We coordinate Ministry of Environment, Forest and Climate Change (MoEFCC) import approvals under Basel No. B1110. Updated for the October 15, 2024 Office Memorandum, we manage filings, compile dossiers, coordinate Chartered Engineer valuation reports, and ensure compliance for eligible medical systems.
Request Compliance ConsultationThe transboundary movement of pre-owned medical devices into India requires prior environmental clearances. We file Form-5 applications, present cases to the Technical Review Committee (TRC), and secure import clearances.
We keep all submittals updated with the latest Ministry guidelines to secure quick permissions.
A detailed technical dossier is needed for review by environmental experts. We compile system specifications, de-installation layout photos, age verification declarations, and service support letters.
Our dossiers demonstrate clinical efficacy, proving the imported systems are not intended for disposal as waste.
Customs rules require valuation audits from a certified Chartered Engineer. We coordinate physical on-site evaluations, calculate fair market value, certify residual life (>5 years), and generate the Chartered Engineer report.
Our valuation certificates align with customs parameters to prevent port delays.
Only specific high-value medical devices are permitted for import under the October 15, 2024 memorandum. We perform audits of system age, model numbers, software upgrades, and diagnostic scopes (such as CT, MRI, CBCT, and surgical robots).
Our audits confirm import eligibility before purchasing equipment.
Whether you need CDSCO Sugam portal onboarding, NABL ISO 17025 audits, radiation safety layouts, or MoEFCC import clearance approvals, our regulatory engineering specialists are ready to secure your approvals.
Request a call with our compliance leads. Receive complete document checklist verification in 15 minutes.