Integrated Solutions
Meditip provides the core services required across the entire healthcare product development process,
from development and regulatory approval to clinical trials and global market entry.
Development & Regulatory Approval Services
We handle full-cycle regulatory approval for pharmaceuticals, medical devices, and health functional foods, from establishing development strategy to regulatory approval and insurance listing.
Learn MoreCDMO Operations
From investigational medicinal product manufacturing to QMS-based quality management and GMP technology transfer, we support the optimization of overall CDMO operations and the establishment of a stable development environment.
Learn MoreNon-clinical Services
From establishing non-clinical strategy to domestic and overseas CRO coordination and efficacy evaluation, we provide non-clinical services across the entire new-substance development lifecycle.
Learn MoreClinical Services
From establishing clinical strategy to Clinical Operations, Data Management, and QA/QC, we provide specialized services for high-quality clinical trial execution.
Learn MoreICC
For overseas companies seeking to enter the Korean market without a local corporation, we take full responsibility for the entire process, from legal representation and regulatory approval to product maintenance and supply management.
Learn MoreGlobal Market Entry
From establishing country-specific regulatory strategy to overseas certification and local registration, we systematically advance the entire global market entry process.
Learn MoreCOMPANY
Meditip is a One-Stop consulting partner that increases our clients' likelihood of success, from early-stage development strategy to approval, clinical trials, and commercialization.
Discovery
Efficacy & Toxicity Testing / Non-clinical Strategy
Development
IND / IDE / Clinical / Human Application Trials
20+ Years of Know-How / 2,200+ Clinical Trials
Commercialization
NDA / BLA / Reimbursement / Drug Pricing
Late Phase Study
US FDA / Europe EMA / China NMPA / Japan PMDA
EXPERIENCES
Backed by extensive regulatory approval and clinical experience, we have built proven expertise and tangible success stories.
R&D SUPPORT
From product commercialization and CDMO to government R&D projects, we continue to provide strategic R&D support for development success and business expansion.
Product Commercialization Support
We provide strategic support so that R&D achievements can lead to actual market entry and commercialization.
Learn MoreCDMO Operations Consulting
Through QMS-based process optimization and GMP technology transfer, we enhance the efficiency of investigational medicinal product manufacturing operations.
Learn MoreGovernment R&D Project Participation
From project planning, institution matching, and milestone management to annual reporting, we support the entire process of executing government R&D projects.
Learn MoreGLOBAL FAMILY NETWORK
Based on our global Family brands and specialized collaboration network, we connect an expanded development infrastructure spanning from non-clinical work to global market entry.
INSIGHT
Press Coverage
Newsletter
[No. 872] MFDS Conducts Its First International Joint Review of Pharmaceuticals with Overseas Regulatory Authorities, Including Europe
[No. 871] MFDS Selects 'Bio Challenger' Program to Support the Commercialization of Innovative Advanced Biopharmaceuticals
[No. 870] Notice of Administrative Pre-Announcement on the Partial Amendment to the Regulations on Pharmaceutical Approval, Notification, and Review
SERVICE ACCESS
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