First, what takes longest
Quality culture, risks and opportunities and change management need months of real behavior to be demonstrated. That is why they start first. Wording adjustments are resolved at the end, in a single review.
Two consulting services: transition from the 2015 edition in 26 weeks or direct certification in 52 weeks. A phased plan, a guide every week and the signature of Ing. Freddy Brun on every closed week.
What we do not do. We do not promise certification: the certification body decides. We offer method and weekly control, with the signature of Ing. Freddy Brun on every closed week; your organization builds the evidence.
WHY NOW
The ISO 9001:2015 transition deadlines are published. What cannot be compressed is the time a system needs to generate real evidence that it works.
The 2026 edition of ISO 9001 is published. From here, organizations can start to transition.
Until this date, certification bodies can certify or recertify against the 2015 edition.
A 2015 certificate that has not transitioned stops being valid.
Source: Global ACI, Transition requirements for ISO 9001:2026 (TECH-3-TR). Some bodies set slightly different dates: each body confirms the effective date.
Your 2015 certificate is valid until its expiry, and never beyond 30 Sep 2029. After 31 Mar 2028, the last day to certify to the 2015 edition, 2015 certificates are no longer issued or recertified: if your recertification falls after that date, it has to be against the 2026 edition. The transition audit needs a 26-week plan with real evidence, which is why we plan backwards from the date your certification body sets.
SERVICE A AND SERVICE B
The difference is not the quality of the support but where you start from.
For organizations with a valid ISO 9001:2015 certificate that want to reach the transition audit with an updated system and evidence.
Does not include the certification decision: that belongs to the certification body.
See the transition planFor organizations certifying for the first time: design, implementation and an operating period with records before the stage 1 and stage 2 audits.
Does not include the certification decision: that belongs to the certification body.
See the certification planSwipe to see the whole table
| A · ISO 9001:2015 2026 transition | B · ISO 9001:2026 certification | |
|---|---|---|
| Who it is for | Organizations certified to ISO 9001:2015 | Organizations certifying for the first time |
| Duration | 26 weeks | 52 weeks |
| Work + reserve weeks | 24 + 2 | 48 + 4 |
| Phases | 6 | 7 |
| Management decision gates | 6 | 7 |
| Visible milestones | 7 | 12 |
| Weekly guides | 24 | 48 |
| Ends with | Transition audit by the certification body | Stage 1 and stage 2 audits by the certification body |
| Starting point | A valid ISO 9001:2015 certificate and a working system | First certification, with real activity that generates records |
Already know which one fits? The initial assessment confirms it in one conversation.
Initial assessment with Ing. Freddy BrunHOW WE WORK
The 5 Key Steps Method for Value Creation, applied to ISO 9001:2026.
Quality culture, risks and opportunities and change management need months of real behavior to be demonstrated. That is why they start first. Wording adjustments are resolved at the end, in a single review.
We work on each process with all the requirements that touch it. The organization does not go back over the same thing four times.
Top management follows results by phase, not chapter progress. Each phase closes with a phase gate: top management decides, with defined criteria, whether to continue or adjust.
The phase order is a professional criterion of Buenas Prácticas, not a requirement of the standard. The standard only clarifies two things: that documentation does not need to be aligned to the structure of its clauses (clause 0.1) and that this structure is not meant as a model for documenting the organization's policies, objectives or processes (Annex A, A.2). Within that freedom, we order the work by the time each requirement needs to generate evidence.
Buenas Prácticas
At the start of each week, Buenas Prácticas delivers a working guide with four questions: what we do this week and why, what the standard asks, how we build it and how we know it is right. Each question is answered on two levels: "In plain words", for anyone in the organization, and "For specialists", with the technical precision Quality needs. Each statement carries a label: REQUIREMENT (the standard demands it), GUIDANCE (it comes from a note or Annex A) or BP PRACTICE (a recommendation from Buenas Prácticas).
Organization
The organization builds its own system. Its teams own the processes and know them best: for the key documents they start from a base model provided by Buenas Prácticas and adapt it to their reality. The system reflects how they work, not a generic model.
Buenas Prácticas
At the end of the week, Buenas Prácticas reviews what was produced against the guide's checklist and against what an auditor usually looks at. When the deliverable starts from a Buenas Prácticas base model, the week closes with top management approval plus the checklist, applied to the version the organization adapted: Buenas Prácticas does not control its own model. If everything is in order, the week closes with the signature of Ing. Freddy Brun; if not, observations are returned within the committed time, before moving on.
Every week is a joint responsibility of the Organization and Buenas Prácticas.
Every week, a guide with the same four questions. Each one is answered twice: in plain words and for specialists. The plain column simplifies, never distorts.
