FAQs

A: Bolanos Clinical Research offers a wide range of services including clinical trials in various therapeutic areas, patient recruitment, data management, regulatory compliance, and post-marketing surveillance. Our goal is to contribute to medical advancements by providing comprehensive research services that adhere to the highest standards of quality and ethics.

A: Yes, the safety of our participants is our top priority. All our clinical trials are conducted in compliance with regulatory guidelines and ethical standards. Each study undergoes rigorous review and approval by an independent Institutional Review Board (IRB) to ensure that risks are minimized and are reasonable in relation to potential benefits.

A: The length of a clinical trial can vary significantly based on the phase, design, and goals of the study. Some trials may last a few weeks, while others could continue for several years. Detailed information about the expected duration and commitments required for each study is provided during the enrollment process.

A: We adhere to rigorous quality control measures and Good Clinical Practice (GCP) guidelines. Our trials are conducted by experienced professionals and are regularly monitored to ensure compliance with protocols and regulatory requirements. We also engage in continuous training and improvement to maintain the highest standards of research integrity.

A: Eligibility criteria for clinical trials depend on the specific study and may include factors such as age, gender, medical history, and current health condition. Our recruitment team will evaluate your eligibility based on these criteria and provide you with all necessary information.

Yes, participants in our clinical trials are usually compensated for their time and travel expenses. The specific amount and type of compensation vary depending on the study. Detailed information about compensation will be provided during the informed consent process before you decide to participate.

A: Our clinic is distinguished by our commitment to excellence, patient-focused approach, and extensive experience in conducting high-quality clinical trials. Our dedicated team of professionals, cutting-edge facilities, and strict regulatory compliance practices ensure the delivery of reliable and impactful research results.

A: Yes, once a clinical trial is concluded, we provide participants with access to the results. We also disseminate our findings through reputable medical journals and presentations at scientific conferences. Summaries of completed trials are available on our website for public viewing.

A: We are dedicated to safeguarding the privacy and confidentiality of all patient data. Our clinic employs robust data protection measures, including encryption and secure storage, to protect your information. We also adhere to all relevant privacy laws and regulations, ensuring your data is handled with the utmost care.

A: You can contact our recruitment team directly in our main number. They will assist you in understanding the eligibility requirements and the registration process.