---
name: Raptim Research
slug: raptimresearch
site: cro
website_domain: raptimresearch.com
summary: Bioequivalence and bioavailability specialist with 32+ USFDA inspections cleared, running healthy-subject BA/BE and PK/PD studies, IVRT/IVPT in-vitro release and permeability testing, and Phase I to IV clinical trials. Headquartered in Navi Mumbai, India.
tagline: Global CRO for BA/BE, in-vitro release testing, and early- to late-phase clinical research
founded_year: 
employee_count_band: 
employee_count_label: 
parent_name: 
parent_slug: 
hq_country: IN
tier2_domain_verified: false
updated_at: 2026-11-02T07:02:53.731Z
services_count: 8
modalities_count: 1
indications_count: 0
locations_count: 3
review_signal_gate: closed
generated_by: BioBM Editorial AI
---

# Raptim Research

Global CRO for BA/BE, in-vitro release testing, and early- to late-phase clinical research

Listed on cro.directory.

## Summary

Bioequivalence and bioavailability specialist with 32+ USFDA inspections cleared, running healthy-subject BA/BE and PK/PD studies, IVRT/IVPT in-vitro release and permeability testing, and Phase I to IV clinical trials. Headquartered in Navi Mumbai, India.

## At a glance

- HQ country: IN

## Services

- Clinical Trial Services
- Phase I Clinical Trials
- Phase II Clinical Trials
- Phase III Clinical Trials
- Phase IV / Post-Marketing
- Bioanalysis
- In Vivo PK / PD Studies
- Quality Control Testing

## Modalities

- Biologics (Other)

## Locations

- Navi Mumbai, Navi Mumbai, Maharashtra, India
- Gandhinagar facility, Gandhinagar, Gujarat, India
- Mumbai Phase I facility, Mumbai, Maharashtra, India

## Long description

Raptim Research is a contract research organization offering regulatory-compliant services across clinical trials, BA/BE, and bioanalytical studies for Biopharma, medical device, and consumer healthcare clients.

## Services

- **BA/BE:** Healthy subject bioequivalence and bioavailability studies, pharmacokinetics (PK), pharmacodynamics (PD), and patient-based PK/PD and clinical endpoint (CE) studies.
- **In-vitro studies:** In-vitro release rate testing (IVRT) and in-vitro permeability testing (IVPT), in-vitro binding studies, and BCS biowaiver studies.
- **Special studies:** In vivo tape stripping, in vivo dermal microdialysis, skin blanching, skin irritation and sensitization testing, and glucose clamp studies.
- **Clinical trials:** Early phase clinical trials, patient-based PK/PD/CE studies, Phase II-III trials, and Phase IV and post-marketing studies.
- **Bioanalytical lab:** Bioanalytical method development and validation, with over 600 validated methods cited on the site.

## Regulatory and infrastructure

- Cleared 32+ USFDA inspections along with other audits by major regulatory authorities, according to the site.
- Milestones listed include a UK MHRA inspection, a WHO inspection, and GCC approval.
- Clinical capacity is stated as 390 beds in total, including a 12-bed Phase I facility in Mumbai and 38 beds approved for BA/BE studies.
- Quality assurance and quality control work covers IVRT/IVPT, NG tube, inhalers, and BCS biowaivers.

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_Profile last updated: 2026-11-02T07:02:53.731Z. Profile facts may include AI-assisted enrichment._

Auto-generated by BioBM Editorial AI for machine-readable profile access.