Your partner in global healthcare regulatory approval and clinical development
Meditip Co., Ltd. is a specialized healthcare regulatory approval and clinical development consulting company that leverages extensive information, knowledge, and experience to help clients' products enter domestic and global medical markets quickly and reliably.
We provide full-cycle consulting across the pharmaceuticals, medical devices, and health functional food fields, covering regulatory approval, insurance, clinical trials, post-market management, market research, and commercialization strategy.
Specialized Collaboration Network
We provide a stable project execution framework built on an organic collaboration structure with specialized organizations in each field, including non-clinical, clinical, and early human application trials.
Global Regulatory Approval Network and Market Entry
Through collaboration with global partners including Tigermed, we support overseas regulatory approvals and market entry strategies more quickly and effectively.
-
FDA (U.S.) / EMA (Europe) NMPA (China) / PMDA (Japan) support
-
Collaboration with global partners
-
Market research and distribution partner sourcing
-
Product commercialization strategy
One-Stop Total Solution Consulting Services from A to Z
From the R&D stage through non-clinical, clinical, regulatory approval, commercialization, and post-market studies, we provide integrated consulting services spanning the entire product development cycle through organic collaboration with specialized group companies in each field.
Discovery
Efficacy & Toxicity Studies / Non-clinical Strategy
Development
IND / IDE / Clinical Trials / Human Application Trials
20+ Years of Expertise / 2,200+ Clinical Trials Experience
Commercialization
NDA / BLA / Insurance / Drug Pricing
Late Phase Study
U.S. FDA / Europe EMA / China NMPA / Japan PMDA