Management of Trial at Site

Oncquvia understands this & thus provides dedicated, full time and experienced CRCs to prioritize the work appropriately and be able to serve every trial related activity at the site.

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Management of Trial at Site

Oncquvia understands this & thus provides dedicated, full time and experienced CRCs to prioritize the work appropriately and be able to serve every trial related activity at the site.

View More

Monitoring Services

We have a team of well-trained monitors having experience in Phase I and late Phase studies in various therapeutic areas.

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Monitoring Services

We have a team of well-trained monitors having experience in Phase I and late Phase studies in various therapeutic areas.

View More

Independent Quality Assurance

Our Audit team comprises of well experienced QA Auditors and GCP trained Medicos

View More

Independent Quality Assurance

Our Audit team comprises of well experienced QA Auditors and GCP trained Medicos

View More
ABOUT US

Oncquvia Clinical Research

Oncquvia Clinical Research, is a Site Management Organization based in Varanasi & operational since 2021.

Oncquvia partners with the pharmaceutical, biotechnology, and medical device companies for a successful outcome in their drug development endeavors.

Oncquvia identifies and presents potential investigative sites and medicos across all therapeutic areas and has a vast database of them ready for your disposal.

Our dedicated team committed to the advancement of development of drugs while safeguarding the rights and safety of research subjects.

OUR FOCUS

Our Strategy

  • Identify highly qualified, enthusiastic, experienced & competent investigators in different therapeutic areas.
  • Speed-up site identification, qualification, initiation, budget/ contractual negotiations and reduce start-up time.
  • Facilitate Sponsor’s/ CRO’s access to a commercial Independent Ethics Committee (IEC) qualified to review protocols, provide feedback, approvals & requests for modification.
How we help Sponsors or CROs?

Solutions

We provide unparalleled service with our finest resource. Our customized service ensures that we satisfy your specific and unique needs.

  • Identify Potential Investigators
  • Site Evaluation & continually develop new investigative sites
  • Establish & maintain Regulatory compliance at clinical sites
  • Train Study team
  • Establish effective communication with Ethics Committee
  • Not only in metropolitan but also in second tier cities

This gives an opportunity to identify experienced investigators with excellent site infrastructure and naïve patient pool.

We Develop our capabilities in

Our Capabilities

  • Medical & Operational Assessment (Top-line Feasibility)
  • Detailed Feasibility Studies
  • Site Identification, Evaluation, Selection and Training
  • Country Regulatory and Ethics submission
  • Independent Site Monitoring
  • Independent Vendor Monitoring
  • Independent Audits – DCG(I) and US-FDA styles
  • Medical Monitoring
  • Medical Writing
  • Pharmacovigilance and Safety Reporting
  • Vocational training for aspiring CRAs, CRCs and Investigators
What we do

Our Services

01.

Management of Trial at Site

We strongly believe Clinical Research Coordinators play a vital role in bringing success by assisting the investigators in the preparation and conduct of the trials.

02.

Monitoring Services

We have a team of well-trained monitors having experience in Phase I and late Phase studies in various therapeutic areas.

03.

Services during trial

  • Assist in ICF process, screening and enrollment
  • Coordinate subject follow up visits
04.

Independent Quality Assurance/GCP Auditing

Our Audit team comprises of well experienced QA Auditors and GCP trained Medicos.

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Testimonials

What They Say About Us

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