UNCOMMON
PRE-CLINICAL AND CLINICAL
CRO BASED IN INDIA
SOLUTIONS PARTNER
from Pre-clinical to clinical research
AND CLINICAL EXPERIENCE
GREAT TECHNOLOGY.
GREAT FLEXIBILITY
EXPERIENCED TEAM
A dedicated human team with over 10 years of experience and a high priority to quality improvement and timelines. They are our most important asset and what make an enormous difference to your studies.
QUALITY SERVICES
Following a rigorous internal quality system which meets international regulatory guidelines, and also using state-of-the-art methods and systems in biostatistics and data management. The most efficient procedures to guarantee your success.
FOCUS ON CLIENTS
We offer the experience of an international company with the tailored service of a local enterprise which adds a great value to your projects. Working side-by-side and sharing the risks is the only way to be a real partner.
FLEXIBILITY
It is our self-demand to have the flexibility to adapt our services to the client requirements, within the framework of the GCP/ICH and our own SOPs and quality system.
In a global word with global studies, we know better how to adapt to the local requirements
About us
WE’RE HERE TO CHANGE THE WAY THE WORLD ENCOUNTER CRO'S, IN THE BEST POSSIBLE SOLUTIONS.
Krescent Medical Research is a full service pre-clinical and Clinical Research Organization (CRO) that supports pharmaceutical, biotechnology and medical device companies throughout their entire drug development journey. Also, as a collaborator it’s our duty to guide you through the complexities of the drug development and regulatory submission process. We impart strategic decision-making and operational support for your pre-clinical, clinical trials and regulatory submission projects by truly creative, innovative, and scientific thinkers.
We are a passionate drug development organization committed to improving medical research model by offering quality professional services with low overhead at justifiable, competitive industry pricing.
Solutions
We try to serve best solutions
Lorem ipsum dolor sit amet consectetur adipiscing elit sed do eiusmod tempor incididunt ut labore et dolore magna.
FAQ
FAQ form Krescent
You will learn more from FAQ
WHAT IS KRESCENT MEDICAL RESEARCH?
We are full-service preclinical and clinical Contract Research Organization, our solutions include all the activities from design, setting up and monitoring of preclinical/clinical trials and research studies, up to the management of data, statistical analysis and medical writing, covering the whole process to introduce new medical devices and pharmacy products on the market, and a Site management services covering Asia pacific region, during the study and once the marketing authorization is available.
HOW DO YOU SELECT SITE’S FOR CLINICAL TRIAL?
Through our investigation department and the medical team we offer our support to select the principal investigators and KOLs for each therapeutic area and warranty their commitment with the study.
We already have created links and laces with the investigators we have worked with, that let us count on with their confidence to reach the success on every investigation we take part, being them our principal prescribers.
With this investigators database we could also help the sponsor to select the best sites all over India through our site selection system and database that ensure the feasibility of the services of the site (Pharmacy, Laboratory, Image Service, General Resources and Human Resources) according to the needs of the study.
We already have created links and laces with the investigators we have worked with, that let us count on with their confidence to reach the success on every investigation we take part, being them our principal prescribers.
With this investigators database we could also help the sponsor to select the best sites all over India through our site selection system and database that ensure the feasibility of the services of the site (Pharmacy, Laboratory, Image Service, General Resources and Human Resources) according to the needs of the study.
HOW DO YOU DESIGN AND PLAN FOR CLINICAL TRIALS?
We help our sponsors on the definition of the investigation best design, according to parameters such as a drug safety, study feasibility, best approval strategies, validity, science interest, and of course the investment profitability.
Necessary intelligence and creativity are applied on developing a global strategy which helps on saving resources to implant the medicine in the major markets possible, considering that a good global planning avoids duplicating efforts at the same time that simplifies the adaptation to the international standards to the specifics regulations of each country.
We share the knowledge of our experts on design effective programs that allows the adaptation to each country regulations and an optimal distribution of the medicinal devices and pharmacy products.
Necessary intelligence and creativity are applied on developing a global strategy which helps on saving resources to implant the medicine in the major markets possible, considering that a good global planning avoids duplicating efforts at the same time that simplifies the adaptation to the international standards to the specifics regulations of each country.
We share the knowledge of our experts on design effective programs that allows the adaptation to each country regulations and an optimal distribution of the medicinal devices and pharmacy products.
HOW DO YOU GET WORK DONE FROM REGULATORY AGENCY/EC?
We have a wide applied experience on the intermediation process between the internal regulatory affairs department and the government agencies and competent authorities (Local, Autonomic and country) to reach the approval of the different studies and trials, simplifying the whole process and reducing the costs associated to this activity.
We work and count on with and extend net of sites and their Ethics Committees, that allows us to warranty the minimum consumption of needed resources to get the EC approval in each project we became involved.
Necessary intelligence and creativity are applied on developing a global strategy which helps on saving resources to implant the medicine in the major markets possible, considering that a good global planning avoids duplicating efforts at the same time that simplifies the adaptation to the international standards to the specifics regulations of each country.
We work and count on with and extend net of sites and their Ethics Committees, that allows us to warranty the minimum consumption of needed resources to get the EC approval in each project we became involved.
Necessary intelligence and creativity are applied on developing a global strategy which helps on saving resources to implant the medicine in the major markets possible, considering that a good global planning avoids duplicating efforts at the same time that simplifies the adaptation to the international standards to the specifics regulations of each country.
Still have any query please Contact us
Team
MEET THE PEOPLE WHO LEAD THE WAY TO A BETTER CLINICAL EXPERIENCE
At Krescent, our employees provide the support, structure, and professional background for better pre-clinical and clinical research.
Meet the people who lead the way to a better clinical experience.
Testimonials
Some reviews from our clients
Blog
Some from our latest news
We would love to share a similar experience and how I
learned some valuable lessons during a downturn.
05 Nov 2019
Strategy for Norway’s Peion to Fund Global.
A new study finds the value of using 'parentese,' an exaggerated speaking style that conveys total engagement with.
Call for 24 hours / 7days 2417
CLIENTS
OUR CLIENTS
