Pharmaceutical ingredient importer and distributor · ANVISA-licensed

From the world to your bench.

Brazilian importer and distributor of pharmaceutical ingredients — APIs, raw materials and excipients — serving compounding pharmacies, pharmaceutical manufacturers and distributors. Fully licensed by ANVISA, with a global network of qualified manufacturers and documented traceability from shipment to your bench.

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01 — Raw material

High-purity active ingredients

APIs, raw materials and excipients with traceable origin, for a broad range of therapeutic classes.

02 — Quality control

Testing to Brazilian Pharmacopoeia standards

Every ingredient is tested against the monographs of the Brazilian Pharmacopoeia in force, with manufacturers qualified under API Good Manufacturing Practices (RDC 654/2022).

03 — Cold chain

Monitored storage and transport

Climate-controlled area with strict temperature and humidity control, 2–8 °C pharmaceutical refrigerators and online monitoring — you track every batch from shipment to delivery.

04 — Nationwide distribution

Delivery to customers across Brazil

From import to distribution — the complete pharmaceutical ingredient chain, from origin to customer.

05 — Partnership and agility

Same-day quotes. A partner for every day.

An in-house sales team, direct WhatsApp service and complete technical documentation — CoA, SDS and analytical reports with every batch. From your first quote to routine restocking, you talk to people who know the ingredient.

Business hours, Monday to Friday (BRT) · Reply within the same business day

Who we are

Our company

Levisa was born from a conviction: Brazilian compounding pharmacies and pharmaceutical manufacturers deserve direct access to the world’s best ingredients — without intermediaries that inflate costs, without shortcuts that compromise quality. We are a new-generation importer: every batch arrives with complete documentation, referenced to the Brazilian Pharmacopoeia and issued by manufacturers qualified under API GMP (RDC 654/2022), every quote receives a traceable service protocol, and every step — from the qualified manufacturer abroad to your bench or production line — is auditable.

We don’t ask you to believe promises. We ask you to examine our documents, our process and our service. That is how trust is built in the pharmaceutical market: with proof, not talk.

Mission

To give Brazilian compounding pharmacies and pharmaceutical manufacturers direct access to the world’s best ingredients, with absolute traceability, ANVISA compliance and the agility the market demands.

Vision

To redefine the standard of pharmaceutical ingredient importing in Brazil and become, by 2030, the most trusted partner of compounding pharmacies and industry in Latin America.

Values

Non-negotiable quality — no batch comes in without complete documentation. Radical transparency — protocol, timeline and origin visible from start to finish. Speed with rigor — never fast at the expense of compliance. ANVISA as our foundation — the standard as our baseline, not an obstacle. True partnership — we grow when your business grows.

Portfolio

A complete line of ingredients

A broad portfolio of pharmaceutical ingredients for industry and compounding, with traceable origin and rigorous quality control.

APIs

High-purity active ingredients for a broad range of therapeutic classes.

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Raw materials

Pharmaceutical raw materials with traceable origin.

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Excipients and adjuvants

Vehicles and adjuvants for formulation.

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Peptides

High-purity peptides, supplied exclusively as ingredients to licensed establishments.

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Compounding supplies

Ingredients intended for compounding pharmacies.

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Controlled substances

Substances subject to special control (Ordinance 344/98).

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Medical devices

Medical devices with ANVISA clearance

Beyond pharmaceutical ingredients, Levisa imports and distributes healthcare materials and products registered or notified with ANVISA — with the same traceability and quality rigor as our API operation.

Consumables and disposables

Syringes, needles, gloves, dressings and infusion devices for the daily routine of pharmacies, clinics and healthcare services.

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Healthcare materials

A broad portfolio of healthcare materials and products, serving licensed establishments across Brazil.

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ANVISA compliance

Products registered or notified with ANVISA, covering the applicable risk classes, with complete technical documentation.

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Quality assurance and certifications

Operation fully licensed by ANVISA

The operation holds the licenses and authorizations required to work with pharmaceutical ingredients in Brazil — import, storage and distribution licensed by ANVISA (AFE No. 1.436.669 and Special Authorization No. 1.437.084), including substances under special control (Portaria SVS/MS nº 344/98). Distribution follows the Good Practices of RDC 204/2006.

