From new drugs and generics to biopharmaceuticals and advanced biopharmaceuticals,
Meditip has secured over 1,200 regulatory approvals across a wide range of therapeutic areas.
Over 1,200 pharmaceutical regulatory approvals secured
Drawing on hands-on experience accumulated across diverse therapeutic areas and product categories, we expertly handle everything from approval strategy development to MFDS response and global registration.
From medical supplies, medical equipment, IVD, and diagnostic devices to orthopedic products, Meditip has secured over 1,300 regulatory approvals across a wide range of product categories.
Over 1,300 medical device regulatory approvals secured
From manufacturing, import, and renewal to technical document review and approval strategies for IVD and each product category, we provide optimal solutions based on extensive medical device regulatory experience.
Across diverse functional areas such as immunity, cognition, body fat, blood glucose, skin, and gut health, Meditip has completed over 100 individually approved human application trials and regulatory approvals.
Over 100 individually approved human application trials and regulatory approvals across diverse functional areas
From functional ingredient development to human application trials, individual approval registration, and MFDS response, we provide optimal strategies based on expertise across the entire health functional food lifecycle.
Centered on Orthopedics, Cardiovascular, Dermatology, and Oncology,
Meditip has accumulated clinical operations and development experience across a wide range of therapeutic areas.
Extensive clinical trial experience across diverse therapeutic areas, with over 400 studies conducted
Backed by professionals with extensive experience in multinational and domestic pharmaceutical companies and CRO projects, we provide high-quality clinical trial services that comply with KGCP and ICH-GCP Guidelines.
