Rigorous standards, transparent processes, and unwavering commitment to regulatory excellence.
At Paarth Trade Solutions, compliance is not an afterthought — it's the foundation of everything we do. We understand that in pharmaceutical and industrial trade, regulatory adherence is critical to protecting public health, ensuring product integrity, and maintaining market access.
Our compliance framework spans the entire supply chain — from vendor qualification and manufacturing oversight to documentation, logistics, and final delivery. We work closely with regulatory experts and industry bodies to stay current with evolving requirements across all markets we serve.
Our team ensures compliance with major international regulatory standards.
We source exclusively from GMP-certified manufacturers and conduct regular audits to ensure production quality, hygiene, and consistency meet international pharmaceutical standards.
Our logistics and supply chain operations align with GDP guidelines, ensuring that pharmaceutical products maintain their quality and integrity throughout transportation and storage.
For products entering the European market, we ensure full REACH (Registration, Evaluation, Authorisation and Restriction of Chemicals) compliance, including safety data sheets and substance registrations.
For US-bound shipments, we coordinate FDA-related documentation, including Drug Master File (DMF) references, import alerts awareness, and facility registration verification.
Complete documentation handling — Certificates of Analysis (CoA), Certificates of Origin, Safety Data Sheets (SDS), commercial invoices, packing lists, and all required regulatory filings.
Pre-shipment inspections, batch testing verification, stability data review, and third-party laboratory analysis to ensure every shipment meets specifications.
A systematic approach to quality at every stage of the supply chain.
Comprehensive assessment of manufacturing facilities, certifications, production capacity, and quality management systems before onboarding any supplier.
Verification of all product documentation — CoA, SDS, DMF references, stability data, and regulatory certificates — before order placement.
Physical inspection and sampling at the manufacturing site, with third-party laboratory testing when required, prior to shipment dispatch.
Monitoring of shipping conditions, temperature control (where applicable), and documentation accuracy throughout the transportation process.
Final verification upon delivery, including documentation handover, condition assessment, and any required customs clearance support.
Ongoing support including batch traceability records, reorder management, and regulatory query handling for delivered products.
We work exclusively with certified partners and maintain documentation of all compliance credentials.
Our manufacturing partners hold ISO 9001, ISO 14001, and ISO 22000 certifications as applicable.
Pharmaceutical API suppliers comply with WHO-GMP manufacturing standards and undergo regular inspections.
Full batch traceability, change control documentation, and audit records maintained for every transaction.
For specific certifications or compliance documentation, please contact us.