Allucent

Small and mid-sized biotech companies have distinct development challenges from therapeutic innovations through the clinical process to approval. Allucent offers regulatory consulting, product development, clinical pharmacology, and clinical research solutions designed to support these specialized needs.

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Locations

  • Africa
  • Asia including Japan
  • Australia
  • Europe
  • North America
  • South America

Therapeutic Areas

  • Bone / Osteoporosis
  • Cardiovascular
  • Central Nervous System (CNS)
  • Dental and Oral Health
  • Dermatology
  • Diabetes
  • Endocrinology
  • Gastroenterology
  • Genetic Diseases
  • Hematology
  • Hepatology
  • Immunology
  • Infectious Disease
  • Inflammation
  • Internal Diseases
  • Metabolic Diseases
  • Musculoskeletal
  • Nephrology
  • Neurology
  • Obstetrics / Gynecology
  • Oncology
  • Ophthalmology
  • Orthopedics
  • Otolaryngology/ENT (Ear/Nose/Throat)
  • Pediatrics / Neonatology
  • Pharmacology / Toxicology
  • Psychiatry
  • Pulmonary
  • Rare Disease
  • Respiratory
  • Rheumatology
  • Surgery
  • Thrombosis
  • Urology
  • Vaccines

At Allucent we are on a mission to bring new therapies to light by addressing the distinct challenges faced by small and mid-sized biotech companies. As a global provider of comprehensive drug development solutions, we offer regulatory consulting, clinical operations, biometrics, and clinical pharmacology across various therapeutic areas. With over 30 years of experience in more than 60 countries, our individualized partnership approach provides insights and expertise to help clients successfully navigate the complexities of delivering novel treatments to patients. Allucent is the biometrics partner you can trust for collaboration and consultation on individual projects or across your entire developmental program. Our highly qualified experts work closely with your internal team, prioritizing data and statistical quality and integrity, while respecting your funding and timelines. From study design to analysis planning and regulatory submissions, our full-service data management capabilities cover the data-related requirements of all clinical trial phases as well as registrational and observational studies. Biostatistics and statistical programming proficiency are also complemented by our deep knowledge of complex indications and therapeutic areas. Working as part of your team we will prepare your therapy for the spotlight with airtight data, collected, analyzed, and delivered to the highest standards using the most current data platforms and technology. Our biometrics A-Team is ready to work side-by-side with you on: • Data Management • Clinical Programming and Data Science • Biostatistical Consulting • Biostatistics and Statistical Programming From the earliest stages of your planning process, our experienced professionals collaborate with you, providing strategic guidance and thorough, creative solutions. We’ll work in partnership with you to increase your team’s bandwidth throughout your project and support each important milestone.

Accreditations

Partners are trained on the functionality of the Coder application, process optimization, and scope of Coder services. This Accreditation teaches Partners to integrate the medical coding solution with EDC studies and administer Coder segments. Coder Accreditation is dependent on the successful completion of the Rave EDC accreditation.
Partners are trained on the functionality of the eCOA application, best practices, process optimization and the scope of eCOA services. This Accreditation teaches Partners to process patient data that has been entered by the patient themselves, or by a Clinician. Patients enter their patient data through a provisioned device or their own device after downloading the appropriate app.  Clinicians enter patient data through a provisioned device (Android or iOS). eCOA Accreditation is dependent on the successful completion of the Rave EDC Accreditation.
Partners are trained on the functionality of the electronic data capture (EDC) and clinical data management (CDM) system, process optimization exercises and scope of Medidata Rave services. This Accreditation teaches the staff to perform end user training, user and site administration, study build, reporting, outputs and amendment manager.
Partners are trained on the functionality of the RTSM Application, process optimization, best practices using RTSM, and scope of RTSM services. This Accreditation teaches Partners to conduct randomization and clinical trial supply management services (RTSM). RTSM Accreditation is dependent on the successful completion of the Rave EDC Accreditation.
Partners are trained on the functionality of the Safety Gateway application, process optimization, and scope of Safety Gateway services. This Accreditation teaches Partners to utilize the configurable EDC-to-safety-system interface to automate advanced serious adverse event (SAE) collection and E2B transmissions. Safety Gateway Accreditation is dependent on the successful completion of the Rave EDC Accreditation.
Partners are trained on the functionality of the targeted source document verification (TSDV) application, process optimization, and scope of TSDV services. This Accreditation teaches Partners to implement TSDV in line with regulatory compliance and data quality strategies. TSDV Accreditation is dependent on the successful completion of the Rave EDC Accreditation.