Accuprec at CPHI Frankfurt 2025

Advancing Global Pharmaceutical Quality

Accuprec Research Labs Pvt. Ltd. is proud to participate in CPHI Frankfurt 2025, one of the world’s most prestigious exhibitions for the global pharmaceutical industry. The event brings together leading scientists, manufacturers, and innovators to showcase advancements shaping the future of healthcare.

Accuprec, our goal is to support the entire drug development lifecycle through high-quality, research-driven testing solutions that ensure safety, efficacy, and regulatory compliance. During CPHI Frankfurt 2025, we will highlight our specialized pharmaceutical testing services — from Extractables & Leachables (E&L) and Toxicological Risk Assessment (TRA) to Pre-Filled Syringe (PFS) Testing, Nitrosamine/NDSRI Analysis, IVRT & IVPT Studies, and Preclinical Research — designed to make drug development faster, safer, and globally accepted.

Representing Accuprec at CPHI Frankfurt 2025 will be:.

Dr. Rina Gokani

Director & CSO

Leading discussions on Toxicology, Extractable & Leachable Testing, and Regulatory Risk Assessment.

rina.gokani@accuprec.com
WhatsApp | LinkedIn

Mr. Mayur Kandoriya

Director & CMO

Driving strategic partnerships and client collaborations across global markets.

mayur.kandoriya@accuprec.com
WhatsApp | LinkedIn

Mr. Padmin Buch

Chairperson, Board of Advisors

Focusing on innovation strategy and regulatory quality systems.

padmin.buch@accuprec.com
+91 98258 84846 | LinkedIn

Mr. Dinesh Moga

General Manager (AD & QC)

Representing analytical and quality control excellence.

dinesh.moga@accuprec.com
+91 70433 78272 | LinkedIn

Mr. Deven Rasadiya

Manager (QC)

Supporting method validation and analytical services.

deven.rasadiya@accuprec.com
WhatsApp | LinkedIn


They will be available to discuss collaborations, outsourcing opportunities, and regulatory-driven testing partnerships.


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Our Specialized Focus Areas

Extractable & Leachable Testing & TRA

Comprehensive analysis of packaging interactions and toxicological evaluation.

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Toxicological / Preclinical Testing

GLP-compliant studies ensuring safe transition from lab to clinical stages.

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Nitrosamine & NDSRI Testing

Trace-level impurity detection using LC-MS/MS & GC-MS/MS for regulatory compliance.

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Pre-Filled Syringe (PFS) Testing – ISO 11040

Ensuring sterility, material compatibility, and ISO-compliant performance validation.

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Carrier Vesicles Characterization

Advanced particle, zeta potential, and stability profiling for liposomes & nanosomes.

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IVRT & IVPT Studies

In-vitro release and permeation testing for topical and transdermal formulations.

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