Every API we distribute ships with complete technical documentation: CoA, SDS and analytical reports.

Qualified suppliers

Ingredients imported from audited manufacturers abroad.

Regulatory compliance

Operation fully licensed by ANVISA.

Quality control

Testing to the Brazilian Pharmacopoeia in force and recognized official compendia.

This website is intended exclusively for compounding pharmacies, distributors and ANVISA-licensed professionals. We do not sell directly to the public.

Cold chain and traceability

Controlled temperature from origin to your bench

Qualified storage, validated transport and online temperature and humidity monitoring at every step. From shipment to delivery, every batch travels with sensors recording conditions in real time — and you track it all.

Climate-controlled pharmaceutical ingredient storage area with sealed drums, reagent bottles and monitored pharmaceutical refrigerators
Climate-controlled area with continuous temperature and humidity control
Qualified thermal container with vials and a temperature and humidity monitoring sensor
Shipment in qualified thermal packaging, with a monitoring sensor

Monitored storage

Climate-controlled area with strict temperature (15–25 °C) and humidity control. Thermolabile products in dedicated 2–8 °C pharmaceutical refrigerators, with continuous logging and alarms.

Validated transport

Qualified thermal packaging and audited carriers for each temperature range.

Online monitoring

Sensors on every shipment stream temperature and humidity in real time, with a complete history per batch.

You are in control

As soon as the product leaves our storage area, you follow tracking and monitoring data through to receipt, with a data-logger report per batch.

Regulatory radar

ANVISA and the compounding sector

Tracking the main regulatory updates on compounding pharmacies and pharmaceutical ingredients.

13 MAY 2026

ANVISA approves the 8th edition of the Brazilian Pharmacopoeia

The new edition brings 19 new monographs and methods, 122 revisions and 203 technical corrections — the quality reference for ingredients and compounded medicines.

14 APR 2026

ANVISA drafts new rules for compounding GLP-1 pens

The draft technical note covers traceability, qualification of manufacturers and suppliers, and minimum quality-control testing along the chain.

06 APR 2026

New measures against irregularities in importing and compounding weight-loss pens

The agency flags the risks of ingredients without identified origin and composition, and announces rule reviews and stepped-up enforcement.

06 MAR 2026

ANVISA takes enforcement action against four compounding pharmacies

Actions include sales suspension and product seizure for non-compliance with Good Compounding Practices.

03 FEB 2026

ANVISA publishes rules for medical cannabis production

Four resolutions regulate production in Brazil; a specific rule for compounding pharmacies will follow.

Institutional curation by the Levisa Pharma regulatory radar. Last updated: August 2026.

Frequently asked questions

FAQ

Who can buy from Levisa Pharma?

We serve compounding pharmacies, distributors and ANVISA-licensed professionals exclusively. We do not sell directly to the public.

Is Levisa’s operation licensed by ANVISA?

Yes. The operation holds the required licenses and authorizations — AFE No. 1.436.669 and Special Authorization No. 1.437.084 — to import, store and distribute pharmaceutical ingredients in Brazil, including substances under special control (Ordinance SVS/MS 344/98).

What technical documentation comes with the ingredients?

Every API we distribute ships with complete technical documentation: Certificate of Analysis (CoA), SDS and analytical reports.

How is quality control performed?

Ingredients are imported from audited manufacturers abroad, qualified under API Good Manufacturing Practices (RDC 654/2022). Quality-control testing follows the Brazilian Pharmacopoeia in force and recognized official compendia, and distribution complies with the Good Practices of RDC 204/2006.

How do storage and the cold chain work?

Storage is qualified, with a cold chain and multi-temperature areas monitored 24/7, ensuring compliance and traceability at every step.

What is the delivery coverage?

We distribute nationwide, delivering to customers across Brazil.

How do I request a quote?

Via our sales WhatsApp (+55 11 99610-6253), the quote form on this page, or by e-mail at vendas@levisapharma.com.br. Our team will get back to you.

Contact and quotes

Let’s talk

Our team is ready to serve manufacturers, distributors and compounding pharmacies. Fill out the form and we will send your request straight to our sales team on WhatsApp.

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or e-mail us: vendas@levisapharma.com.br