Region Based Clinical Trials

Navigating the complexities of Phases I, II and III of your clinical trials can be challenging. Having a local partner that knows how to keep everything on track, on time and on budget is vital to the success of your study in Kali Clinical Research.

Our local-based knowledge, proven expertise and highly personalized services provide the solutions you need to meet multiple milestones, solve recruitment challenges, monitor safety and effectiveness.

With our Global Headquarters in Baja, Mexico, we offer first-hand knowledge of the region. This allows us to guarantee better results in patient recruitment when compared to our competitors.

How Clinical Trials Work

It’s important that drugs and medical treatments are safe and effective. Every approved medication, treatment or medical device available today has at some time been tested in a clinical trial (and often more than one). 

We conduct clinical trials to predict how well a medication or therapy will perform in the general population when used to treat a certain condition. Sometimes medications or treatments used for one purpose may be tested again to see if they can treat additional conditions.

Our clinical trials measure the safety and effectiveness of a proposed medication or treatment, compared to a placebo or to existing therapies. While most of our trials compare single medications, others compare combinations of different medications or various dosage levels.

Depending on the stage of a drug or treatment development, trials usually start as small pilot studies. As safety and effectiveness data are established, trials can become much larger, sometimes involving many thousands of volunteers at different sites.

Step One

RECRUITING & ENROLLING VOLUNTEERS

Our first job is to recruit and qualify volunteers to join a study and to retain them for the entire length of the trial (usually several months, but sometimes longer). 

We carefully screen all volunteers to make sure they are generally healthy, and/or have the characteristics determined as necessary by the study sponsor.

Step Two

CONDUCTING THE TRIAL

Each trial is conducted according to precise methods called protocols, as determined by the trial’s sponsor. Since many trials involve conducting studies in different sites at the same time, a protocol ensures that studies at multiple sites are consistently performed in exactly the same way.

Step Three

COLLECTING & ANALYZING RESULTS

We collect detailed medical information on the changes volunteers experience while using a medication or treatment. We verify the information for accuracy and then report it to the trial sponsor. We only report medical information (e.g., blood pressure, lab values, etc.) for each volunteer; never personally identifying information such as name, address, etc.

We carefully measure the safety of investigational medications or treatments. By regularly and thoroughly monitoring our study participants, we keep a very close watch for any unusual or unexpected side effects that may arise during the trial.

Once the sponsor has gathered the trial information from all sites, the data is compiled and thoroughly analyzed for submission to the FDA for approval. Any side effects, even minor ones, are recorded and analyzed. 

Reaching Patients

Our patient concierge service provides personalized support to patients, helping them with visit reminders, transportation coordination, medication reminders and other tasks that challenge participation in clinical research. We offer 100% recruitment without patient abandonment.