ADI being awarded with "AWARD OF EXCELLENCE" by State Government and Software Technology Parks of India (STPI) for its best performance in 2008-09 in IT Enabled Service.
Before each new drug/ device/ treatment launch into the market, it has to pass through a lengthy research and approval process which takes around 12- 16 years. Clinical trials are conducted to allow safety and efficacy data to be collected for new drugs or devices. The whole process from the lab to an established form of treatment is called as clinical research and this is where several of professionals are required. The trials can only take place once satisfactory information has been gathered on the quality of the non-clinical safety, and Health Authority/Ethics Committee approval is granted in the country where the trial is taking place.
ADI Group was incorporated in 2004 who on first step acquired a 4-year-old medical transcription company.
ADI is headquartered at Mohali (Chandigarh), India. We also have global presence in USA and UK.
ADI Group has strength of 140 personnel including 25 Doctors, 3 Ph.D., 12 MBA, 10 Biomedical Engineers, 15 Software Engineers, 25 Postgraduate and 30 Graduates.
Medical writing is an art of preparing and designing clinical content for a Professional journal or a Health care website or an Equipment Manual that attracts attention and ensures loyalty of the web surfer/ End user/ Medical Professional. As a promoter or professional engaged with Website/ Equipment/ Journal we also feel that our content will attract others but it requires enormous effort to have this by ourselves.
To achieve this we require skilled medical writing experts equipped with formatting, scientific data collection, analysis of other products in the market, aesthetics techniques. The Professional Medical writing team at ADI has the expertise to do this and offer you tailor made solutions for your products.
ADI CRO is an emerging clinical research organization (CRO) dedicated to provide complete range of early to late stage clinical development services. Our professional expertise includes: Clinical data management services which include maintenance of CSR, CRF and Site Initiation Monitoring and Closeout database design etc. Also we have experts in Biostatistics and Statistical Programming that include all the statistical calculation work for undergoing clinical studies, Medical and Scientific Writing and Pharmacovigilance. ADI CRO have also developed in-house standard operating procedures to fulfill ICH and GCP recommendations.
ADI render its services to overseas and offshore client.
ADI CRO are dedicated to provide total program development services. Our team of strong clinical and therapeutic area expert & professionals engaged in clinical services, data services and post-approval services.
You can know more about ADI through the presentation.
It is very easy, fill in our enquiry form or send us your requirements at info@adicro.com Our experts will contact you.
We will need to know what kind of service you are interested in and the nature of your project.
Yes. You will own the copyrights for all the material written for your project. We will also maintain strict confidentiality and never share any of the content with any other clients.
ADI has a standard Non-Disclosure Agreement that we are willing to adapt to your specifications/requirements. We can consider your NDA with the consent of our legal department.
We can work with deadlines. But we can estimate the exact time required better once we understand the finer details of your project.
Yes, many times and we welcome site audits by potential clients.
Yes, we have SOPs in place for all our processes.
If you have any more questions regarding our services, please contact us. Our team will be happy to answer your questions.