ACCUPREC
ACCURACY + PRECISION
1000+
2012
- 9 International Accreditations including ISO/IEC 17025:2017, ISO 9001:2015, OECD-GLP, AAALAC, DUNS, USFDA, EMA, ASCA-A2LA, Canada Health as well as
- 11 National Accreditations including FDCA, FDCA-GLP, CCSEA, AYUSH, DSIR, CDSCO-MD40, FDCA-Cosmetic, CIBRC, RCGM-DBT, BIS, CDSCO-CT07C
A Leading Contract Research Organization
Detect trace carcinogenic impurities with validated methods for global regulatory compliance readiness.
Identify chemical leachables from packaging and devices with full toxicological risk assessment support.
Comprehensive in-vitro, in-vivo, and bioanalytical testing aligned with global regulatory standards.
Evaluate drug release and skin permeation to ensure bioequivalence and formulation performance.
Driven by Science. Guided by Global Compliance.
Scientific Integrity
We conduct every study with uncompromising scientific rigor, data accuracy, and ethical responsibility.
Regulatory Excellence
Our work aligns with global regulatory standards including USFDA, EU MDR, OECD, and NABL requirements.
Quality & Precision
We ensure validated methods, reliable results, and consistent quality across all testing and research activities.
Client Partnership
We work as an extension of our clients’ teams, supporting them from development through regulatory approval.
You’ll Know What
Driving the vision and operational precision of Accuprec's global services.
Expert in biocompatibility and toxicological risk assessment for global compliance.
Leading complex Nitrosamine studies and advanced analytical research.
Architecting global partnerships and international market strategies.
Accredited Contract Research Organization in India
We support pharmaceutical, medical device, and regulated industries with reliable testing, research, and regulatory services – delivered with scientific rigor and transparency at every stage.
National Accreditations
International Accreditations
Hear Directly
From Accuprec Experts
Frequently Asked Questions
Common questions about our testing, research, and regulatory services
What services does Accuprec provide as a Global CRO partner in India?
Accuprec provides contract research and testing services across pharmaceuticals, medical devices, cosmetics, food, nutraceuticals, and regulated products, including analytical testing, microbiology, stability, clinical support, and regulatory documentation.
Which regulatory standards do you work with?
We operate in alignment with global regulatory frameworks such as USFDA, EU MDR, OECD, NABL, and applicable ISO standards, depending on the scope and market requirements of the project.
Do you support products intended for international markets?
Yes. We support clients targeting global markets by ensuring testing and documentation meet international regulatory expectations for submissions in the US, Europe, and other regulated regions.
Can you assist with regulatory documentation and submissions?
We provide regulatory support including dossier preparation, technical documentation, validation reports, and compliance guidance to support regulatory submissions and audits.
