Find clinical trials to work as investigator

Clinical research is an indispensable section of human healthcare today. It forms the major part of any drug development effort and thousands of doctors and scientists worldwide actively engage in it. Trial Managers – Investigators Trial managers, monitors, research associates, site specialists, site identification and selection teams are always in search of experienced, qualified, and […]

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Clinical trial regulatory and approval process in Thailand

Thailand furnishes a good infrastructure, and a robust and flexible regulatory process to conduct clinical trials. There is a rise in the interest of many pharma companies and research organizations in conducting clinical trials in Thailand. Continuation from Clinical Trial Regulatory & Approval Process In Thailand (Part-1). We often receive queries from pharmaceutical companies and clinical […]

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Clinical trial regulatory and approval process in Thailand

Among 10 ASEAN countries, Thailand registers the highest number of clinical trials in the region, and the number of BA/BE studies is increasing. The regulatory process and requirements to conduct clinical trials in Thailand are of interest to many pharmaceutical companies. We often receive queries from pharmaceutical companies and clinical research organizations asking about the […]

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Credevo founder will Be a Speaker at an event called La French Tech Thailand on Wednesday 7th September 2016 at The Hive, Bangkok. The theme of the event is MedTech – A focus on the medical technology. Dr Kshitij Soni, PhD: Clinical Drug Development – easier, faster and more affordable way. Founder of Credevo.com, an innovative global clinical development […]

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Undoubtedly, the most critical roles in any clinical trial are the ones played by the investigators and site support staff. They’re the team that actually perform the activities leading up to or structuring an investigation of drug effects and safety. At Credevo.com, we strive to connect talented investigators and sites with new clinical trials requirements. […]

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