Now Biopharma
Now Biopharma is a clinical CRO and life‑science consultancy headquartered in Short Hills, New Jersey. The company provides clinical development and regulatory support including CRO services focused on acute care and emergency medicine, GMP and QA/GxP consulting, microbiology and laboratory consulting, regulatory strategy and submissions, patient‑registry development, and investigational product management.
Industries
Nr. of Employees
small (1-50)
Now Biopharma
Short Hills, New Jersey, United States, North America
Services
Protocol design and review, site selection and coordination, enrollment management, monitoring, and trial execution with emphasis on acute care and emergency medicine trials.
Due diligence assessments, regulatory strategy development, preparation and submission of regulatory applications, and correspondence with regulatory authorities.
Authoring controlled quality documents, designing/enhancing QA programs, and implementing governance and metrics for sustained regulatory compliance.
Advisory services to align manufacturing processes with Good Manufacturing Practice standards.
Oversight and advisory for specimen handling, clinical assays, central lab operations, and reference testing support for diagnostics and trials.
Design and implementation of patient registries, EHR data capture, stakeholder engagement, and commercialization launch planning for rare disease programs.
Protocol design and review, site selection and coordination, enrollment management, monitoring, and trial execution with emphasis on acute care and emergency medicine trials.
Due diligence assessments, regulatory strategy development, preparation and submission of regulatory applications, and correspondence with regulatory authorities.
Authoring controlled quality documents, designing/enhancing QA programs, and implementing governance and metrics for sustained regulatory compliance.
Advisory services to align manufacturing processes with Good Manufacturing Practice standards.
Oversight and advisory for specimen handling, clinical assays, central lab operations, and reference testing support for diagnostics and trials.
Design and implementation of patient registries, EHR data capture, stakeholder engagement, and commercialization launch planning for rare disease programs.
Expertise Areas
- Clinical trial management
- Emergency and acute care clinical research
- Regulatory strategy and submissions
- Quality systems and GxP compliance
Key Technologies
- Electronic health record integration
- Patient registry platforms
- Biobanking and specimen management
- Clinical laboratory assays
News & Updates
Since 2008 the organization has run more than 100 clinical research studies focused on emergency and acute care settings.
Maintains ongoing collaborations with approximately 60 emergency medicine research departments in the United States, enabling rapid site engagement for trials.
Since 2008 the organization has run more than 100 clinical research studies focused on emergency and acute care settings.
Maintains ongoing collaborations with approximately 60 emergency medicine research departments in the United States, enabling rapid site engagement for trials.