Regulatory framework
Framing of company, activities and need for AFE/AE when applicable.
Support for companies that manufacture, import, distribute or market sanitizers and for establishments that need to organize their hygiene system and products.
Request technical evaluationFrom risk classification to batch: regulation for sanitizers with real technical control. Sanitizers require clearly separating regularization of the company and regularization of the product. The activity may require federal sanitary authorizations and local licenses; the product needs to be framed by the purpose, risk, composition and claims. The consultancy structures this architecture before developing labels or launching the portfolio.
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.
Framing of company, activities and need for AFE/AE when applicable.
Product classification and regularization route.
Formula, specifications, raw materials and packaging compatibility.
Good manufacturing practices, process control and batch release.
Labeling, efficacy claims and supporting documentation.
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 sanitizers and hygiene.
Good practices, SOPs, records, traceability, cleaning, supplier control, waste, storage and response to deviations need to be executable and demonstrable.
We gather answers to questions that usually appear before hiring a consultancy, initiating adjustments, filing documents or receiving an inspection.
No. They are different instruments, issued by different authorities according to the activity.
The form of regularization depends on the category and risk of the product.
Efficacy claims need to be compatible with regularization and supported by the required documentation/tests.
The starting point is a diagnosis of the current stage of sanitizers and hygiene: 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 sanitizers and hygiene 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.
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.
Product and risk matrix.
AFE/licensing checklist.
Batch specifications and controls.
GMP/SOPs Manual.
Technical review of claims and labeling.
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.
Portfolio regulatory screening.
Documentary diagnosis of the company.
GMP structuring and quality control.
Product dossier and label review.
A visual object created to represent the points that need to be discussed in a sanitizing and hygiene consultancy: risk, process, evidence and decision.
Claim disinfectant without proper support.
Product classification and regularization route.
Product and risk matrix.
Product dossier and label review.
The objective is to anticipate technical, documentary and regulatory incompatibilities before they become a requirement, redone work, stopped batch or protocol delay.
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.
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.
Claim disinfectant without proper support.
Changed formula without post-regularization evaluation.
Mixture of incompatible or unspecified raw materials.
Label with instructions for use that create risk or go beyond the approved purpose.
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.”
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