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Clinical Operations Solutions for Global Pharmaceutical Innovation

At GCP ClinPlus, our Clinical Operations team serves as the cornerstone of our full-service CRO offerings, providing end-to-end clinical trial management with precision, speed, and regulatory excellence. With over 2,200 clinical projects supported and 210 NDA approvals—including 4 FDA/EMA approvals—we are a trusted partner for sponsors seeking to navigate China's dynamic clinical research landscape.
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Comprehensive Support Throughout Your Clinical Journey

Our Clinical Operations services encompass every phase of trial execution:
Site Feasibility & Selection

Leveraging our network of over 1,400 GCP-compliant research sites across China, we identify and initiate high-performing sites tailored to your study needs.

Site Feasibility & Selection
Study Start-Up (SSU)

Efficiently managing center screening, regulatory submissions, and site initiation to accelerate trial commencement.

Study Start-Up (SSU)
Patient Enrollment & Retention

Implementing strategies to optimize patient recruitment and maintain engagement throughout the study.

Patient Enrollment & Retention
Clinical Monitoring

Conducting regular site visits and remote monitoring to ensure protocol adherence, data integrity, and patient safety.

Clinical Monitoring
Data Management Support

Collaborating closely with our data management team to facilitate timely data cleaning and query resolution.

Data Management Support
Site Management & Close-Out

Overseeing site operations to ensure compliance and managing the close-out process efficiently.

Site Management & Close-Out

Why Choose Our Clinical Operations Solutions?

  • Access to Treatment-Naïve Populations: Facilitating enrollment by tapping into China's vast patient pool.

  • Regulatory Expertise: Navigating NMPA's accelerated approval pathways with proven success.

  • Cost Efficiency: Delivering high-quality services at 30–40% lower costs compared to US/Europe.

  • Expedited Timelines: Achieving faster patient recruitment and study completion.

    By integrating local insights with global standards, GCP ClinPlus ensures that your clinical trials in China are conducted with the highest levels of quality, compliance, and efficiency.

100%
Global Sponsor Audit Pass
100+
NMPA Inspections Passed
100+
CRAs, 80% with life sciences background
22+
years' experience

Patient Enrollment Strategies

Fast, Targeted Patient Enrollment in China: Leveraging a vast patient pool, top hospital networks, trusted PIs, and patient group partnerships to enroll the right patients—on time, every time.

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Testimonials of GCP ClinPlus

Head of Biometrics, Leading Biotech
Head of Biometrics, Leading Biotech
"

GCP ClinPlus delivers exceptional expertise with genuine commitment to our projects. Their team demonstrates remarkable responsibility at every stage, consistently going above and beyond. In an industry where dedication matters, they've proven themselves an invaluable partner for our success.

"
VP of Clinical Development, Biotech
VP of Clinical Development, Biotech
"

After enrollment challenges with our previous CRO threatened our study timeline, GCP ClinPlus stepped in and transformed our project. Their team rapidly accelerated patient recruitment beyond our expectations and put our critical study back on track. Their clinical expertise and swift implementation proved decisive in securing our study's success.

"
Project Manager, Pharmaceutical Company
Project Manager, Pharmaceutical Company
"

GCP ClinPlus stands out for their exceptional responsiveness and customer focus. Their team consistently prioritizes our needs with prompt, thoughtful solutions to every challenge. Their combination of technical excellence and client-centered approach makes them a truly strategic partner in our development programs.

"
Regulatory Intelligence
Real-time tracking of global pharmaceutical regulatory updates, in-depth interpretation of the latest FDA, EMA, NMPA guidelines to help you accurately control R&D compliance.
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Cases & Articles
Unveiling practical experience from clinical projects, sharing benchmark cases in oncology, CGT and other fields, providing reusable industry insights and solutions.
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White Papers
Access to thematic white papers, unlocking cutting-edge technology methodologies and data insights.
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Focus on innovation trends, share industry observations, empower scientific decision-making.
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2005 Eastpark Blvd., Cranbury, New Jersey, USA, 08540
Headquarters Address:
Building 1, Hanwei International Zone 3, 186 South Fourth Ring West Road, Fengtai District, Beijing
Tel: +86 400-1006-531
global@GCP-ClinPlus.com +1 609-2553581
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