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<\/figure><\/div>\n\n\n\nWe had been seeing the impact of site\/investigator identification on clinical trial successes time and again. A good beginning with the selection of quality, high recruitment sites is very likely to lead to successful clinical trial recruitment, patient selection, and quality data.<\/p>\n\n\n\n
Top 3 cost cutting and time saving techniques in initiating clinical trials<\/h2>\n\n\n\n- Performing regional feasibility (Country-level feasibility)<\/li>
- Analyzing clinical investigator, recruitment potentials, experience and site capabilities (Site\/investigator-level feasibility)<\/li>
- Thorough understanding of regulatory pathways and timelines <\/li><\/ul>\n\n\n\n
To follow these techniques, you need a huge connected database of clinical trial investigators and sites worldwide, such as a global centralized database.<\/p>\n\n\n\n
A global centralized database<\/h1>\n\n\n\n
In today’s era, while trial managers pay great attention to site selection and identification, their choices are mostly limited to their in-house databases, peer referrals, and\/or other search routes. This limitation may become very big if the project is planned in another country or therapeutic area than what trial teams generally work in.<\/p>\n\n\n\n
A central database available to trial managers at a very affordable cost can go a long way in ensuring trial successes and extending cost\/time – saving support to trial management teams.<\/p>\n\n\n\n
This fact had a great impact on Credevo founder, Dr. Kshitij Soni, and inspired him to start conceptualizing an online clinical research platform that can help in investigator identification. In a <\/span>LinkedIn article<\/span><\/a>, Kshitij shared his thoughts about developing such a centralized clinical research platform.<\/span><\/p>\n\n\n\n
\n\n\n\nExplore a wide range of Credevo services for your clinical trials<\/a><\/div>\n\n\n\n
\n\n\nCredevo<\/h1>\n
Credovo, currently is one of the fasted growing networks of clinical sites and investigators which can help trial managers reach 110000+ investigators, 55000+ sites, in 25+ countries around the world.<\/p>\n
![\"sites_investigators_credevo\"](\"https:\/\/credevo.com\/articles\/\/wp-content\/uploads\/2017\/10\/sites_investigators_credevo.jpg\")
<\/p>\n
It provides you with a tool to save more than 80% of cost and time in investigator and site selection.<\/p>\n
How does Credevo save 80% of cost and time<\/h1>\nCost – Saving<\/h2>\n
An offline feasibility assessment (site\/investigator level & country-level feasibility) for clinical trial usually costs from $200 – $300, from building database and contacting investigators to following up investigators and other expenses. With Credevo, it will only take less than $ 20 and even free in some cases to perform these processes.<\/p>\n
Time – Saving<\/h2>\n
It\u2019s the Credevo Feasibility Engine and Feasibility Team which will take care of everything. All you need to do is post your project with few required details on the Credevo website<\/a>.<\/p>\nNo need to develop your own database<\/h2>\nInvestigator Database<\/h3>\n
Credevo has an ever-increasing database of investigators and sites that can be accessed very conveniently. Credevo team also makes a consistent effort to increase this database, so that our clients and their team can get to assess feasibility with investigators in a way that is not possible with the locally available database.<\/p>\n
Making it easy for you<\/h2>\nEase of Working<\/h3>\n
Once you post your project, Just wait for investigators to respond with preliminary feasibility. Then simply choose to contact them or explore detailed feasibility with them.<\/p>\n
Credibility<\/h3>\n
Credevo ensures the reliability and qualification of investigators. Trial managers can also check all the required details through the feasibility questionnaire during the process.<\/p>\n
Confidentiality<\/h3>\n
Preliminary information is the only information shown on projects. The clinical trial manager chooses to share the synopsis and feasibility questionnaire with investigators that they want and that too under an NDA.<\/p>\n
No Country is a Barrier<\/h3>\n
Credevo currently has solid networking in place, in about 25 countries; and is up for any project for countries beyond the stated regions.<\/p>\n
All Major Therapeutic Areas<\/h3>\n
Whether it be oncology, infectious diseases, diabetes, dermatology, respiratory, or other major therapeutic areas for clinical development, Credevo will always strive to find you qualified, willing, and expert clinical trial investigators.<\/p>\n
How to get access to this network?<\/h1>\n
