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Pristine New Leader — Committed to Becoming a Trusted Global Clinical Research Solutions Provider
New Breakthrough! GCP ClinPlus Assists Conber Pharma in Securing Approval for Novel Dry Eye Drug
China's First! GCP ClinPlus Empowers Gensci's Groundbreaking Gout Drug to Market Success
One major topic at ASGCT 2026 was the growing interest in using China's IIT pathway to accelerate early clinical development for CGT programs
Long Jiang – CEO, GCP ClinPlus
Deep in Ophthalmology, Partnering with Santen｜GCP ClinPlus Empowers Clinical R&D with Data Science & AI
GCP ClinPlus and ProBio Partner to Accelerate Clinical Trials in China
Exhibitions & Events
Lancet-Validated Milestone: GCP ClinPlus' Biostatistics Team Elevates China's Influenza Drug Research onto the World Stage
National Respiratory Center Salutes GCP ClinPlus with Prestigious Research Award
Empowering 210+ Marketed Innovations: GCP ClinPlus Honored as ''Best Enabling Service Partner''
Insights
Regulatory Intelligence
Oligonucleotide therapeutics are moving beyond rare diseases and into the mainstream of chronic, high-burden disease innovation
Global Perspective | Rare Disease Drug Development: Regulatory Incentives and Market Opportunities
Compliance Outlook | China's IITs Under the New Regulatory Framework: Toward Standardized, Traceable, and Translation-Ready Research
From “Treatment” to“Cure”: The Disruptive Evolution of the CGT Clinical Evaluation System
China Accelerates Clinical Trials Approval to Just 30 Days
2026 H1 Trends in Oncology Clinical Trials
Cases & Articles
Radiopharmaceuticals: Why Now? | Why Is the Field Back in the Global Biopharma Spotlight?
Case Insight | What Does a Deal Worth Up to $1 Billion Reveal About Early CGT Validation?
A Practical Guide to CGT Clinical Trial Compliance: Key Points from Design to Inspection
Patient Recruitment and Retention Strategies in Chronic Ophthalmic Clinical Trials
Investigator-Initiated Trials (IIT): The Core Engine Accelerating Innovative Therapies from Bench to Bedside
GCP ClinPlus: Pioneering China's First Stem Cell Therapy Approval
China's Drug Approval Landscape is Accelerating: Partner with GCP ClinPlus to Navigate this Dynamic Market
Accelerating Innovative Cancer Treatment to Approval Executive Summary
Designing Compliant Clinical Trial Protocols for Innovative CGT Products: Key Considerations from a Clinical Design Perspective in the Pre-IND Stage
Case Study: Gene Therapy for Beta-Thalassemia (RM-001)
GCP ClinPlus Secures Series B Funding!
Study Kickoff Announcement | Treg Cell Therapy for ALS at Tiantan Hospital
Major Policy Boost for Innovative Drugs in China
FAQ: Conducting CGT Investigator-Initiated Trials (IITs) in China
Frequently Asked Questions: Clinical Operations in China for International Biopharmas
Why Global Biotechs are Turning to China for Clinical Trials: The Speed, Quality, and Cost Advantage
Global Biometrics Excellence: Powering Clinical Trial Success
Build or Buy? A Guide to Biometrics Resourcing
Interpreting the Roles and Responsibilities of Relevant Personnel from the Perspective of Clinical Trial Data Flow
Top 5 Biometrics Mistakes That Delay Clinical Trials
Checklist: How to Select a Biometrics Partner
Case Study: World's First 40kD Y-PEG Long-Acting Growth Hormone Approval
3 FDA Rejections You Can Avoid with Better Data Strategy
SDTM, ADaM or Define.XML: The Three Pillars of Data Standardization in Drug Development
Clinical Data Management Services
SAS Programming Services
Biostatistics Services
Biometrics in 2025: What Sponsors Need to Know Now
Avoiding Rework: How Intelligent Programming Saves Time in the Later Trial Phase
Navigating the Statistical Challenges of Rare Disease Clinical Trials
Case Study: Scalable Programming Excellence with FSP
Case Study: Strategic Clinical Oversight Accelerates Oncology Approval
Global Biometrics Excellence: A Decade-Long Partnership Driving Pharmaceutical Success
Ophthalmic Trial Endpoints and Centralized Imaging Evaluation
Expertise, Efficiency, Patients: Three Breakthroughs in Ophthalmic Rare Disease Gene Therapy Trials
CGT Operations Insight: Why Do Innovative Therapy Clinical Trials Require Long-Term Follow-Up and Data Governance?
