Who We Are What We Do Benefits Specialties Contact

Site Management Organization

01 .

IPIC SMO
Clinical
Research

A multidisciplinary team of healthcare professionals committed to operational excellence and regulatory quality in every clinical study.

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Project Management

02 .

Managing
clinical
research

Comprehensive support for investigators and sites — from first protocol contact through final study close-out.

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Quality Standards

03 .

Driving
study
excellence

Upholding the highest quality standards across every clinical trial activity — standardizing processes and supporting every stakeholder.

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10+Years active
16Therapeutic areas
GCPCertified team
CBACórdoba, Arg.
Who we are

An SMO built for clinical research excellence

10+

Years active

16

Therapeutic areas

GCP

Certified team

IPIC SMO is a Site Management Organization formed by healthcare professionals with deep expertise in clinical research. We deliver specialized management services to Research Sites, the Pharmaceutical Industry, and Contract Research Organizations (CROs) — optimizing administrative, regulatory, and legal workflows.


Our mission: facilitate the development of clinical studies under the most rigorous quality standards, standardizing procedures and providing personalized support to principal investigators, sites, and sponsors at every step.

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Services

What we do at IPIC SMO

End-to-end management of clinical research projects — from protocol reception through study completion.

/ 01 .

Promoting healthcare facilities that wish to develop as Research Sites.

/ 02 .

Drafting and implementing site-specific Standard Operating Procedures (SOPs).

/ 03 .

Designing a tailored recruitment plan for each study protocol.

/ 04 .

Training in GCP, local regulations, and ALCOA+ for all delegated study staff.

/ 05 .

Regulatory affairs: preparation and submission to Ethics Committees and local regulatory bodies.

/ 06 .

Full coordination support throughout the entire study lifecycle.

/ 07 .

Data entry services: CRF completion, query resolution, and data management.

/ 08 .

Administrative management: invoicing, collections, and fee disbursement.

/ 09 .

Contract and budget negotiation with Sponsors and/or CROs.

/ 10 .

On-site support during monitoring visits, audits, and regulatory inspections.

Our pillars

Why choose IPIC SMO?

Five core principles that drive every decision and every process.

01

Site Development

02

Quality

03

Profitability

04

Recruitment

05

Coordination

For Sponsors & CROs

Site Network.
Quality Data.

Partnering with IPIC SMO gives you access to a growing network of public and private sites in Córdoba Province — with trained, committed investigators ready to meet sponsor expectations from day one.

We are committed to shortening and optimizing timelines for:

Pre-feasibility and feasibility responses
Regulatory package submission & initial approvals
Study Start-Up
Contract negotiation
CRF completion and query resolution
Response to Sponsor / CRO requests

We continuously train investigators in ALCOA+ principles — guaranteeing data quality and integrity throughout the entire study.

Specialties

Areas of Interest

Vaccines Oncology Hematology Cardiology Infectious Diseases Immunology Nephrology Pediatrics Endocrinology Rheumatology Neurology Gastroenterology Ophthalmology Dermatology Diabetes Diagnostic Imaging
Contact

Let's talk

Interested in partnering with IPIC SMO? Send us a message and our team will respond promptly.

Email contacto@iic-cordoba.org
LinkedIn linkedin.com/company/ipic-smo
Location Province of Córdoba, Argentina