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, MAPA, Controllab, Controlados Portaria 344/98, INMETRO (Medical Devices) – Recognized by Cgcre for BPL under number 0086. The scope can be consulted directly on INMETRO’s website.
  • LabMass
    REBLAS (drugs, oncology, cannabis), Portaria 344/98, MAPA
  • Lychnoflora
    REBLAS, MAPA, 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
 
PreviousNext

Our services

Link to: Analytical and bioanalytical services

Analytical

Services

Link to: Clinical trials

BA/BE

& 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

This field is for validation purposes and should be left unchanged.

Hello! How can we help you?

Name(Required)
Consent(Required)

By contacting QIMA Life Sciences you agree to our privacy policy and terms and conditions.