ISP regulatory management
We prepare, submit and monitor health-authority procedures for regulated products.
HEALTH REGULATION · QUALITY · IMPLEMENTATION
Consulting and regulatory management for pharmaceutical, cosmetic, food, medical-device and disinfectant businesses operating in or entering Chile.
30+years of combined experience
2020year founded
ISP + SEREMIintegrated health-authority support
EXPERIENCE THAT GETS INVOLVED
Our background in operations, distribution, retail and work with oversight bodies helps us anticipate requirements, organize evidence and support each implementation until it becomes a working business capability.
Read our story ↗SERVICES
We organize the work around the authority, product and commercial objective of each business.
We prepare, submit and monitor health-authority procedures for regulated products.
We support the sanitary and commercial authorization of operations, food and supplements.
We turn technical requirements into procedures that teams can apply and maintain.
We support local and international suppliers that need an experienced counterpart in Chile.

HOW WE WORK
We review the product, operation and objective to identify the applicable route.
We organize the evidence, identify gaps and define owners and timing.
We manage the process and work with the team to apply the requirements.
We respond to observations and maintain visibility over the next milestones.
TECHNICAL LEADERSHIP
CEO & Founder · Pharmaceutical Chemist
Her background combines operational management, logistics, distribution, retail and quality-system auditing. That broad view connects health requirements with the way a business actually operates.

EXPERIENCE WITH REAL ORGANIZATIONS












Logos shown as references to experience reported by Weitzel Business Group.
REGULATORY CONTEXT
Chile's ISP has begun a gradual SAFIS rollout to consolidate authorizations and inspections historically handled in platforms such as GICONA.
Read overview ↗A strong filing begins with complete technical and legal information aligned with the product's classification, use and risk condition.
Read overview ↗Law 21,719 takes effect on December 1, 2026 and raises the standards for processing and protecting personal data.
Read overview ↗LET'S TALK
We will review your context and propose an appropriate next step.