Meet ACCUPREC at CPHI Americas 2026

CPHI Americas 2026

Advancing Pharmaceutical & Medical Device Testing Through Scientific Precision

ACCUPREC Research Labs Pvt. Ltd. is proud to participate in the prestigious CPHI Americas 2026 — one of the leading global events for pharmaceutical innovation, networking, and strategic collaboration. Join us at the Pennsylvania Convention Center and explore how ACCUPREC is helping pharmaceutical and medical device companies achieve excellence through advanced analytical, toxicological, and characterization solutions.

Booth 1645
02 – 04 June 2026
Pennsylvania Convention Center
Event
CPHI Americas 2026
Date
02 – 04 June 2026
Venue
Pennsylvania Convention Center
Booth Number
1645

Our scientific experts will be available to discuss regulatory-focused testing strategies, customized research solutions, and comprehensive support for product development, quality assurance, and compliance.

Our Certifications & Accreditations
ISO 17025 Certified Laboratory
OECD-GLP Certified Facility
ASCA-A2LA Accredited Laboratory
AAALAC Accredited Facility
EMA Approved Laboratory
USFDA Approved Laboratory
Health Canada Compliant Facility
D-U-N-S® Registered Organization

These certifications reflect our commitment to international quality standards, scientific reliability, and regulatory excellence.

Meet Our Directors
Dr. Rina Gokani
CSO
Dr. Rina Gokani
Director & Chief Scientific Officer

Leading scientific operations with extensive expertise in pharmaceutical and medical device research, quality systems, and compliance-driven testing solutions.

+91 90996 16769
Dr. Manish Rachchh
CEO
Dr. Manish Rachchh
Director & Chief Executive Officer

Driving strategic growth and innovation while ensuring global quality standards across laboratory operations and customer solutions.

+91 90999 81023
Mr. Mayur Kandoriya
CMO
Mr. Mayur Kandoriya
Director & Chief Marketing Officer

Managing global business development, client engagement, and international partnerships across pharmaceutical and medical device sectors.

+91 99099 19545
Comprehensive Pharmaceutical & Medical Device Testing Solutions

At ACCUPREC, we combine scientific expertise, advanced instrumentation, and regulatory understanding to deliver reliable and globally compliant testing solutions for pharmaceutical, biopharmaceutical, and medical device industries.

01
Nitrosamine & NDSRI Testing

Comprehensive identification, detection, and quantification of Nitrosamines and NDSRIs using highly sensitive and regulatory-compliant analytical methodologies aligned with global expectations.

Risk Assessment Trace-level Analysis Method Validation Reg Reporting
02
Extractable & Leachable (E&L) Testing & Toxicological Risk Assessment (TRA)

End-to-end E&L studies for pharmaceutical packaging systems, medical devices, and drug delivery components, supported by scientifically driven toxicological risk assessments.

Extraction Studies Leachable Profiling Tox Evaluation Reg Docs
03
Toxicological & Preclinical Testing

Integrated toxicology and preclinical testing solutions supporting drug development programs with reliable safety evaluation, biological assessment, and regulatory compliance studies.

Safety Profiling Tox Evaluations Reg Support Preclinical Research
04
Iron Carbohydrate Complex Characterization

Advanced physicochemical characterization services for iron carbohydrate complexes through detailed structural, compositional, and comparative analytical evaluations.

Structural Analysis Particle Evaluation Spectroscopy Chromatography
05
Carrier Vesicles Based Particle Characterization

Comprehensive characterization solutions for liposomes, nanosomes, and other carrier vesicle systems using advanced analytical instrumentation and scientific methodologies.

Particle Size Surface Charge Morphology Stability
06
IVRT & IVPT Studies

Scientifically robust In-Vitro Release and Permeation Testing studies supporting topical and transdermal product development, equivalence studies, and regulatory submissions.

Topical Formulations Generic Comparison Performance Eval Reg Submission
07
Method Development & Validation (MDV)

Customized analytical method development, optimization, transfer, and validation services in compliance with international regulatory guidelines including ICH.

Method Dev Optimization Transfer Studies ICH Validation
08
Pre-Filled Syringe (PFS) Testing – ISO 11040

Comprehensive Pre-Filled Syringe testing solutions in accordance with ISO 11040 standards ensuring product integrity, functionality, compatibility, and patient safety.

Functional Testing Container Closure Compatibility Reg Compliance
09
Formulation & Development Services

Comprehensive formulation and development solutions designed to support pharmaceutical companies from early-stage development to commercial readiness.

Pre-formulation QbD Development Scale-Up Tech Transfer
Why Connect with ACCUPREC at CPHI Americas 2026?
Globally trusted pharmaceutical & medical device testing partner
Expertise in complex analytical and characterization studies
Strong regulatory and scientific approach
Advanced instrumentation & experienced scientific team
Customized solutions for innovators and generic manufacturers
End-to-end support from development to compliance
Let’s Connect

Meet Us at Booth 1645

Meet the ACCUPREC scientific team at Booth 1645 to discuss your pharmaceutical, biopharmaceutical, and medical device testing requirements. Whether you are looking for advanced analytical support, toxicological evaluations, characterization studies, or regulatory-compliant testing solutions — ACCUPREC is ready to support your development journey.

Schedule a Meeting
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