QIMA Life Sciences Brazil

Your Brazilian one-stop-shop CRO for your princeps and generics developments.

About QIMA Life Sciences Brazil

Laboratories and clinical services supporting R&D and quality-control studies for the pharmaceutical, veterinary, cosmetics, and medical-device industries.

Brazilian companies under the QIMA Life Sciences umbrella:

  • 20+ years’ experience
  • 450 FTEs in 5 locations
  • 7000+ m² of Labs

End-to-End Services: From Discovery to Clinical

QIMA Life Sciences Brazil supports you from Early Discovery to Market and Post Market Steps.

Quality & accreditations

  • Apex
    REBLAS (drugs & cannabis), MAPA, Controllab, Controlados Portaria 344/98, INMETRO (Medical Devices)
  • LabMass
    REBLAS (drugs, oncology, cannabis), Portaria 344/98, Controllab
  • Lychnoflora
    REBLAS, MAPA, Controllab, Portaria 344/98
  • ICF
    ANVISA (Brazil), ISP (Chile), ISO 17025, Audited by +20 international companies
  • CPQuali
    GCP compliance, ANVISA inspection, readiness for FDA/EMA audits, audited by national & international sponsors

Our services

Link to: Analytical and bioanalytical servicesLink to: Clinical trials

CDMO Manufacturing

& Formulation

Our Markets

Pharmaceuticals

Cosmetics

Veterinary Medicine

Medical Cannabis

Medical Devices

Chemicals

Why choose QIMA Life Sciences end-to-end CRO in Brazil?

Description

Integrated End-to-End Services

  • State‑of‑the‑art analytical laboratories with capabilities for complex analyses
  • Seamless integration between preclinical, clinical, and analytical services
  • Process optimization for analytical and clinical workflows

Description

Collaborative Project Management

  • Transparent, agile project management with close partner engagement
  • Multidisciplinary team with advanced degrees in Pharmacy, Chemistry, Engineering, and Biology
  • Consulting and technical support in product development and regulatory compliance

Description

Commitment to Quality & Expertise

  • Delivering high‑quality solutions and reliable results
  • Deep experience across the pharmaceutical industry and academia
  • Technical and regulatory expertise to solve complex challenges (ANVISA, MAPA, FDA, EMA, ICH, USP)

Description

Efficiency & Added Value

  • Time and cost savings through streamlined processes and rapid decision‑making
  • Reliable, on‑time delivery that meets project deadlines and adapts quickly to needs
  • Training and technology transfer to build client capabilities

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