Data is Life: Why DGPSI Treats Every Hospital as a Significant Data Fiduciary

The basic objective of the Digital Personal Data Protection Act (DPDPA) is to give individuals a right to protect their privacy through the regulated management of personal data while it is processed by third parties. How we arrived at that objective is itself a story of how our understanding of data has evolved — and that evolution is the key to seeing why hospitals are different.

In the first generation, personal data was understood technically: a set of binary data which the perceiver is able to read as information belonging to an identifiable individual. The concern of that era was the preservation of Confidentiality, Integrity and Availability — the familiar CIA triad of information security. Data was qualified as “sensitive” only when its loss could harm the individual, and protection meant securing the bits.

The second generation reframed data as money. As organizations searched for monetization strategies, digital marketing companies built their business on profiling data principals and linking that profile to advertising. Data became an asset to be valued and traded. It was at this stage that privacy protection surfaced as a public concern, and laws such as the DPDPA emerged to address it.

Because “privacy” is notoriously difficult to define, the DPDPA wisely declined to define it. Instead it prescribed certain measurable obligations on the processing of personal data and enforced them through a stringent penalty system. These are the obligations of the Data Fiduciary — the organization that, by determining the purpose and means of processing, is recognized as a trustee and is expected to take micro-level decisions in that fiduciary character. The Fiduciary’s journey therefore begins with a Notice that explains the purpose of collection and how the data will be used, followed by the capture of the data principal’s Consent.

The DGPSI frameworks recognized this changing perception and introduced Data Valuation as a key parameter in their compliance strategies. And it is precisely the question of valuation that brings us to the third generation — and to hospitals.

In a hospital, the personal data of a patient is not simply personal data that has a value to be monetized. It is representative of life itself. Any misuse or breach does not end in financial loss; it could endanger the life of the patient. Hence the axiom “Data is Money” is not valid for the healthcare sector. Here we need to treat Data as Life.

Note that valuation does not disappear in this third generation — it changes its denomination. The value of patient data is no longer measured in rupees of monetization but in the severity of harm to life. DGPSI’s Data Valuation parameter therefore remains central to healthcare compliance; only the currency changes.

This matters all the more because the DPDPA deliberately abandoned the category of “sensitive personal data” that earlier Indian rules had recognized. The statute applies a single, uniform standard to all personal data and refuses to place health data on a special pedestal. If the law will not elevate health data, then governance must. The responsibility of restoring the special status of patient data falls on the compliance framework, not on the statute.

This is the reasoning behind a deliberate DGPSI decision. The DPDPA grades the “significance” of a Data Fiduciary largely by scale — the volume and sensitivity of data and the breadth of risk to data principals — and leaves the designation of a Significant Data Fiduciary to government notification. But harm to life cannot be graded by scale. One life lost is not less significant than many lives lost. A small nursing home that endangers a single patient through a data breach has caused a harm no less grave than a large hospital chain. The volume-based test of significance, sensible for commercial data, is the wrong yardstick for life.

DGPSI therefore treats every hospital as a Significant Data Fiduciary — regardless of its size, the number of patients it serves, or whether the government has notified it as such. Under DGPSI, the threshold question “Am I a Significant Data Fiduciary?” has only one answer for a hospital: yes.

That elevation has a direct governance consequence. For an ordinary company, one can argue for a lean compliance team. The DPDPA makes a Data Protection Officer (DPO) a mandatory statutory function only for a Significant Data Fiduciary, while leaving the Chief Information Security Officer (CISO) as a best-practice function. On that footing, a general company could let the DPO be made responsible for DPDPA compliance and allow the CISO to continue focusing on what he is presently doing.

A hospital cannot be governed so simply. Once every hospital is treated as a Significant Data Fiduciary, the DPO becomes a full, mandatory function in each one. But the DPO cannot be placed on the pedestal of data protection responsibilities alone, because a hospital has a third officer whose role cannot be subordinated — the Patient Safety Officer (PSO).

The PSO’s functions are quasi-legal. They often protect the hospital and its doctors from liabilities arising out of unfortunate adverse events. This authority cannot be allowed to be pushed down by the DPO. One may debate whether the CISO can still be pushed down and the compliance left to the DPO and the PSO together. After giving weight to these sensitivities of governance, DGPSI has decided to retain a triumvirate — the DPO, the CISO and the PSO — as the compliance team in a hospital.

The wisdom of insisting on all three becomes obvious the moment a breach occurs. A single data breach in a hospital can trigger two clocks at once: the CISO must report the cyber incident to CERT-In within six hours, while the DPO must notify the Data Protection Board and the affected patients within seventy-two hours under the DPDP Rules. (The moment the data breach report is triggered the Patient  Safety event also gets triggered.) Two timelines, two regulators and two reporting formats have to be coordinated under pressure — which is exactly the coordination the triumvirate exists to provide. Leave one officer out, and the clock keeps running while the others stitch the response together.

