eChinaChem, Inc., the China subsidiary of Pacific Genuity, Inc. (San Carlos, California), provides an integrated...
Data Management & Biostatistics Project Management and Monitoring (Local and International) Site Management & GCP/ICH-GCP Training Product Development Strategy & Marketing Research Academic Meeting ...
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SOP system has passed the UK and Japanese standard Audit. Can work in Japanese and English
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 ...
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 ...
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 ...
Successful medical product development and registration requires a sophisticated regulatory strategy supported by timely availability of high quality regulatory documentation and effective communication ...
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 ...
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 ...
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 ...
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 ...
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 ...
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 ...
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'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 ...
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 ...
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
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 ...