↗