Clear records for confident procurement.
Company registration references and product-specific documents help your team review the proposed supply and implementation scope.
Registration details, in one place.
Import / Export Certificate
Drug Licence Certificate
MD-42 Registration
Match each document to the equipment.
The following are document categories that may be relevant to your project. Applicability and availability are reviewed for the selected manufacturer, model and supply scope.
CE
CE marking and relevant conformity documentation for the specific product, where applicable.
Review by product / scopeUSFDA
Applicable US FDA clearance, approval or other device-specific records. Registration and listing alone do not establish approval.
Review by product / scopeEU
Relevant European Union product conformity documents, where applicable to the selected equipment.
Review by product / scopeBIS
Applicable Bureau of Indian Standards licence or product certification details, where required.
Review by product / scopeCDSCO
Applicable Central Drugs Standard Control Organisation licences or regulatory documents for the product and supply route.
Review by product / scopeISO Certificate
Relevant organisation or manufacturer certificate, including the standard, certified scope, issuing body and validity.
Review by product / scopeThese categories are not a claim that every Medisky product—or Medisky itself—holds every listed certification. Company registrations and product conformity documents serve different purposes.
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