welcome to MediCRO Research
We Manage Clinical Trials From Start To Finish
OUR PARTNERS
Area of Practice
01
Clinical Trial Management
We will work with you to create a personalised plan to help you achieve your financial goals.
02
Audit Preparedness
We will work with you to create a personalised plan to help you achieve your financial goals.
03
Regulatory compliance
We will work with you to create a personalised plan to help you achieve your financial goals.
04
Site Staf Training
We will work with you to create a personalised plan to help you achieve your financial goals.
05
Patient Recruitment
We will work with you to create a personalised plan to help you achieve your financial goals.
06
Data Management
We will work with you to create a personalised plan to help you achieve your financial goals.
Ethical standard and regulatory requirement
We understand the importance of conducting high-quality research that meets ethical standards and regulatory requirements. That’s why we work closely with our clients to develop customized solutions tailored to their specific needs and goals. Whether you are looking to participate in new clinical trial as a site, optimize an existing study, or expand your research portfolio, we can provide the expertise and support you need to succeed.
Be onboard with trained and accredited professionals
we partner with healthcare professionals, pharmaceutical companies, academic institutions, and medical device manufacturers to ensure the successful planning, execution, and management of clinical trials and research studies.
★ ★ ★ ★ ★
My experience at the restaurant was great. The food was delicious, the service was excellent, and the atmosphere was cozy and inviting. Highly recommend this restaurant.
Alex Martinez
/
Customer
We make clinical trail easy.
✓ Easy and straightforward process
✓ Flawless management, analysis and reporting
How We Work
Work Process
01
Data Management
We will work with you to create a personalized plan to help you achieve your financial goals.
02
Quality Assurance
We will work with you to create a personalized plan to help you achieve your financial goals.
03
Audit Preparedness
We will work with you to create a personalized plan to help you achieve your financial goals.
Success
Proven track of successfully resolved cases for over 20 years
12k
Clients
20
Years
Who are we
We promote diversity across all projects
✓ Merit Based Hiring
✓ Diversity and inclusion
Testimonials
Our Customers Said
★ ★ ★ ★ ★
4.85 from 1,300+ reviews
“Delizioso”
A must try for all Italian food lovers! The best Italian restaurant I’ve ever been to! Highly recommended!
★ ★ ★ ★ ★
— Martha Nazario
“Authentic Flavour”
The pasta dishes are cooked to perfection and the sauces are full of flavour. Highly recommend!
★ ★ ★ ★ ★
— Alex Martinez
“Outstanding Pizza”
The crust is thin, the sauce is flavourful and the toppings are very fresh. Will come again for sure.
★ ★ ★ ★ ★
— Antoine Crawford
Have Questions?
Frequently Asked
Questions
What is Audit Preparedness in clinical trials?
Audit Preparedness refers to the process of having all necessary documentation and procedures in place to ensure compliance with regulatory requirements and standards during an audit by regulatory authorities. This includes record-keeping, protocol adherence, and data management practices.
How can I ensure Regulatory Compliance in clinical trials?
To ensure regulatory compliance in clinical trials, it is important to stay up-to-date on the latest regulations and guidelines set forth by regulatory authorities such as the FDA and EMA. This includes having thorough protocols in place, obtaining proper informed consent from participants, maintaining accurate and complete records, and adhering to Good Clinical Practice (GCP) guidelines.
What is Data Management in the context of clinical trials?
Data Management in clinical trials refers to the collection, storage, and analysis of data generated during the trial. This includes ensuring the accuracy and integrity of the data, protecting participant confidentiality, and maintaining compliance with data protection regulations.
How can I improve Data Management practices in my clinical trial?
To improve Data Management practices in your clinical trial, consider implementing electronic data capture systems, conducting regular data quality checks, providing adequate training to staff on data entry procedures, and establishing clear data management SOPs.
What is the role of a Clinical Trial Manager in Audit Preparedness?
The Clinical Trial Manager plays a crucial role in Audit Preparedness by overseeing the implementation of quality assurance and quality control measures throughout the trial. This includes conducting regular audits of trial documentation, addressing any compliance issues that arise, and ensuring that the trial is conducted in accordance with regulatory requirements.
How can I prepare for a regulatory audit of my clinical trial?
To prepare for a regulatory audit of your clinical trial, make sure all trial documentation is up-to-date and readily accessible, conduct internal audits to identify and address any compliance gaps, and ensure that all staff involved in the trial are trained on audit procedures and regulations.
What are common challenges in Audit Preparedness for clinical trials?
Common challenges in Audit Preparedness for clinical trials include inadequate documentation, poor data management practices, lack of staff training on regulatory requirements, and changes in regulatory guidelines that may impact trial conduct. Remember, it is important to consult with regulatory experts and experienced clinical trial managers to ensure that your trial is conducted in accordance with all regulatory requirements and best practices.
Need more information?
Struggling to find the answers you need? Let’s have a conversation.