Advancing Clinical Research: Lilly Centre for Clinical Pharmacology Pte Ltd
Based in Singapore, Lilly Centre for Clinical Pharmacology Pte Ltd (LCCP) is a leading clinical research organization (CRO) that specializes in early-phase clinical trials. With over 20 years of experience, LCCP has successfully conducted more than 1,000 studies for various pharmaceutical and biotechnology companies worldwide.
Comprehensive Services for Clinical Trials
LCCP offers a comprehensive suite of services to support all aspects of clinical trials, including:
- Study design and planning
- Patient recruitment and enrollment
- Data collection and management
- Statistical analysis and interpretation
- Regulatory submissions and approvals
- Medical monitoring and safety assessments
Focus on Early-Phase Trials (EPT)
LCCP specializes in early-phase clinical trials, which play a crucial role in drug development. EPTs help establish the safety, tolerability, and efficacy of new drugs in humans, providing valuable information to guide further clinical development.
State-of-the-Art Facilities
LCCP’s state-of-the-art clinical research unit in Singapore is equipped with:
- 50 dedicated beds
- 12 private patient rooms
- 14 monitoring rooms
- Ancillary facilities, including a laboratory, pharmacy, and medical imaging equipment
Renowned Team of Experts
LCCP’s team of experienced professionals includes:
- Clinical research scientists
- Medical doctors
- Data analysts
- Regulatory consultants
- Quality assurance personnel
Collaborations and Partnerships
LCCP actively collaborates with leading academic institutions, hospitals, and pharmaceutical companies to foster innovation and advance clinical research.
Commitment to Quality and Safety
LCCP is committed to the highest standards of quality and safety in clinical research. The organization is accredited by the Association for the Accreditation of Human Research Protection Programs (AAHRPP) and follows Good Clinical Practice (GCP) guidelines.
Meet the Needs of Pharmaceutical Companies
LCCP understands the challenges faced by pharmaceutical companies in drug development. We work closely with our clients to tailor our services to meet their specific needs, ensuring timely and cost-effective completion of clinical trials.
Key Numbers:
- 20+ years of experience
- 1,000+ clinical studies conducted
- 50 dedicated beds
- 95% success rate in patient enrollment
- 98% client satisfaction rate
Why Choose LCCP?
- Proven expertise in EPTs
- State-of-the-art facilities
- Dedicated and experienced team
- Commitment to quality and safety
- Flexibility and responsiveness
Benefits of Working with LCCP:
- Accelerate drug development
- Increase clinical study efficiency
- Ensure safety and ethical conduct
- Gain valuable insights into drug development
Let’s Innovate Together!
LCCP is always looking for ways to innovate and improve our services. We encourage you to connect with us and share your ideas. Let’s explore new possibilities and advance clinical research together.
Table 1:Lilly Centre for Clinical Pharmacology Pte Ltd Key Services
| Service | Description |
|---|---|
| Study Design and Planning | Collaborate with clients to develop study protocols, including objectives, design, and methodology. |
| Patient Recruitment and Enrollment | Identify and recruit eligible patients for clinical trials through various methods, including database screening and targeted advertising. |
| Data Collection and Management | Implement electronic data capture systems and ensure accurate and timely data collection and management. |
| Statistical Analysis and Interpretation | Perform statistical analysis of clinical data to draw meaningful conclusions and identify key trends. |
| Regulatory Submissions and Approvals | Prepare and submit regulatory submissions to obtain approvals from ethics committees and regulatory agencies. |
| Medical Monitoring and Safety Assessments | Monitor patients’ safety and well-being throughout the clinical trial and implement appropriate safety measures. |
Table 2: Lilly Centre for Clinical Pharmacology Pte Ltd Facilities
| Facility | Description |
|---|---|
| Dedicated Beds | 50 dedicated beds for patient stays during clinical trials. |
| Private Patient Rooms | 12 private patient rooms for increased privacy and comfort. |
| Monitoring Rooms | 14 monitoring rooms for continuous observation of patients. |
| Ancillary Facilities | Laboratory, pharmacy, and medical imaging equipment to support clinical trials. |
Table 3: Lilly Centre for Clinical Pharmacology Pte Ltd Team
| Role | Description |
|---|---|
| Clinical Research Scientists | Conduct clinical trials and collect, analyze, and interpret data. |
| Medical Doctors | Provide medical supervision and ensure patient safety throughout the clinical trial. |
| Data Analysts | Perform statistical analysis and generate meaningful insights from clinical data. |
| Regulatory Consultants | Guide clients through the regulatory approval process and ensure compliance with GCP guidelines. |
| Quality Assurance Personnel | Ensure the quality and integrity of clinical trial data and adherence to ethical standards. |
Table 4: Lilly Centre for Clinical Pharmacology Pte Ltd Collaborations and Partnerships
| Institution | Type of Collaboration |
|---|---|
| National University of Singapore | Joint research projects and student training. |
| Singapore General Hospital | Clinical trial recruitment and patient referrals. |
| Novartis | Early-phase clinical trials for oncology drugs. |
| Roche | Phase II clinical trials for autoimmune diseases. |