There are two easy ways to start.<\/span><\/p>\n\n- Just sign up on Credevo, and post your project with the required preliminary information. Credevo team will help you in further process.<\/span><\/li>\n
- In case, you have some queries before you’re ready to start, talk to us. You can also reach us on feasibility@credevo.com<\/a>.<\/span><\/li>\n<\/ol>\n\n\n
\n\n\nDo you need any other support for your clinical trial?<\/h2>\n
Credevo provides a wide range of innovative development strategies, country-level, and site-level feasibility studies, global regulatory support and clinical trial monitoring services worldwide for all your products, ranging from simple to complex ones.<\/p>\n
To follow these techniques, you need a huge connected database of clinical trial investigators and sites worldwide, such as a global centralized database.<\/p>\n\n\n\n
A global centralized database<\/h1>\n\n\n\n
In today’s era, while trial managers pay great attention to site selection and identification, their choices are mostly limited to their in-house databases, peer referrals, and\/or other search routes. This limitation may become very big if the project is planned in another country or therapeutic area than what trial teams generally work in.<\/p>\n\n\n\n
A central database available to trial managers at a very affordable cost can go a long way in ensuring trial successes and extending cost\/time – saving support to trial management teams.<\/p>\n\n\n\n
This fact had a great impact on Credevo founder, Dr. Kshitij Soni, and inspired him to start conceptualizing an online clinical research platform that can help in investigator identification. In a <\/span>LinkedIn article<\/span><\/a>, Kshitij shared his thoughts about developing such a centralized clinical research platform.<\/span><\/p>\n\n\n\n Credovo, currently is one of the fasted growing networks of clinical sites and investigators which can help trial managers reach 110000+ investigators, 55000+ sites, in 25+ countries around the world.<\/p>\n It provides you with a tool to save more than 80% of cost and time in investigator and site selection.<\/p>\n An offline feasibility assessment (site\/investigator level & country-level feasibility) for clinical trial usually costs from $200 – $300, from building database and contacting investigators to following up investigators and other expenses. With Credevo, it will only take less than $ 20 and even free in some cases to perform these processes.<\/p>\n It\u2019s the Credevo Feasibility Engine and Feasibility Team which will take care of everything. All you need to do is post your project with few required details on the Credevo website<\/a>.<\/p>\n Credevo has an ever-increasing database of investigators and sites that can be accessed very conveniently. Credevo team also makes a consistent effort to increase this database, so that our clients and their team can get to assess feasibility with investigators in a way that is not possible with the locally available database.<\/p>\n Once you post your project, Just wait for investigators to respond with preliminary feasibility. Then simply choose to contact them or explore detailed feasibility with them.<\/p>\n Credevo ensures the reliability and qualification of investigators. Trial managers can also check all the required details through the feasibility questionnaire during the process.<\/p>\n Preliminary information is the only information shown on projects. The clinical trial manager chooses to share the synopsis and feasibility questionnaire with investigators that they want and that too under an NDA.<\/p>\n Credevo currently has solid networking in place, in about 25 countries; and is up for any project for countries beyond the stated regions.<\/p>\n Whether it be oncology, infectious diseases, diabetes, dermatology, respiratory, or other major therapeutic areas for clinical development, Credevo will always strive to find you qualified, willing, and expert clinical trial investigators.<\/p>\n There are two easy ways to start.<\/span><\/p>\n Credevo provides a wide range of innovative development strategies, country-level, and site-level feasibility studies, global regulatory support and clinical trial monitoring services worldwide for all your products, ranging from simple to complex ones.<\/p>\n
\n\n\n\n
\n\n\nCredevo<\/h1>\n
<\/p>\nHow does Credevo save 80% of cost and time<\/h1>\n
Cost – Saving<\/h2>\n
Time – Saving<\/h2>\n
No need to develop your own database<\/h2>\n
Investigator Database<\/h3>\n
Making it easy for you<\/h2>\n
Ease of Working<\/h3>\n
Credibility<\/h3>\n
Confidentiality<\/h3>\n
No Country is a Barrier<\/h3>\n
All Major Therapeutic Areas<\/h3>\n
How to get access to this network?<\/h1>\n
\n
\n\n\nDo you need any other support for your clinical trial?<\/h2>\n