The DGPSI-Hospital governance structure therefore retains an apex DPDPA governance body — which includes other stakeholders such as the CFO and the CMO, and is led by an Independent Director — with the triumvirate functioning as its sub-committee. Accountability to the regulator rests with the fiduciary through this apex body; the triumvirate is the coordinating engine beneath it, not a diffusion of responsibility. Externally, each of the three members maintains a distinct line of exposure: the DPO to the Data Protection Board (DPB), the CISO to CERT-In, and the PSO to the NABH accreditation authorities.

As regards the PSO’s remaining obligations, the call is for cooperation rather than competition. The PSO has to coordinate with the CISO and the CIO to establish a compliance architecture for NABH accreditation, without interfering with the DPO’s requirements under the DPDPA.

These distinctions grow sharper as hospitals adopt artificial intelligence. AI-assisted diagnosis, clinical decision support and the profiling of patient data fold the safety question and the data-protection question into a single question: an erroneous or biased model can endanger life exactly as a breach can. Governing such systems needs the safety lens of the PSO, the security lens of the CISO and the data-protection lens of the DPO acting together.

These changes need to be reflected in DGPSI-Hospital as an improvement to the framework — DGPSI-FULL with AI.

Naavi

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Attention Independent Directors

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Independent Directors and DPDPA Risk: Has the Institution Kept Pace with the Data Economy?

In corporate governance, Independent Directors play an important role in protecting shareholder interests. One of their core responsibilities is to oversee risks that may adversely affect the financial position and sustainability of the company.

Traditionally, this responsibility has been interpreted in the context of financial reporting, internal controls, statutory compliance, and operational risks. However, in today’s data-driven economy, such an interpretation is no longer sufficient.

Now, Data has emerged as one of the most valuable assets of modern enterprises. In many organizations, data is accumulated, processed, analyzed, and monetized long before its value is reflected in the financial statements. Consequently, Independent Directors can no longer limit their oversight to the integrity of financial reports. They must also understand the value, ownership, control, and governance of the organization’s data assets.

An unscrupulous management may undervalue, transfer, misuse, or otherwise compromise data assets in a manner that may not immediately appear as a financial irregularity. Yet the impact on shareholder value can be as significant as fraud, asset stripping, or money laundering. Unfortunately, many boards and Independent Directors are yet to recognize this dimension of governance.

The history of CIBIL provides an example worthy of study. The transfer of control over a valuable national data asset through changes in shareholding raised questions regarding the valuation and stewardship of data that had been contributed by Indian financial institutions. At the time, concerns were raised regarding the long-term implications for the banking sector and the country. However, the governance implications of transferring control over a strategic data asset did not receive the attention that a comparable transfer of tangible assets or financial resources might have attracted.

This raises a broader question: Are Independent Directors adequately equipped to oversee data governance risks?

The question assumes greater significance after the enactment of the Digital Personal Data Protection Act, 2023. Non-compliance with DPDPA can result in substantial financial penalties, reputational damage, regulatory action, and loss of stakeholder trust. DPDPA risk is therefore not merely a compliance issue; it is a board-level governance risk.

Schedule IV of the Companies Act, 2013 prescribes a Code for Independent Directors and specifies their roles, functions, and duties. These include safeguarding stakeholder interests, scrutinizing management performance, satisfying themselves regarding the integrity of financial information and risk management systems, and bringing an independent judgment to board deliberations.

Viewed in this context, oversight of DPDPA compliance naturally falls within the governance responsibilities of Independent Directors. They should be asking questions such as:

  • Has the organization identified and classified its personal data assets?
  • Has a DPDPA risk assessment been undertaken?
  • What is the potential financial exposure arising from non-compliance?
  • Are adequate governance mechanisms in place for consent management, data principal rights, breach response, and vendor oversight?
  • Is the Board receiving periodic reports on privacy and data protection risks?

These questions are now as important as questions relating to financial controls or statutory audits.

Having recently renewed my registration in the Independent Directors’ databank, I found myself reflecting on whether the objectives behind the institution of Independent Directors are being fully realized in the emerging data economy. It is also pertinent to ask whether sufficient emphasis is being placed on DPDPA governance in the training and continuing education programmes conducted for Independent Directors.

Over the last few years, we at FDPPI  have attempted to engage with board members and governance professionals through conferences, symposiums, and awareness programmes. We have consistently emphasized that DPDPA compliance should be viewed as a board responsibility and that Independent Directors should play a leadership role in assessing and monitoring DPDPA-related risks.

If the Independent Directors’ framework administered by the Indian Institute of Corporate Affairs is to remain relevant in the coming decade, it must incorporate data governance, privacy governance, AI governance, and DPDPA risk management as core elements of board oversight.

The institution of Independent Directorship was created to provide objective and independent supervision of management. In the digital economy, independence must extend beyond financial scrutiny to include stewardship of data assets and protection of stakeholder rights.

As someone associated with the Independent Directors’ databank, I consider it my duty to raise these concerns. I hope that the Indian Institute of Corporate Affairs will confirm that adequate steps have been taken to sensitise Independent Directors to DPDPA-related risks and to equip them with the knowledge necessary to discharge their responsibilities effectively in their respective organizations.

