Welcome to PhaseON Clinical Research
In this ‘ever challenging and rapidly changing environment’, you need a partner that is flexible and responsive – one that delivers complete trust and quality. Through our full-service capability and experienced team located in INDIA, we are ready to meet the challenges of conducting clinical trials in India. That’s PhaseON – ready to help right where you need us.
PhaseON Clinical Research is a leading, full service, Global Contract Research Organization with extensive experience in the management of Phase II-IV Clinical Trials across a broad range of Therapeutic Areas, Patient PK Studies, Clinical Data Management with BioMetric services, Independent Third Party Monitoring / Audits and Contract Staffing Solutions with a commitment to operational excellence using our proven and trusted process.
Delivering Quality Drug Development Process
Our specialized experience is focused on the value that these regions bring to our customers in terms of quality clinical programs conducted by some of the most experienced clinical staff in India.
At PhaseON, we focus on doing what we do best: on helping highly innovative biopharmaceutical and medical device companies bring their life-changing developments from initial strategy through clinical development to successful regulatory submissions. We at PhaseON also specialize on clinical development of Nutraceuticals’ and Ayurvedic products for evidence based studies.
Our Health Care Solutions
Generic Drug Development
Generic drug development involves Patient PK studies and independent monitoring of BA/BE studies, ensuring compliance and accuracy for generic pharmaceutical companies conducting clinical research.
Independent Monitoring
We provide expert representation for Sponsors in India, offering independent monitoring and audits for BA/BE studies, covering both in-process and retrospective evaluations across clinical and bioanalytical phases.
Quality Assurance
Our highly experienced Quality Assurance personnel ensure compliance, maintaining high-quality standards for all clinical studies conducted at PhaseON to guarantee reliable and efficient drug development processes.
Regulatory Affairs
Understanding regulatory importance in drug development, our dedicated team liaises with agencies, ensuring smooth approvals and accurate clinical trial submissions for pharmaceutical research success.
Investigator identification
Our feasibility expertise, combined with an investigator network in India enables precise site selection while deploying PhaseON-trained CRCs to support study teams onsite.
Drug Storage & Distribution
Drug storage, distribution, and logistics are critical for clinical study success. At PhaseON, we provide proven solutions ensuring efficiency, reliability, and seamless management of pharmaceutical research needs.
The PhaseON Advantage
- Huge database of more than 1000 ICH-GCP trained Investigators and sites in India & Sub continent
- Highly Experienced teams having worked in India & Sub continent; Germany to offer that differentiator of Local Expertise in these regions
- Experienced teams and Project Management Capabilities to offer value added service and identify the critical areas for risk mitigation and timely execution
- Knowledge based approach having a unique combination of in-house expertise and on board KOLs across therapeutic areas
- An Audit Ready Team - Team experienced in successfully facing various Regulatory and Sponsor / Sponsor initiated independent audits
- Strong Quality Assurance backbone supported by robust in-house SOPs
- Team having a proven track record of timely execution of projects and highest level of compliance resulting in customer satisfaction
- System driven execution approach