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Product Name |
Product Description |
Company Name |
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CRO FULL-SERVICE
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Data Management & Biostatistics
Project Management and Monitoring (Local and International)
Site Management & GCP/ICH-GCP Training
Product Development Strategy & Marketing Research
Academic Meeting ... |
Rundo Cronova International Clinical Research Co.,LTD |
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Clinical Data Management
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Shanghai Careway Medi-pharm Technology Co.,Ltd |
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Data Management and Statisitics
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SOP system has passed the UK and Japanese standard Audit. Can work in Japanese and English |
Rundo Cronova International Clinical Research Co.,LTD |
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Monitoring
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Accelovance (China) operates to deliver ICH-GCP compliant clinical trials. Its staff has strong experience in conducting ICH-GCP clinical trials for multinational client and it utilizes the same clinical ... |
Accelovance (China) Co., Ltd. |
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Regulatory Service
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Accelovance (China) operates to deliver ICH-GCP compliant clinical trials. Its staff has strong experience in conducting ICH-GCP clinical trials for multinational client and it utilizes the same clinical ... |
Accelovance (China) Co., Ltd. |
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Data Management/Statistics
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Accelovance (China) operates to deliver ICH-GCP compliant clinical trials. Its staff has strong experience in conducting ICH-GCP clinical trials for multinational client and it utilizes the same clinical ... |
Accelovance (China) Co., Ltd. |
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Biostatistics
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The department of biostatistics of Tigermed is managed by the chief statistician who is one of the menbers of Drug Evaluation Committee of SFDA.Tigermed owns experienced professionals of data management ... |
Hangzhou Tigermed Consulting Co., Ltd. |
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Data Management
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1. Phase I-IV Clinical Studies
2. Small and Large Studies
3. Stand-Alone Projects
4. Full-Service Clinical Programs
5. Flexible Data Collection and Entry Options – Using Our Systems or Yours
1) Paper ... |
Quintiles Transnational Corp. |
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Global Regulatory Affairs
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Successful medical product development and registration requires a sophisticated regulatory strategy supported by timely availability of high quality regulatory documentation and effective communication ... |
MDS Pharma Services (China) Inc. |
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clinical data management
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Unlike the rigid structure of other CROs, Kendle Biometrics provides you with a truly customized data management system to accommodate your specific needs.
For example, we can perform data management ... |
Kendle International Inc. |
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Date Management
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BOSOM evaluates the trial in the design phase in order to create an efficient data management process, specific to client requirements. In this way DAS can deliver a clean, locked database with a minimal ... |
Beijing BOSOM science and technology Co.,Ltd. |
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Regulatory Services
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PHDS has been profoundly devoted to its regulatory services since its foundation. With the accumulation of extensive experience on the regulatory due diligence process,PHDS’ regulatory experts are proficient ... |
BJ.PHDS Healthcare Research |
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Pharmacovigilance
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GleneaglesCRC offers services in pharmacovigilance to ensure that the safety information are collected during the study, processed and reported to the sponsor, the IRBs/IECs and regulatory authorities ... |
GleneaglesCRC Pte., Ltd. |
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Clinical Data Management
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Back End Services
1. Clinical Data Management
1) Data Logging and Tracking
2) Data Entry of Completed Case Report Forms (CRF)
3) Electronic and Manual Data Review/Query Issuance
4) Code thd Data ... |
GleneaglesCRC Pte., Ltd. |
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Clinical Data Management
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Committed to providing the accuracy of your valuable data, APEX goes to great depths to ensure the data provided to our sponsors are reliable without delay. This is only made possible through our multi-steps ... |
APEX International Clinical Research Co., Ltd. |
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Medical Affairs
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To ensure valid and robust outcomes of a clinical trial, the medical expertise at APEX get involved in the study in the earliest phase possible. This increases the overall efficiency and reduces the need ... |
APEX International Clinical Research Co., Ltd. |
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Regulatory Services
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APEX's regulatory team can provide the following benefit:
Regulatory Services
Plant Master File (PMF)/ Site Master File (SMF) application
Quality System Documentation (QSD) application
Good Manufacturing ... |
APEX International Clinical Research Co., Ltd. |
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Clinical Monitoring
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At APEX Clinical Research Co., our skilled professional team is fully capable of providing a complete range of clinical monitoring services. Depending on the needs of the clientele, APEX offers its services ... |
APEX International Clinical Research Co., Ltd. |
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Data Management
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1. CRF design and production
2. Data management plan
3. Database creation
4. Patient recruitment
5. Double data entry
6. Data coding
7. Data validation |
Essenix Pharmaceuticals, Inc. |
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Clinical Trial
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1. Protocol Design
2. CRF Design
3. Investigators (PT) Selection
4. Investigator's Brochure Preparation
5. Trial Organization and Management
6. Trial Monitoring and auditing
7. Serious Adverse Event ... |
Beijing Jionn Pharmaceutical Center |