Anyone in the organization
What needs to be done, why it matters and how you can tell it works, with no jargon and with a before / now example.
Quality, internal auditors and top management
What the standard asks, with clause and subclause, what changed compared with 2015, which reference frameworks support it and the criteria Buenas Prácticas uses to control it.
The standard requires it (it uses "shall").
It comes from a note or Annex A of the standard, or from a guidance standard: it helps, but does not oblige.
A Buenas Prácticas recommendation based on its experience. It is not a requirement of the standard.
A week is closed when Buenas Prácticas' control approves the guide's checklist. If the deliverable starts from a Buenas Prácticas base model, the organization's top management also approves the adapted version; the control is applied to that version, not to the model. If it is not approved, Buenas Prácticas returns observations within the committed time and the week stays open until they are resolved.
Buenas Prácticas returns the observations in writing, within the committed time, indicating what is missing and why. The organization resolves them and the control is repeated.
On the progress dashboard, top management sees which weeks are closed, which are in progress and which fell behind, without having to review the deliverables one by one.
Every closed week carries the approval signature of Ing. Freddy Brun.
At the end of each phase there is a gate: a short meeting in which top management decides, with criteria defined in advance, whether to continue with the plan or adjust it.
The criteria for each gate are in the plan. The decision always belongs to the organization's top management; Buenas Prácticas provides the analysis and the recommendation.
Passing a phase gate is not the same as obtaining certification: the decision to certify is made exclusively by the certification body.
No 26- or 52-week schedule holds up without margin: there are holidays, vacation shutdowns, production peaks, people who fall ill and bodies that reschedule. That is why the plan includes reserve weeks: 2 in Service A (24 of work and 2 of reserve) and 4 in Service B (48 of work and 4 of reserve).
Survey and gap analysis against the 2026 edition.
Prioritization of gaps according to the time each requirement needs to generate evidence.
Plan by phases and weeks, with a phase gate at the close of each phase.
Weekly cycle: guide, build and control.
Internal audit, management review, mock audit and support during the certification body's audit.
SCHEDULE
Each phase closes with a gate where management decides (the diamond). “R” marks reserve weeks and “A” the external audit, whose date is set by the certification body.
Swipe to see all weeks
Swipe to see the whole table
| Phase | Weeks | Milestones | Gate |
|---|---|---|---|
| F1 · Kick-off and assessment | W01–W03 | W01 Project start W03 Assessment delivered | W03 · Do we continue with the transition plan? |
| F2 · Culture, leadership and risks | W04–W10 | W10 Culture and risks implemented | W10 · Are culture and risks under way so that evidence starts to be generated? |
| F3 · Context, changes and knowledge | W11–W14 | — | W14 · Do we move on to adjusting operations and measurement? |
| F4 · Customers, suppliers and measurement | W15–W18 | W17 System updated | W18 · Are we ready to audit the system internally? |
| F5 · Internal verification | W19–W22 | W21 Internal audit completed W22 Management review | W22 · Do we close the verification and move on to final preparation? |
| F6 · Documentation close-out and transition audit | W23–W26 | W26 Transition audit | W25 · Do we go to the transition audit with the system ready? |
Swipe to see all weeks
Swipe to see the whole table
| Phase | Weeks | Milestones | Gate |
|---|---|---|---|
| F1 · Kick-off and assessment | W01–W03 | W01 Project start W03 Assessment delivered | W03 · Do we continue with the proposed scope and schedule? |
| F2 · Context, leadership and planning | W04–W11 | W11 Strategic foundations approved | W11 · Do we approve the strategic foundations of the system? |
| F3 · System design and documentation | W12–W27 | W26 System documented | W27 · Do we approve the documented system and move on to implementing it? |
| F4 · Implementation and training | W28–W33 | W28 System launch W33 System in operation | W33 · Does the system work as documented? |
| F5 · Operation with records | W34–W39 | W38 Operating period completed | W39 · Are we ready to audit the system internally? |
| F6 · Internal verification | W40–W44 | W41 Internal audit completed W43 Management review | W44 · Do we go to stage 1 of the certification audit? |
| F7 · Certification | W45–W52 | W46 Stage 1 audit W50 Stage 2 audit W52 Project close | W49 · Do we go to stage 2 of the certification audit? |
Passing a phase gate is not the same as obtaining certification: the certification decision is made exclusively by the certification body.
