MYCrave Consultancy & Services

Institutional IP · Evidence, not outcomes

We will not promise you a grade — and you should distrust anyone who does

Accreditation readiness through IPR

Assessment frameworks look at innovation, research output and intellectual property. A functioning IP cell produces exactly the documented evidence those frameworks ask for — filings, policy, process and training records, with dates attached. What it cannot do is decide your result.

70+IP cells established
22,000+IPR filings
4,200+Seminars & workshops
21+States covered

Start here

The honest position, stated first

This page exists because the category attracts overclaiming, and we would rather lose the enquiry than make a promise nobody can keep.

What is true

  • Assessment frameworks do look at innovation, research and IP output
  • Filed and granted rights are objective, dated, verifiable evidence
  • A written IP policy and disclosure process are documentation panels ask for
  • Training delivered and technology transferred both leave a paper trail
  • An institution with these can evidence its innovation activity properly

What is not

  • That IP activity determines an accreditation grade
  • That a number of filings maps to a score
  • That any firm can influence an assessment outcome
  • That last-minute filings before a visit will read as genuine activity
  • That this is a substitute for the things frameworks weigh far more heavily

The line we hold, on this page and everywhere else: strong IP management can support institutional evidence for accreditation and ranking submissions, but it does not guarantee any accreditation result.

The material

What a working IP cell actually evidences

Six categories of documentation, all of them generated as a by-product of the cell doing its normal job.

Filings

IP attributable to the institution

Patents, designs and copyrights with application numbers, dates, status and named inventors.

Policy

An approved IP policy

Ownership, revenue sharing and collaboration terms, formally adopted rather than drafted and shelved.

Process

A documented disclosure route

The form, the assessment step and the decision record — showing the process is real and used.

Training

Capability building, recorded

Sessions delivered, attendance, coverage across departments, and faculty development completed.

Transfer

Industry engagement

Licensing and technology transfer activity, with agreements and outcomes rather than intentions.

Continuity

Year-on-year activity

The thing panels actually notice: a consistent record over time, not a spike before a visit.

Boundaries

What this cannot do, in plain terms

If a provider tells you filings will lift your grade, ask them to put it in writing. They will not, because nobody can.

No influence

Nobody can influence a panel

Assessment bodies are independent. No consultancy has, or should have, any route into that decision.

No shortcut

Volume filed late reads as exactly that

A cluster of applications weeks before a visit is visible in the dates, and it does not read as an innovation culture.

Not the main weight

IP is one input among many

Teaching, learning outcomes, governance, infrastructure and student progression carry far more weight than IP output does.

No guarantee

Evidence is not an outcome

Good documentation lets you evidence what you did. It cannot promise what a panel concludes.

The work

How we build the evidence base

Note the order. The filings come out of the cell working, not the other way round — which is also why the record reads as genuine.

01

Institutional consultation

What exists today, what the submission cycle looks like, and how much runway there is before it.

02

Gap assessment

What the frameworks ask for against what you can currently evidence. This is usually shorter and more specific than people expect.

03

Policy and process

An IP policy drafted or reviewed and formally adopted, with a disclosure route people can actually use.

04

Capability building

Awareness sessions and faculty development, delivered across departments and recorded properly.

05

Invention identification

A sweep of existing project and research output for what is still protectable — where the first genuine filings come from.

06

Filing and prosecution

Drafted, filed and carried through examination, so the record shows outcomes rather than only applications.

07

Documentation pack

Everything compiled in a form the submission can draw on directly, with dates, numbers and evidence attached.

Expectations

Timeline, honestly

The single most useful thing on this page: start earlier than you think you need to.

Fast, and in our control

MYCrave’s part

  1. Gap assessment1–2 weeks
  2. Policy drafted and ready for adoption2–4 weeks
  3. Training deliveredper the agreed calendar
  4. Drafting and filing per invention1–3 weeks each
Statutory, not in anyone’s control

The government’s part

  1. Publication of applications~18 months from priority
  2. Examination after RFEstatutory queue
  3. Grantnot fixed
  4. Design and copyright registrationOffice timelines
Scoped per institution — no standard price list

What an accreditation-readiness programme costs

Scoped against your submission cycle and what already exists. If you have twelve months, the work looks very different from three — and if you have three, we will tell you honestly what can and cannot be evidenced in that time.

Official Government fees for filings are quoted separately from professional fees, and academic institutions attract reduced official fees in several categories. To repeat the position: this work supports institutional evidence for accreditation and ranking submissions. It does not guarantee any accreditation result.

How long until your submission

Runway is the biggest single factor, and it is the one nobody can extend.

What already exists

An adopted policy and past filings shorten the work considerably.

Size and number of departments

How wide the training and invention drive have to run.

How many filings are realistic

Set against genuine output, not a target number picked to fill a table.

Whether we compile the pack

Evidence generated, or evidence generated and assembled into submission-ready form.

Straight answers

Frequently asked questions

Will IP filings improve our NAAC or NIRF result?

Nobody can tell you that, and you should treat anyone who does with suspicion. What is true is narrower and still useful: these frameworks look at innovation, research and IP among many other things, and a functioning cell produces objective, dated evidence in that category where an institution might otherwise have none. Strong IP management can support institutional evidence for accreditation and ranking submissions, but it does not guarantee any accreditation result.

How many filings do we need?

There is no number, and any provider quoting one is inventing it. What reads well is consistency and genuineness — activity spread across departments and across years, with outcomes attached, rather than a batch filed shortly before a visit. An institution with a modest number of well-documented filings arising from real research usually evidences better than one with a sudden cluster.

We have a submission in three months. Can you help?

Yes, but with a realistic scope. In three months you can adopt a policy, deliver training with proper records, run an invention identification drive across existing output, and file on what that surfaces. What you cannot do is produce grants, because examination timelines are statutory and outside anyone’s control. We will tell you at the start what is achievable in your window rather than after you have paid for it.

Is filing a batch of applications before a visit a good idea?

No, and it is worth saying plainly. Applications carry dates, and a cluster immediately before an assessment is visible for what it is. It also costs real money in official fees for filings that may have had little assessment behind them. The better use of the same budget is a policy, a disclosure process and a training record — all of which evidence an innovation culture rather than a reaction to a deadline.

Do you write the submission for us?

No. We produce and compile the IP evidence — filings with numbers and dates, the adopted policy, the disclosure process, training and attendance records, and transfer activity — in a form your submission can draw on directly. The submission itself is written by the institution, by people who know the whole picture. IP is one section of many.

What if our departments have no research output to protect?

That is worth establishing early, and the invention identification drive is how. In practice most institutions have considerably more protectable work than they think, sitting in completed projects, prototypes and theses that were assessed academically and never assessed for protectability. If a genuine sweep finds nothing, we will tell you that rather than filing on weak material to produce a number.

Does this replace the IP Cell service?

No — it is the same underlying work aimed at a specific deadline. The evidence is a by-product of a cell doing its normal job: assessing disclosures, training people and filing on what is worth filing. If you are not under submission pressure, the IP Cell service is the right starting point and produces the same documentation without the compression.

Talk to an IP expert

Start earlier than you think you need to.

Tell us your submission cycle and what exists today, and you will get an honest read on what can be evidenced in the time available — including if the answer is “less than you hoped”.

Call WhatsApp Free consultation