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.

Mr. Mayur Kandoriya
Director & CMO
Driving strategic partnerships and client collaborations across global markets.

Mr. Padmin Buch
Chairperson, Board of Advisors
Focusing on innovation strategy and regulatory quality systems.

Mr. Dinesh Moga
General Manager (AD & QC)
Representing analytical and quality control excellence.

Mr. Deven Rasadiya
Manager (QC)
Supporting method validation and analytical services.
They will be available to discuss collaborations, outsourcing opportunities, and regulatory-driven
testing partnerships.
Meet the Accuprec team at Hall 6.1 | Stall D96 | CPHI Frankfurt 2025 (28–30 October) | Book your meeting at info@accuprec.com
Schedule a Calendly Meeting
Our Specialized Focus Areas
Extractable & Leachable Testing & TRA
Comprehensive analysis of packaging interactions and toxicological evaluation.
Read MoreToxicological / Preclinical Testing
GLP-compliant studies ensuring safe transition from lab to clinical stages.
Read MoreNitrosamine & NDSRI Testing
Trace-level impurity detection using LC-MS/MS & GC-MS/MS for regulatory compliance.
Read MorePre-Filled Syringe (PFS) Testing – ISO 11040
Ensuring sterility, material compatibility, and ISO-compliant performance validation.
Read MoreCarrier Vesicles Characterization
Advanced particle, zeta potential, and stability profiling for liposomes & nanosomes.
Read MoreIVRT & IVPT Studies
In-vitro release and permeation testing for topical and transdermal formulations.
Read More