WHAT YOU GET, WHAT IS ON YOUR SIDE, TIME COMMITMENT
Phase columns: weekly average per phase. “Peak”: the role’s heaviest week. “Total”: project hours per person, excluding reserve weeks. These are estimates and are adjusted after the initial assessment. Weekly working session with your counterpart: a Meet session of 60 to 90 minutes per week, with WhatsApp support from 8 am to 8 pm.
| Role | F1 | F2 | F3 | F4 | F5 | F6 | Avg. | Peak | Project total |
|---|---|---|---|---|---|---|---|---|---|
| Top management | 1.5–2.5 | 1.5–2.5 | 1.5–2.5 | 1.5–2.5 | 1.5–2.5 | 2.5–3.5 | 1.5–2.5 | 6 | 38–63 |
| Quality Manager | 3.5–5 | 4–6 | 4.5–6.5 | 4–6 | 4–6 | 6–8.5 | 4–6 | 12 | 100–149 |
| Process owners | 1.5–2 | 2–3.5 | 2.5–3.5 | 3–4.5 | 2–3 | 3–5 | 2–3.5 | 6 | 53–83 |
| Staff | 0.5–1 | 0–0.5 | 0.5 | — | — | 1.5–2.5 | 0.5 | 4 | 8–14 |
| Internal auditors | 1–1.5 | — | — | — | 5–7.5 | 1.5–2 | 1–1.5 | 12 | 26–39 |
Totals do not include the 2 reserve weeks.
| Role | F1 | F2 | F3 | F4 | F5 | F6 | F7 | Avg. | Peak | Project total |
|---|---|---|---|---|---|---|---|---|---|---|
| Top management | 1.5–2.5 | 2–3 | 1–2 | 1.5–2.5 | 1–2 | 1.5–2.5 | 2–3 | 1.5–2.5 | 6 | 71–120 |
| Quality Manager | 3–5 | 4–6 | 4–6 | 4–6 | 4–6 | 4–6 | 6–8.5 | 4–6.5 | 12 | 200–300 |
| Process owners | 1.5–2.5 | 2–3 | 2.5–4 | 2.5–3.5 | 2–3.5 | 2.5–4.5 | 2.5–4.5 | 2.5–3.5 | 6 | 111–177 |
| Staff | — | — | <0.5 | 1–2 | — | — | 1–1.5 | 0.5 | 5 | 14–24 |
| Internal auditors | — | — | — | 1.5–2 | 0.5–1 | 4–6 | 0.5–1 | 0.5–1 | 12 | 31–47 |
Totals do not include the 4 reserve weeks.
With your certification body’s date, the plan is calculated backwards.
Initial assessment with Ing. Freddy BrunSCOPE AND CONDITIONS
We put it in writing before starting so that “done” means the same thing for everyone.
SAMPLE GUIDE
Every week, a guide with the same four questions. Each one is answered twice: in plain words and for specialists. This is the week 5 guide of Service A; the “before / now” examples are illustrative and do not correspond to real companies.
Week 5 · Service A
The sample guide is a client deliverable and is shown in its original language, Spanish.
Esta semana la Dirección define qué significa «hacer bien las cosas» en tu organización, cómo se nota a diario, y lo deja en una declaración corta con conductas e indicadores.
Importa porque podés tener todo escrito y fallar igual: si avisar un error trae problemas, los errores se esconden. La norma 2026 pide a la alta dirección promover dos cosas: cultura de la calidad y comportamiento ético.
En una metalúrgica de 60 personas
A.5.1 da a la alta dirección un rol fundamental en promover la cultura de la calidad; la ética en decisiones, acciones e interacciones puede incidir en cualquier aspecto de la calidad.
Riesgo: sin conductas observables hay poca evidencia objetiva del inciso; el sistema luce bien en papel y falla en la práctica.
Vínculo: BP propone llevar los indicadores de conducta a la revisión por la dirección como evidencia de rendición de cuentas sobre la eficacia.
La cláusula 5.1.1 enumera cómo la alta dirección demuestra liderazgo. Esta semana importan dos:
Una nota de la norma aclara que cultura y ética se ven en valores compartidos, actitudes, prácticas y acciones. BP agrega: que se observen a diario.
Como parte de su liderazgo y compromiso, la alta dirección debe promover el comportamiento ético y la cultura de la calidad.
Debe promover tanto el pensamiento basado en riesgos como el basado en oportunidades.
Según la Nota 2, los dos conceptos del inciso i) se hacen visibles en valores compartidos, actitudes, prácticas y acciones.
Respecto de 2015: inciso nuevo. En 2015 la cultura solo aparecía en el contexto interno (4.1 Nota 3), no como compromiso de liderazgo.
Respecto de 2015: el pensamiento basado en riesgos ya figuraba en 5.1.1 d). Lo nuevo son las oportunidades, que 6.1.2 y 6.1.3 tratan por separado.
Respecto de 2015: el Prólogo cuenta la cultura y la ética entre los cambios principales, sobre todo en liderazgo (5.1.1), toma de conciencia (7.3) y ambiente (7.1.4).
