On-Site Emergency Plan (OEP)

“Lockene guided our Italian manufacturing facility through the entire BIS FMCS certification and DPIIT Furniture QCO audit seamlessly. Their regulatory team coordinated on-site audit preparations, lab test samples, and AIR representation in India with zero delays. Highly recommended for foreign manufacturers entering the Indian market.”

“Navigating Indian BIS standards for our polymer exports was daunting until we partnered with Lockene. From in-house testing equipment calibration to sample dispatch and NABL testing coordination, their technical team handled every detail flawlessly. We secured our CM/L license well ahead of schedule.”

“Lockene's regulatory auditors conducted a rigorous pre-audit at our Vietnam facility that uncovered critical documentation gaps before the official BIS inspection. Their hands-on support during the actual audit ensured a 100% first-attempt clearance without major non-conformities.”

“We engaged Lockene for BIS CRS registration and WPC ETA approvals across 18 new smart electronics SKUs. Their team managed the entire lab testing schedule across NABL accredited labs, portal submissions, and queries within just 3 weeks. Outstanding turnaround time and technical depth.”

“The expertise Lockene demonstrated during our luxury furniture compliance evaluation for India was top-notch. They mapped our production workflows directly against IS 17631 and IS 17632 standards, enabling smooth import clearance and customs compliance across our brand stores in India.”

“Managing EPR compliance for e-waste and plastic packaging across multiple state pollution control boards was complex. Lockene streamlined our entire PIBO registration on the centralized CPCB portal, calculated annual liabilities accurately, and fulfilled our recycling credit targets on time.”

“Lockene is our trusted partner for TEC MTCTE telecom approvals. Their senior consultants managed Essential Requirements (ER) test protocols, lab allocations, and security clearances for our 5G enterprise routers with utmost transparency and prompt communication throughout.”

“Lockene made our Class B and Class C medical device registration under CDSCO remarkably smooth. Their regulatory dossiers were thoroughly prepared with clinical evaluation summaries, resulting in rapid MD-15 import license approval without any audit queries.”