Turning IIT Data into Scientific Outputs
PI Networks: A Strong KOL Does Not Equal a Delivery-Ready Network
Radiopharmaceutical Case Study: Pluvicto | From Approval to Access—Why Clinical Results Alone Do Not Determine Value
White Papers
China's CGT Market Opportunity: Accelerating Global Cell & Gene Therapy Development
8 Tech Trends Shaping Healthcare in 2026
Unlocking Opportunities: Ophthalmology Clinical Trials in China
China Hepatitis B and Liver Cancer Prevention and Treatment White Paper 2025
FAQs
Industry News
CROs on Fire: Davis Double Play Has Arrived
CXO Sector: Valuation Re-rating Under Way
FDA Crackdown on Trial Design: What July's CRLs to Replimune and Capricor Mean for Sponsors
The next chapter for China’s CAR-T industry: not just new indications, but a true test of execution precision.
Blog
Chinese Doctors’ Day | Honoring Every Physician Who Turns Clinical Questions into Better Answers
From Phase I to Phase III: China’s oligonucleotide pipeline is accelerating—but can clinical execution keep pace?
PI Network | Alzheimer’s Disease
World Brain Day | Brain Health Should Not Be a Privilege for the Few
World Skin Health Day | Better Knowledge. Better Skin Health.
Oncology Immunotherapy Trials | Dose Finding and CRS Management for Bispecific Antibodies
World ALS Day｜Breaking the Ice for Life: Challenges and Hope in ALS Clinical Trials
World Blood Donor Day｜Every Drop of Blood is the Foundation of Innovative Therapies
World Parkinson’s Day｜IIT Research: Unlocking New Possibilities in Neurodegenerative Diseases
Celebrating Another Milestone: Onradivir Tablets Approved
Why Partner with a China CRO for Global Cell and Gene Therapy Trials?
Unlocking Efficiency: A Guide to GCP ClinPlus's Clinical Operations Solutions
Mastering Compliance: GCP ClinPlus's Essential Guidelines for Clinical Data Management
Navigating Clinical Trials with Confidence: GCP ClinPlus's Phase-Specific Guidelines
GCP Insights – 7-Day Series | Key Updates: China's 2025 GCP Draft vs. 2020 Version (Day 1)
GCP Insights · Seven-Day Series | Is the 'Ethics Committee' Being Phased Out? 6 New Must-Know Terms for Day 1 (DAY 2)
GCP Insights · Seven-Day Series | Reshaping the Responsibilities of the Ethics Review Committee: Major Adjustments to Risk-Proportionate Review and Document Retention Periods (DAY 3)
GCP Insights · Seven-Day Series | Principal Investigator = The One to Blame? Decoding the Ultimate Responsibility Checklist with One Chart (DAY 4)
GCP Insights · Seven-Day Series | The Monitoring Chapter Vanishes: How to Write the Quality Management Plan in the RBM Era? (DAY 5)
GCP Insights · Seven-Day Series | A Brand-New Chapter is Born! GCP 2025 Establishes Principles for Data Lifecycle Management and Blinding Maintenance (DAY 6)
GCP Insights · Seven-Day Series | Streamlined Framework: GCP 2025 Shrinks from 9 Chapters & 83 Articles to 6 Chapters & 54 Articles – These Chapters Have Disappeared (DAY 7)
China's IIT Breakthrough: New Regulatory Clarity Opens Doors for Global Biopharma
GCP ClinPlus Named “Best Enabling Service Organization”
China Speed in CGT: From IND to NDA in 20 Months
China: A Competitive Destination for Global Radiopharmaceutical Clinical Trials
Reflecting on World Mental Health Day: Advancing Psychiatric Clinical Research with Compassion and Rigor
From the Lancet to NMPA Approval: GCP ClinPlus Accelerates Metabolic Drug Innovation
From Data to Approval: GCP ClinPlus Accelerates OT-702 with Al-Powered Execution
China's In Vivo CAR-T Landscape: Technology, Ecosystem, and Clinical Innovation Momentum
Expert Interview | Leveraging China's Clinical Resources to Build Faster, Smarter Global Clinical Trials
Expert Interview | Empowering Innovation, Navigating Complexity: GCP ClinPlus on the Statistical Science and Art of Anticancer Drug Clinical Trials
【Regional Outlook】Taking China-Originated Therapies Global: Can the Evidence Earn Trust Across Regions?
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GCP ClinPlus: Unlocking China's CGT Potential
GCP ClinPlus Company Video
GCP GlinPlus Clinical Biometrics Service Introduction Video
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Tel: +86 400-1006-531
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