El inciso no exige información documentada ni formato. BP propone la declaración porque deja evidencia fechada y aprobada.
Valores: de 3 a 5, cada uno con una conducta que un tercero pueda observar. Los genéricos («excelencia») no sirven.
Oportunidades: la declaración puede registrar cómo las promueve la Dirección; sus acciones (6.1.3) se trabajan en las semanas 8 a 10.
PL-05-declaracion-cultura.docx
WHAT PEOPLE USUALLY ASK
No. The decision to certify or to keep a certificate belongs exclusively to the certification body. Our job is to help you get prepared: with method and weekly control, and with the signature of Ing. Freddy Brun on every closed week; your organization builds the evidence.
Every plan includes an estimated time commitment table by role (top management, Quality Manager, process owners, staff and internal auditors), in ranges of hours per week per person, with the heaviest week marked; you can see it above. It is adjusted in the assessment with your team’s real availability, and the plan includes reserve weeks to absorb delays.
Every week you receive a working guide with four questions (what we do and why, what the standard requires, how we build it and how we know it is right), a working session with your team, a review of what was produced with written feedback within the committed time, and the signature of Ing. Freddy Brun when the week is closed. We also facilitate the key workshops and milestones: quality culture, internal audit, mock audit and preparation for the certification body’s audit. Your team builds the system because it owns the processes: if a third party writes it, it does not reflect how you work and is hard to sustain in an audit.
We do not comment on other proposals. Our criterion is to order the work by what takes longest to generate evidence: quality culture, risks and opportunities and change management need months of real behavior to be demonstrated, and the internal audit and management review must rest on that evidence. It is our professional criterion, not a requirement of the standard. If your certification body audits earlier, we do not promise the impossible: we calculate backwards from that date, see which weeks are compressed and which evidence ends up more recent, and top management decides whether to accept that risk.
The plan includes reserve weeks within the total: 2 in Service A and 4 in Service B, placed before the most sensitive milestones. There are written rescheduling rules: if a week slips, the nearest reserve is used; if the body changes the date, the plan is recalculated backwards; shutdowns, like the January one, are reported at the start and charged to the reserve. Every client receives a calendar with real dates, not generic weeks.
The plan is a framework that is adapted to your organization in two places: each weekly guide has a “Your organization” section with questions and data to fit it to your reality, and the diagnosis in the first weeks is when the plan is fitted to your case. The calendar also comes with your real dates. Above you can see a complete sample guide, and Ing. Freddy Brun’s background is on his page.
No. The 10-clause structure and the process approach are kept; specific requirements change. The organization updates what changed, and the gap analysis at the start sets out what.
According to the Global ACI TECH-3-TR document, until 30 Sep 2029. Some bodies set slightly different dates: your certification body confirms it.
According to Global ACI TECH-3-TR, until 31 Mar 2028, and those certificates stop being valid on 30 Sep 2029. The certification body confirms it.
No. The standard makes clear that this is not needed (clause 0.1 and Annex A, A.2). That is why we work each process with all the requirements that touch it.
It is Buenas Prácticas material. It explains the standard but does not replace it: the standard is obtained in its official edition (IRAM).
WHY BUENAS PRÁCTICAS
Buenas Prácticas is a team led by Ing. Freddy Brun, with over 30 years in industry. The method, the guides and the templates are our own and are applied the same way in every week of every service.

Buenas Prácticas adds professionals to the Associate Consultants Program: you work with your own clients using the BP method and guides.
PDF DOWNLOADS
Five documents to read, print or share with your management and your certification body. The PDFs are in Spanish.
Brochure for the 26-week service: phases, milestones and dedication.
Download PDFPDF · 2,4 MB · in Spanish
Brochure for the 52-week service: design, implementation and audits.
Download PDFPDF · 2,4 MB · in Spanish
One-page summary of the first step with Ing. Freddy Brun.
Download PDFPDF · 0,5 MB · in Spanish
Training material: what changed in ISO 9001:2026.
Download PDFPDF · 2,3 MB · in Spanish
Brochure for the program for consultants and auditors.
Download PDFPDF · 2,7 MB · in Spanish
Two steps. First, a 1-hour introductory talk with Ing. Freddy Brun, remote and free of charge, where he presents how we work in the service that fits you. Then the assessment: you complete a checklist, send us the documented information we ask for, and receive an initial assessment report with Strengths and Opportunities for improvement, useful even if you do not hire us.
You can also write to us at asistentebp73@gmail.com or on WhatsApp at +54 9 341 555-7944.
The contact form already has “ISO 9001:2026 · Initial assessment” selected. Once the date of the talk is confirmed we send you the assessment checklist, with the list of documented information to send; anything you do not know, mark as “Don’t know”.