Identifying the Right Investigators and Patients for your Study – Mini Podcast Biosimilar Development Capabilities – Watch Now Vaccine Development Capabilities - Brochure Check out our latest Validated PK & ADA Methods List Read about Veeda's partnership with Ahammune Biosciences for first in human studies Check out our Assay List (Method Library)

Phase II - Phase IV Clinical Trial Management

Phase II - Phase IV Clinical Trial Management

Veeda’s full-service clinical trials operations support our clients with study feasibility, pre-site qualification, initiation, patient recruitment services, site management services, and study monitoring (including Central Monitoring, Remote Monitoring & on-site monitoring) to ensure patient safety. Our well-trained and highly competent Project Managers, Senior Clinical Research Associates, Clinical Research Associates, and Clinical Trial Assistants have years of experience in various therapeutic areas and have worked with more than 900 clinical investigators across a wide range of therapeutic areas including Oncology, Infectious Diseases, CNS, Dermatology, Respiratory, Endocrinology, Haematology, Immunology.

Combined Team Experience in >300 clinical Trials
10+ Therapeutic Areas
250+ Sites
900+ Investigators Database

Veeda helps Biopharmaceutical & Pharmaceutical sponsors accelerate Clinical Trials with faster Site Selection and Patient Recruitment for the following Indications

POC Study
    • HIV
    • Covid -19 Vaccine (Phase I/II)
    • Colon or Pancreatic Cancer
Phase II/III
    • Relapsed Advanced Tumors and classical Hodgkin Lymphoma (cHL)
    • Asthma
    • COPD
    • Human head lice infestation
Clinical End Point
    • Open angle Glaucoma
    • Chronic idiopathic constipation
Patient PK
    • Multiple Myeloma
    • Postmenopausal Osteoporosis
    • Schizophrenia
    • Advanced Prostate Cancer
    • Ovarian Cancer
    • Breast Cancer
    • Iron Deficiency Anemia
    • Renal Carcinoma
    • Small Cell Lung Cancer
    • Rheumatoid Arthritis

Solutions That Are Flexible & Tailored to your Clinical Trial Needs

Medical Writing

Our Medical writing team offers expert support to help our sponsors communicate clinical trial information to patients, sites, and regulatory authorities. We can assist our clients with the services like Protocol development & amendments, Informed Consent Forms, Case Report Form preparation, Clinical study reports, etc

Our Recruitment & Retention Strategies

Our Effective patient recruitment strategies, Pre-identification of patients as per the study, counselling patients ensuring willingness for trial participation, help to maintain a healthy pool of subjects, and participant retention is paramount to conducting successful studies

Project Management

Our experienced project managers with proven expertise across the full development continuum provide direction to our project management team to successfully manage the triple constraints of the project: Cost, Time & Resources

Site Management

Our skilled and well-trained clinical research associates (CRAs) ensure the highest quality review of data and effective interaction with study sites, which helps us to successfully ensure site selection & Monitoring according to the protocol requirements

Regulatory Guidance

At Veeda, we have a dedicated team that focuses on the client’s regulatory requirements, which need to be fulfilled before a clinical study is initiated. We work together to assist our sponsors with complex regulatory issues, pathways, and regular tracking of the application status along with changing requirements to ensure study-related approvals are in place, promptly

Safety Database and Pharmacovigilance

We aim to ensure patient safety and adhere to the regulations. We can provide case processing, safety reporting, and Medical support services to help our sponsors meet the patient safety criteria as per their study requirements

40 +

Completed Patient Studies

Successfully completed

23 USFDA & 3 EMA

inspections across sites without 483 observations

4000 +

Patients Enrolled

16 +

Ongoing Studies (Including Phase I/II/IIa studies, Patient PK & Clinical Endpoint


  • Tailored solutions for adaptable study design and execution
  • Agile approach for seamless adaptation to changing circumstances

Quality & Compliance

  • Robust systems ensuring data integrity and regulatory compliance
  • Regular audits for adherence to ethical and regulatory standards


  • Meticulous planning for streamlined study operations and execution
  • Advanced technologies optimizing processes for efficient study completion