Clinical Trial Management System
#ClinicalStudy teams are increasingly being challenged due to delays caused by unsecured systems, manual data re-entry, redundant workflows, and information. Veeda’s #ClinicalTrialManagement System provides the ability to plan and manage all of your #clinicaltrials efficiently.
www.veedacr.com/organization/achievement/

We place a firm emphasis on following our value system to deliver excellence in Clinical Trials. Subject safety being of primary importance, we ensure that the studies are conducted according to strict scientific and ethical principles. This has helped us establish ourselves as one of the most trusted CROs in India.www.veedacr.com/services/bio-analytical/

We operate under a robust #QualityManagement System that is designed to ensure that the services that we offer are compliant to all applicable #regulatory and quality standards, guidelines and laws.For business inquiries, write to us at info@veedacr.com or visit www.veedacr.com/organization/

Delivering Excellence in Bioanalytical ServicesOur in-house expertise and access to sophisticated and modern infrastructure enables rapid turnaround times for bioanalytical services.For business inquiries visit www.veedacr.com

Best CRO Services in IndiaWe have a sharp focus on delivering streamlined and comprehensive quality solutions to help pharmaceutical companies bring new medications to patients using a more collaborative and efficient approach.For business inquiries, write to us at info@veedacr.com or visit www.veedacr.com

Clinical Trial DevelopmentWe offer quality solutions from clinical development to post regulatory submission. Our expertise spans across multiple therapeutic areas, phases of clinical trials, special areas such as Inhalation, Glucose Clamps, Biosimilars etc.For business inquiries, write to us at info@veedacr.com or visit www.veedacr.com

Inhalation StudiesOur experienced staff, world-class infrastructure and extensive training process for volunteers have helped us in conducting 22 successful inhalation studies till date.For business enquiries, write to us at info@veedacr.com

Veeda CR Best Quality Clinical TrialsWith our state-of-the-art infrastructure, we have completed more than 2700 Clinical Studies and over 550 standalone bioanalytical studies so far thus becoming the safest and the most competent partner for the leading pharmaceutical brands across the world.For business enquiries, write to us at info@veedacr.com

Researchers Testing Drug That Reduces Breast Cancer by 50 PercentA new drug has been found to reduce the risk of cancer reoccurring by 50 percent and a Richmond hospital is behind a major medical breakthrough for breast cancer patients. It brings new hope to patients like 42-year-old Katharine Brookeman.

Conducted Complex StudiesThe challenge of focusing on the best study design for ‘very complex modern clinical trials’ is particularly concerning for the industry. We at Veeda, are committed to improving the quality and accuracy of trials by simplifying the process.

Strategic Volunteer RecruitmentWith an effective backup team and adhering to strong volunteer ethics, we offer timely solutions to practical difficulties in volunteer recruitment to accomplish all your clinical research needs.For business enquiries, write to us at info@veedacr.com

We are known for providing quality #clinicalresearch solution and our #bioanalytical team is recognized for developing bioanalytical methods for conducting Immunogenicity studies, Complex analysis for Vitamins, Steroids and Hormones and Elemental Bioanalysis.

VeedaCR Most Trusted CROs in IndiaOur value system along with a commitment for innovation, perfection and quality has given us the recognition of one of the safest and most trusted CROs in India for BA BE studies & Clinical Trials.For business enquiries, write to us at info@veedacr.com

Quality Clinical Research SolutionWe are one of the leading CROs in India, delivering a range of extensive clinical research services for BA BE studies, Inhalation, Suppository, Glucose Clamp, clinical trials and more.

Challenges and Opportunities for Indian Pharma Industry

Govt to Bring All Medical Devices Under CDSCO Lens to Improve Safety & QualityThe government plans to bring all medical devices, including implants and contraceptives, under the lens of the Central Drugs and Standard Control Organisation so as to improve their safety and quality.lnkd.in/fWCSxrt

FDA Finalizes Guidance Reviews for Cancer Clinical TrialsThe US Food and Drug Administration (FDA) on Wednesday finalized guidance on an optional streamlined submission process for determining the risk of an investigational in vitro diagnostic (IVD) in a clinical trial where an investigational IVD is being co-developed with an oncology investigational drug.FDA Finalizes Guidance on Streamlined IVD Reviews for Cancer Clinical TrialsRead More: lnkd.in/fHUKHvVhttps://bit.ly/35XGStw

FDA Releases Updated RTA ChecklistThe guidance replaces the 30 October 2017 draft guidance of the same name and describes the administrative steps FDA will take to either Refuse to Accept (RTA) or file a request for an evaluation of automatic class III designation (De Novo request).Read More: bit.ly/2pe7Qws

Recent Traction In FDA's Development Of The 503A And 503B Bulks Lists.Read More: lnkd.in/fsMQp8Nhttps://bit.ly/2lEzfG9