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 We Strive To Develop Innovative   Treatment Options For Patients 

Clinical Development

 

The DELTA HEALTH GROUP collaborates with other innovator companies to partner and co-develop therapeutic candidates in the clinical phase of the development process. 

Our team members have extensive clinical development experience in diverse specialties and indications, including:

  • Cardiovascular Diseases

  • Dermatology

  • Oncology

  • Endocrinology

  • Gastroenterology

  • Nephrology

  • Hematology

  • Neurology

  • Ophthalmology

  • Urology

  • Pain Management

  • CNS

  • Immunology / Autoimmune

  • Pulmonary / Respiratory

  • Psychiatry

  • Rheumatology

  • Infectious Diseases

  • Orthopaedic Surgery

 

Use of safe drugs, biologics and medical devices is critical to their pre- and post-approval therapeutic success. Over two decades of experience working directly with the US FDA and Health Canada has greatly enhanced our expertise in the areas of clinical development and drug safety.

 

With extensive experience leading to full approvals, the DELTA HEALTH GROUP offers a one-stop-shop for US FDA INDs, NDAs, 505(b)(2)s and ANDAs. 

 

In addition to the United States Food and Drug Administration (FDA) and Health Canada, the DELTA team also has experience in working with the European Medicines Agency (EMA), Ministry of Health Mexico, Argentina Administración Nacional de Medicamentos, Alimentos y Tecnología Médica (ANMAT) and the Ministry of Health Türkiye.

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To support our clinical development programs, we have partnerships with specialized pathology laboratories in the United States offering comprehensive expertise in:

 

  • Flow Cytometry - Immunophenotyping for leukemias and lymphomas

  • Cytogenics - Study of Chromosomes for various cancers

  • Fluorescent In-Situ Hybridization (FISH) - studying chromosomes with various breakpoints in different types of cancers

  • Next Generation Sequencing (Molecular Genetics) - DNA and RNA testing for various cancers

  • Digital pathology


Global Clinical Trial Investigative Sites
"Running Clinical Trials Where Patient Populations Are Located" 

Our Clinical Trial Investigative Sites

 

The DELTA HEALTH GROUP operates a global network of dedicated and strategically located clinical trial investigative sites in the United States, Canada and the Asian continent

 

  • With advanced infrastructure and world-class medical facilities, these high-performance international investigative sites include partner Phase 1 Clinics and dedicated Phase 2 and pivotal Phase 3 medical centers and hospitals that are focused on conducting US FDA drug development clinical trials

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  • Based on the maxim.....Experience.....Integrity.....Quality, we believe in running clinical trials where the patient populations are located. This includes running new drug development trials at our premier sites in Asia by reaching out to diverse, treatment naive patient populations

  • DELTA HEALTH has long-term exclusivity agreements with prominent teaching hospitals and clinics in Asia to operate and manage state-of-the-art, multi-specialty, clinical investigative sites having extensive experience in conducting drug development clinical trials according to ICH Good Clinical Practice Guidelines. Covering a multi-million, diverse ethnic catchment area population, these clinical facilities have preferred access to a fast growing and highly compliant, local clinical trial subject populace ​

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  • The clinical trial facilities in Asia are directly mentored and managed by the DELTA HEALTH team members stationed locally on the ground. These Delta Specialists have in-depth knowledge and hands-on experience with the direct management of successful US FDA clinical trials and investigative sites

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  • With 60% - 70% drug development clinical trials resulting in failure due to patient recruitment inability or delays and another significant number falling short of meeting study objectives, the DELTA HEALTH operated investigative sites in Asia work diligently with key stakeholders to take challenges head-on and make smart decisions to overcome common obstacles seamlessly  

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  • Speedy start-up of clinical trials, enrollment of compliant patients and collection of clean, audit ready data is ensured by the US FDA seasoned and vetted DELTA HEALTH team

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  • Supported by AI optimization tools and advanced Data Management systems, the operational excellence of our EMR and EDC savvy teams give us the capability to run clinical trials at multiple sites simultaneously   

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  • Modern, internationally certified clinical laboratories and diagnostic facilities with in-house CT scans and MRIs provide dedicated support throughout the duration of ongoing clinical trials 

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  • Bereft the red-tapism and overheads of industry giants, engaging the DELTA HEALTH clinical trial sites will dramatically cut study timelines to accelerate the successful execution of partner clinical development programs

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Collaborate with the DELTA HEALTH GROUP to expand your existing site network and partner with us to conduct your studies at our premier international clinical trial investigative sites.

Smiling doctor woman holding earth globe

Fast-Track Regulatory and IRB Approval

 

Our streamlined, one-window-operation for the local Regulatory and IRB approval process in Asia goes through a fast turnaround to facilitate expedited start-up of clinical trials.   ​​

 

© 2025 DELTA HEALTH GROUP (Including Global Subsidiaries and Affiliates Collectively).
ALL RIGHTS RESERVED   

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