Why Oncquvia

  • We ensure that the study is conducted at the highest standards of quality, ethics and performance
  • Maintain data’s scientific & ethical integrity
  • One size does not fit all-customized site support for resources
  • Assist investigators in day-to-day study conduct activities

Value

Quality : Timely delivery of quality data is our SOP

Time : Oncquvia team is dedicatedly working to set the high standards of quality everyday.

Cost : Oncquvia team is dedicatedly working to make the strategies for   fast recruitment, to minimize the query at sites and reduce the delivery time which help to complete the recruitment on time. This save a huge cost.

What makes us different

  • Adapt to customer needs
  • Exceed expectations
  • Jointly work with Sponsor’s/ CRO’s team
  • Systematic management of patient recruitment and retention
  • Quality Data
  • Speedy Recruitment i.e. Faster First Patient First Visit, database lock
  • Increase CR proficiency by lowering number of queries generated and quick CRF retrieval.
  • Contingency Plans
  • Human Resource Management
  • Trained & accredited staff

Our Strength

We have a database of more than 200 GCP trained doctors already engaged in doing clinical trials in various therapeutic areas.

We have more than 300 physicians in our referral network which helps our sites in timely recruitment.

Site team along with the coordinator is ICH-GCP trained and fully equipped to strategize activities from the word “Go”.

We have a cumulative database of more than 10,000 critically ill patients which are also trial naïve. This has helped us in strategizing recruitment and pacing recruitment efforts evenly to attain smooth workflow. This has also helped us in supporting high recruiting requests.

We have well qualified science graduate, trained and dedicated study coordinators at each site for smooth conduct of clinical trial.

Local clinical Trial Manager in every city to oversee the work of CRCs, help in site set-up  and  do the start up activities.