Clinical Development Strategy

Credevo provides high-level strategic consulting services ranging from clinical trial design and protocol development to regulatory submission with various regulators worldwide

Our services


We specialize in providing comprehensive services to help with your clinical drug development strategy. This includes support during the early stages of clinical development along with regulatory strategy build up. This is further aided by support during late stages with progress in your clinical development program.

Clinical Development

The clinical development process requires well-structured planning and is often complex and risky,  which can cost your organization significant time and money.

Credevo with a dedicate team offers expertise in clinical development with a single point of contact, accountability, transparency, and has a track record of successful delivery within determined timelines

Drug development in rare diseases is critical compared to traditional drugs and requires special strategies and agile techniques. Credevo offers dedicated expertise in rare disease drug development

Learn more on rare Disease Drug Development Strategies

Strategic and Regulatory Planning

A regulatory strategy is a plan of action designed to achieve a specific regulatory goal, such as to obtain approval or clearance of a new product & Regulatory plan is a document illustrating the specific actions that are needed to meet the regulatory strategy objectives successfully

Credevo offers regulatory development strategy, clinical trial and marketing authorization submissions with a vastly experienced team and successful track records in strategic and regulatory planning

Click here to understand Global Regulatory Pathways For Clinical Development Strategy

Global project management

Managing a clinical trial project requires expertise along with prominent experience and skills that lead in producing efficient and comprehensive data to reach the predetermined goals

Credevo owns and intimately engages in every aspect of your clinical trial. You can just rely on your Project Management team in capturing all relevant data to support your study goals

Learn more on ‘Software and Data Management Tools in Clinical Trials’


Investigator recruitment and site management

70% of trials fail due to inefficient clinical investigator and site selection – Credevo has a huge database of clinical investigators and sites worldwide. Based on the study requirements, Credevo recruits the most efficient clinical investigators and qualified sites. And has a track record even in rare disease clinical trials


Patient recruitment and retention strategies

Recruiting sufficient subjects for the study and maintaining retention is the nightmare in the clinical trial industry and requires techniques and well-structured strategies to conceive

Credevo designs an adaptive strategy and novel techniques to attain complete patient recruitment, and implements right from the protocol design to study completion

Rare disease clinical trials offer many more challenges compared to traditional drugs and medical devices. Credevo offers its expertise to overcome these challenge and complete the trials within time

Learn more on ‘How to Improve Patient Recruitment in Clinical Trials


Clinical monitoring

Efficient management and monitoring of clinical sites are critical to a successful clinical trial and ensure that the trial is conducted according to the protocol, GCP, SOP, and regulatory requirements

Credevo services are tailored to your needs and offer a comprehensive clinical trial monitoring and site management services right from clinical feasibility through study completion to support clinical trials around the world. We have globally connected networks and manage your trials anywhere in the world


Global feasibility studies

Conducting clinical trial feasibility is crucial for any clinical trial to understand the clinical investigator and site capabilities, patient recruitment potential, timelines, and many more to prevent clinical trial failures or delays

Credevo provides a very intuitive and efficient web-based platform to connect with thousands of clinical investigators and sites worldwide. Connect with clinical investigators, conduct feasibility, review and select with just a few simple steps

Learn more on ‘Why Clinical Trial Feasibility is an important tool before you conduct a clinical trial’

Credevo also offers country-level and site-level feasibility studies in rare disease clinical trials which are crucial to perform before initiating a clinical trial to avoid failures or delays

Acute Myeloid Leukemia, Glomerulonephritis, Amyotrophic Lateral Sclerosis, Alopecia areata, and many more


Mail your queries at helpdesk@credevo.com, or provide the details below and our team will get back to you





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