Classification and standard
Inventory of procedures and risk classification.
Support for service classification, licensing, infrastructure, equipment, products, waste and sanitary routines of aesthetics and beautification.
Request technical evaluationProfessional aesthetics requires sanitary control proportional to the procedure performed. The risk of an aesthetic service depends on concrete procedures, invasiveness, equipment, products and waste generation. Anvisa Technical Note No. 2/2024 reinforces the need to observe the applicable health standards. The consultancy starts with the inventory of procedures and creates a matrix of requirements per room, equipment, input and routine.
The scope is defined from the business stage. Hiring can begin with diagnosis and framing and evolve to documentation, adequacy, implementation, training, protocol and technical monitoring.
Inventory of procedures and risk classification.
Sanitary licensing and local physical requirements.
Processing/sterilization of materials when applicable.
Regularity and indication of use of equipment, cosmetics and health products.
PGRSS and safety in the management of sharps/waste when generated.
A visual object created to represent the points they need to talk about in an aesthetics and beauty consultancy: risk, process, evidence and decision.
Use of product or equipment outside the authorized purpose.
Sanitary licensing and local physical requirements.
Matriz procedimento × requisito.
Pre-inspection and adequacy plan.
Sanitary licensing is carried out within the scope of the National Health Surveillance System and may be conducted by the municipal or state authority, according to local organization, activity and risk. Regularization of the establishment and regularization of the product are different fronts.
Sanitary licensing, structure, flows, technical responsible when applicable, procedures and operational conditions are evaluated according to the activity and the local authority.
When there is a product subject to regularization, the consultancy separates product requirements, labeling, composition, dossier and communication/registration applicable to aesthetics and beauty.
Good practices, SOPs, records, traceability, cleaning, supplier control, waste, storage and response to deviations need to be executable and demonstrable.
The analysis confronts applicable requirement, project, documents, actual routine, records and business objective. The focus is on identifying cause and priority, not just listing to-dos.
Use of product or equipment outside the authorized purpose.
Single-use item reprocessing.
Shared room with incompatible procedures.
Lack of traceability of batches of products used in procedures.
The final list depends on the contracted scope and the stage of the business. The goal is for each delivery to have a practical function: guide the team, support the protocol, respond to the requirement, register control or demonstrate compliance.
Matriz procedimento × requisito.
Checklist of equipment and products.
Cleaning/processing SOPs.
PGRSS when applicable.
Documentation script for license.
The schedule is adjusted to the dependencies of the client, the project and the competent body. Each phase needs to produce a decision, document, adequacy or verifiable evidence.
Map of procedures and risks.
Room/equipment audit.
Structuring of SOPs and records.
Pre-inspection and adequacy plan.
We gather answers to questions that usually appear before hiring a consultancy, initiating adjustments, filing documents or receiving an inspection.
No. Procedures, equipment and invasiveness change requirements and must be evaluated individually.
No. The possibility depends on the manufacturer's indication and the rules applicable to the product.
Sanitary licensing is carried out within the scope of the SNVS, in general by the competent local health authority.
The starting point is a diagnosis of the current stage of aesthetics and beauty: activity, location, products/services, facilities, existing documents and business purpose. From this, PITRIO defines the regulatory route, the pending issues and the work sequence without promising a rite that depends on the competent authority.
The need depends on the framework. In the diagnosis, we evaluated records/licenses, design or layout, memorials, procedures, controls, labels, evidence and documents of the technician in charge. The final list is specific to aesthetics and beauty and to the competent body.
Sanitary licensing is carried out within the scope of the National Health Surveillance System and may be conducted by the municipal or state authority, according to local organization, activity and risk. Regularization of the establishment and regularization of the product are different fronts.
The strategy depends on the applicable process. In some cases the design and documents precede the final work; in others, the authority requires verifiable conditions in the establishment. The consultancy organizes this sequence to reduce rework.
Yes, when hired in scope. Follow-up may include protocol, organization of evidence, analysis of requirements, preparation of responses, review of documents, and technical support for adjustments. The final decision, official deadlines and inspection remain the responsibility of the public agency.
Sanitary licensing is carried out within the scope of the National Health Surveillance System and may be conducted by the municipal or state authority, according to local organization, activity and risk. Regularization of the establishment and regularization of the product are different fronts.
Official reference used to validate competence, concept or requirement. In the project, the current version and the complementary acts are checked according to the specific case.
Official reference used to validate competence, concept or requirement. In the project, the current version and the complementary acts are checked according to the specific case.
Official reference used to validate competence, concept or requirement. In the project, the current version and the complementary acts are checked according to the specific case.
Official reference used to validate competence, concept or requirement. In the project, the current version and the complementary acts are checked according to the specific case.
The objective is to anticipate technical, documentary and regulatory incompatibilities before they become a requirement, redone work, stopped batch or protocol delay.
Send city/State, activity, products or services, current situation, existing documents and business purpose. Based on this information, we can delimit the problem, identify the regulatory route and propose a consulting scope compatible with the stage of your business.
Companies throughout Brazil rely on PITRIO to achieve sanitary compliance and excellence in food safety.
“PITRIO simplified the entire registration process and helped us obtain the Inspection Seal. Today we sell safely to the whole country through SISBI.”
“The trainings of GMP and HACCP have raised the quality and reduced our contamination risks. Professionalism and exemplary technical mastery.”
“Agile technical team. Labeling advice has put us ahead of the competition, ensuring compliance with the new ANVISA RDCs.”
Join over 200 regulated industries. REQUEST TECHNICAL REFERENCES