Curexbio is a Clinical Research Organization (CRO) that provides comprehensive trial management services to ensure efficiency, compliance, and success across all phases of clinical studies, from early development to post-market surveillance.

What core services does Curexbio offer to support clinical trials?

Curexbio offers a robust suite of services including comprehensive clinical trial management, strategic clinical development, diligent clinical monitoring, and extensive pharmacovigilance, all designed to streamline and enhance the success of your clinical studies.

How does Curexbio ensure patient safety and ethical compliance in clinical trials?

Curexbio prioritizes patient welfare through vigilant pharmacovigilance, strict adherence to ethical guidelines, and rigorous monitoring protocols. We ensure all studies comply with international standards like ICH-GCP, safeguarding participant rights and well-being.

What are the advantages of partnering with Curexbio for clinical research?

Partnering with Curexbio offers numerous advantages, including access to our expertise-driven approach, streamlined trial management for efficiency, assured regulatory compliance, and a client-focused collaboration model designed to achieve successful outcomes and accelerate market approval.

Which phases of clinical studies does Curexbio support?

Curexbio provides comprehensive support across all phases of clinical studies, from early-phase clinical development and initial monitoring through to late-stage trials and crucial post-market pharmacovigilance.

How does Curexbio ensure data quality and integrity in clinical trials?

Curexbio maintains high data quality and integrity through meticulous clinical monitoring, robust data management practices, and strict adherence to regulatory guidelines. Our processes are designed to ensure accuracy, reliability, and security of all collected data.

What is Curexbio's approach to regulatory compliance?

Curexbio integrates regulatory compliance into every aspect of its clinical operations. We stay abreast of evolving global and local regulations, ensuring all studies are conducted and documented in full accordance with the latest scientific and regulatory standards.

Does Curexbio offer customized solutions for specific client needs?

Yes, Curexbio prides itself on a client-focused approach. We work collaboratively with each client to understand their unique needs and challenges, offering customized clinical trial management and development solutions tailored to specific project requirements and therapeutic areas.

Safety & Pharmacovigilance Services

At Curex, we deliver tailored pharmacovigilance services using advanced safety data systems to ensure accuracy, minimize risk, and prioritize subject safety.

Safety Isn’t Optional, it forms the pillar for success of clinical trial.

At CUREXBIO, our end-to-end pharmacovigilance services and expert consulting ensure strict adherence to global regulations and proactive risk mitigation throughout the drug development process. We prioritize drug safety through quality-driven and adaptable solutions, enabling international regulatory compliance. Our specialized pharmacovigilance services help manage safety concerns early, minimizing potential delays and challenges.

Our Expertise in Pharmacovigilance Services Includes:

Individual Case Safety Report (ICSR) processing and identification: At CUREXBIO, we ensure accurate collection, processing, and identification of ICSRs to maintain patient safety and regulatory compliance.
Regulatory submissions (DSUR, PSUR/PBRER, PADER/PAER, periodic reports) : The basis to meet regulatory standards and compliance, is the timely preparation and submission of periodic safety reports
Literature monitoring: To identify potential and emerging safety information for ongoing PV, CUREXBIO supports continuous monitoring of medical and scientific literature.
Safety data evaluation and signal detection: To detect safety signals and enabling proactive risk management, CUREXBIO evaluates the safety data on demand.
Safety database configuration and oversight (Oracle Argus or client platforms): For ensuring data integrity and compliance with global standards, CUREXBIO configures and manages safety databases.
Benefit-risk analysis and risk management planning: To improve patient safety, we perform stringent benefit-risk analysis and implement risk management plans.
EudraVigilance assistance : Assuring seamless communication with European Authorities with timely reporting and maintaining compliance with EudraVigilance
In-licensed and out-licensed products management: CUREXBIO supports lifecycle management and market compliance by overseeing safety and regulatory obligations for licensed products.

We offer support for clients, ensuring seamless pharmacovigilance management from first-in-human trials to post-marketing phases. Our expert team and recognized processes fulfil compliant, superior safety reporting, constantly and on schedule.

CUREXBIO’s Key Strengths:

Expert safety team: A highly qualified team ensures efficient, high-quality case processing.
Effective reporting standards: Regulatory-compliant, audit-ready reports with robust KPIs and proven reliability.
Rapid case processing: Swift, unblinded ICSR reporting while preserving study integrity.
Proactive risk management: Ongoing safety monitoring, signal detection, and literature reviews.
Regulatory expertise: Current knowledge of country-specific regulatory requirements.
Seamless database transitions: Proficiency in secure, smooth safety database migrations.

Our experts offer business continuity through consistent safety reporting and on-time safety operations, enabling clients to focus on advancing drug development programs with confidence—backed by CUREXBIO’s reliable pharmacovigilance services.

Our Expertise Includes:

Why Choose Curexbio for Safety and Pharmacovigilance?

Trusted PV Experts

Dedicated in-house team of experienced PV professionals.

Tech-Driven Safety

Use of latest safety technologies for streamlined reporting.

Global PV Compliance

Proficient in global regulatory requirements and electronic systems.

Timely & Accurate PV

Commitment to timely, accurate, and high-quality PV services.

Request For Proposal

We offer an array of niche and full-fledged CRO services, from clinical trial protocol development to post-marketing surveillance. Streamline Your Drug Development with Curexbio CRO Expertise

Curexbio Insights Hub

Dive into the latest research, insights, and innovations with our team of experts in the fields that matter most to clinical advancement.

CurexBio specializes in efficient, compliant clinical trials across all phases. We blend scientific expertise with advanced technologies to accelerate drug development. From study design to data management and reporting, our team ensures accuracy, regulatory compliance, and patient safety. With a focus on innovation and collaboration, CurexBio is your trusted partner in turning research into real-world treatments.

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1113, Silver Radiance 4 Sarkhej – Gandhinagar Hwy, Chanakyapuri, Ahmedabad, Gujarat 382481
bd@curexbio.com
+91 8905818034
+91 7784847766
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