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Medical Regulatory Affairs
LCH assists our pharmaceutical and healthcare principals with full-cycle medical affairs including product registration, pharmacovigilance, agency interactions, and more...
All Rounded Regulatory Services
Pharmaceuticals & Medical Device Equipment
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Assist both Pharmaceuticals and Medical Device Companies to register products in local markets
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Advisory for needed registration document
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Conduct testing at International Agencies if needed to comply with end user needs
Licenses
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Wholesale Dealer License
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Secondary Re-packaging of Pharmaceuticals (Licensed Pharmaceutical Manufacturer)
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Dealer license for Dangerous Drugs
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In-house pharmacist for documentation needs
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Team for pharmacovigilance and regulatory affairs
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Import un-registered pharmaceutical products on named patient / un-registered basis
Logistics
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Licensed and compliant temperature controlled warehouses - for dangerous drugs, cold chain storage, and medical products
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