Clinical Research Solution and Bioanalytical Team

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

VeedaCR Most Trusted CROs in India

Our value system along with a commitment for innovation, perfection and quality has given us the recognition of one of the safest and most trusted in for & .

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We are one of the leading in , delivering a range of extensive services for , Inhalation, Suppository, Glucose Clamp, and more.

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Govt to Bring All Medical Devices Under CDSCO Lens to Improve Safety & Quality

The government plans to bring all , including implants and contraceptives, under the lens of the Central and Standard Control Organisation so as to improve their safety and quality.

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FDA Finalizes Guidance Reviews for Cancer Clinical Trials

The 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.

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FDA Releases Updated RTA Checklist

The guidance replaces the 30 October 2017 draft guidance of the same name and describes the administrative steps will take to either Refuse to Accept (RTA) or file a request for an evaluation of automatic class III designation (De Novo request).

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General Drug Controller of India

All approvals from the Controller General of India (DCGI) will go completely online to ensure to global as well as domestic players, according to V G Somani, DCGI.

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to Ship With QR Codes

In an attempt to ensure authenticity, every active pharmaceutical ingredient (API) manufactured or imported in the country will soon bear a quick response or QR code on its label to facilitate tracking.

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Roundup: India Forms Technical Advisory Group to Help

Australia’s Goods Administration (TGA) has revealed that parts of the industry objected strongly to its recently adopted standard for tablets and .

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The Union health ministry has constituted a committee which will advise the Central Standard Control (CDSCO) regarding the strengthening of medical devices regulations in the country and also examine issues relating to their implementation.

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