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Press Release
28th November 2005
Veeda Clinical Research – unleashing the power of India
The 15 billion dollar world of Clinical Research has a major new
player in its fastest growing sector, that of phase I clinical
trials. Veeda Clinical Research, known as Veeda CR, brings together
the highly respected UK CRO Phase 1 CTU, ClinSearch Labs Pvt. Ltd.
of Ahmedabad and Triphasic Clinical Trials Laboratories a Plymouth,
UK based, GLP accredited laboratory.
Veeda CR can count many of the world’s top ten Pharmaceutical
Companies as clients and sees huge potential in unleashing the
synergies of its Indian - European collaboration onto a global
market place. Veeda CR’s revenue in India currently stands at 32
crores and is expected to double over the next 12 months.
“Veeda CR represents the ideal bridge between cultures –
combining vast experience and expertise in handling the most
technically complex trials to the most stringent regulatory
standards with the massive technical, data management and volunteer
capability of the Indian subcontinent” said Director Mr. Apurva
Shah.
Veeda CR sees its key attribute as its uncompromising commitment to
quality and it will use the recognised expertise of its European
personnel to help train its research professionals in India. This
will be achieved by a two way traffic between continents with
research professionals from India undergoing intensive training in
the UK and Western project management skills following European
research projects into India.
Dr Kiran Marthak, a Director of Veeda CR, is delighted to have
joined the Veeda CR at this exciting juncture. Dr Marthak is a
pioneer of clinical research activities in India and brings to Veeda
CR experience of working with pharmaceutical majors such as Novartis,
German Remedies, Pfizer, and Ranbaxy.
Dr Marthak said “We have managed to combine the best of a top 5
Early Clinical Development Unit in the UK, with all the advantages
of a vibrant new unit on the Indian subcontinent, with both Units
operating to exactly the same stringent standards set by
international regulatory authorities”
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