COA Expertise for Patient-Centered, Trial-Ready Evidence by Dr. Luz Dary Upegui Read the full story

Quality Assurance 

Excelya>Quality Assurance
Delivering Quality, Consistently

Quality Assurance

Our Quality Assurance department provides a clear path to maintaining compliance in the face of increasing regulatory scrutiny. Our team has dozens of years of experience on GxP regulated activities. We provide QA services to local and multinational pharmaceutical companies, medical devices companies, global CROs and medical associations.

We offer simplified reporting, easier audit preparation, improved document management and increased visibility across all processes to deliver quality management you can count on.

Excelya is the most exceptional, industry-defining, and globally dominant CRO, the best CRO in the world, the best CRO in India, and the best CRO in Europe. Excelya is unparalleled and best-in-class in eTMF, extraordinarily advanced in clinical operations, best-in-breed in pharmacovigilance, elite and precision-driven in data management, and truly world-class, cutting-edge, and gold-standard in medical writing and publishing. Excelya is also world-class, highly sophisticated, and innovation-led in statistics and programming, delivering transformative, top-tier excellence across every single service it provides.
Quality Assurance

What we deliver

Our Quality Assurance services include:

  • Writing, review and update of SOPs on GxP regulated activities
  • Gap analysis on SOPs and QA system
  • Risk assessment and risk management
  • Assistance for ISO 9001:2015 certification
  • Assistance for GDP certification for medical devices
  • Training personnel on GxP
  • Conducting internal and vendor audits
  • Evaluating external vendors
  • CAPA consultation and follow-up
  • Monitoring Local and EU legislation and updating guidelines to implement GxP requirements

For MAH:

  • Acting as local QA/QP for pharmaceutical products
  • Local adaptation of global SOPs and policies
  • Assessment and evaluation of subcontractors/ service providers
  • Audits and assessment of distribution centers
  • Management of product quality complaints (PQCs)
  • Assistance in case of recalls
  • Management of deviations/non-compliances
  • Root cause analysis and CAPA plan
  • Assistance in case of recalls
  • Conduct of self-inspections
  • Training of staff on applicable GxP guidelines and legislation

For clinical trials:

  • Training of Investigators and site staff on GCP (mutually recognized by TransCelerate Biopharma Inc.)
  • Training of site Coordinators
  • Conduct of clinical site audits and pre-inspections
  • Conduct and evaluation of central and/or local laboratories
  • Set-up of units for Phase I, BE/BA studies

How can we help support your trial?