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