Streamline your clinical research with our end-to-end dossier services. Our expertise includes:

Concept Development for Clinical Research Design

Transforming innovative ideas into actionable research studies is our forte. We work closely with Investigators and Sponsors to create comprehensive clinical research designs. Our team ensures that the concepts align with the study objectives while adhering to regulatory and ethical standards, paving the way for impactful results.

Clinical Study Protocol

We develop detailed, well-structured clinical study protocols that outline study objectives, methodology, and endpoints, ensuring clarity and regulatory compliance.

Informed Consent Forms

To support patient-centric research, we create informed consent forms in both English and vernacular languages. We ensure these forms are clear, concise, and ethically sound, enhancing patient understanding.

Back Translation Services

Accuracy in translation is critical for patient safety and regulatory compliance. Our back translation services verify that informed consent forms maintain their original meaning, regardless of language.

Case Record Forms (CRF)

We design CRFs tailored to your study requirements, ensuring comprehensive and precise data capture for reliable study outcomes.

Patient-Related Questionnaires

Engaging patients is vital for quality research data. We create customized, easy-to-understand questionnaires that capture relevant insights while ensuring a positive patient experience.

Patient Information Leaflet

Educating participants about the study is a key part of our services. We design patient information leaflets that clearly explain the purpose, process, and benefits of the study, empowering participants to make informed decisions.