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 the late stages of 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 dedicated team offers expertise in clinical development with a single point of contact, accountability, and 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 investigators 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 a 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 challenges and complete the trials within the 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 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
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 to inquiry@credevo.com, or provide the details below and our team will get back to you