Naavi

 

 

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Consulting Doctors and their Status: DGPSI-Hospital

We have earlier discussed the need to recognize the Governance structure of DPDPA Compliance team including the PSO or the Patient Safety officer as one of the co-owners of the compliance requirements since every data breach is also a Patient Safety event. We therefore suggested that the team of CISO-DPO-PSO will be responsible for DPDPA compliance, NABH compliance and ITA 2000 compliance as an integrated compliance plan.

Another area of complexity that the hospitals find is in establishing the status of the consulting doctors, Subordinate hospitals and diagnostic  centres. Diagnostic centers operate independently and determine the clinical decisions and therefore the Patient Safety  actions.

Many hospitals provide support to subordinate hospitals in terms of telemedicine consultancy and some times remote surgery. In such cases the two entities need to settle their inter-se status as Joint Data Fiduciaries with  a recognized boundary for data responsibilities.

Hospitals also work with consulting doctors who are independent professionals and take independent decisions on how the patient data is processed and disclosed. Some doctors may have “Employment” status while most may not. In such cases the status of who is a data fiduciary and who is a joint data fiduciary is a matter to be taken into account.

Additionally most hospitals work under a brand sharing  program where there could be an umbrella brand that attracts the patients while the service is rendered independently by the franchisee hospitals. In such cases the  possibility of “Super Data Fiduciary” status for the  umbrella brand has to be also considered.

The DGPSI-Hospital framework therefore needs to cover these special situations.

Please send your views on these issues.

Watch out for more discussion.

Naavi

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Modified Intermediary Rules for publishers

Attention is drawn to the notice issued by MeitY on 21st  April 2026 related to the draft amendments to Information Technology (Intermediary Guidelines and Digital Media Ethics Code) Rules, 2021 in relation to strengthening intermediary compliance with clarifications, advisories and directions issued by the Ministry. (Refer here)

The last date for public comments  was 7th May 2026 which is well behind us.

So far no confirmation of the final rules has come from MeitY. 

The copy of the proposed draft rules are here. This should be read with the earlier consolidated rules published on 10th April 2026

An article which appeared in Indian Express today  flagging some of the key issues of  the rules is available here

While we await the release of the final rules, a brief review of the article of Indian express flag the following observations.

The proposed amendments represent a substantial expansion of governmental oversight over digital intermediaries. They move beyond traditional publisher regulation and seek to create a unified compliance framework covering:

  1. Social media intermediaries,
  2. AI-generated content,
  3. User-generated news and current affairs content, and
  4. Digital grievance redressal processes.

Although these amendments are not directly issued under the Digital Personal Data Protection Act, 2023 (DPDPA), they have important intersections with data governance:

  • Data retention obligations may interact with DPDPA provisions relating to storage limitation and legal exemptions.
  • AI-content labeling complements transparency principles relevant to responsible AI governance.
  • Expanded intermediary obligations strengthen accountability mechanisms within India’s broader digital governance framework.

Key Proposed Amendments

1. Mandatory Compliance with MeitY Directives

Social media intermediaries, including platforms such as X and Meta-operated services, will be required to comply with:

    • Clarifications
    • Advisories
    • Orders
    • Directions
    • Standard Operating Procedures (SOPs)
    • Codes of Practice
    • Guidelines

issued by MeitY.

Compliance with such directions will form part of the statutory “due diligence” obligations of intermediaries. Failure to comply could potentially affect the safe-harbour protections available under the Information Technology Act, 2000.

2. Enhanced AI-Generated Content Labeling Requirements

The amendment to Rule 3(3)(a)(ii) strengthens obligations relating to synthetic or AI-generated content.

Previous Requirement:

  • AI-generated content labels needed to be “prominently visible.”

Proposed Requirement:

  • Labels must be displayed continuously and clearly throughout the entire duration of the visual content.

Implication:

  • Platforms will need robust technical mechanisms to ensure persistent disclosure of AI-generated videos, images, and similar synthetic media.
  • The amendment reflects growing concerns regarding misinformation, deepfakes, and manipulated media.

3. Reinforcement of Data Retention Obligations

The amendments clarify that intermediaries must continue to comply with all legal requirements concerning:

    • Preservation of information
    • Retention of records
    • Maintenance of evidence

even when responding to user requests or regulatory actions.

Implication:

  • Data deletion requests cannot be used as a basis to circumvent statutory retention requirements.
  • This provision aligns with law-enforcement, regulatory, and evidentiary needs.

4. Expansion to User-Generated News and Current Affairs Content

A major policy shift is the inclusion of news and current affairs content uploaded by ordinary users.

Previously, regulatory obligations primarily targeted recognized digital publishers.

Under the proposed amendments:

  • User-generated news content may also fall within the regulatory framework.
  • Social media platforms hosting such content become subject to additional compliance responsibilities.

5. Strengthening of Grievance Redressal Mechanism

Rule 14 has been revised to strengthen the role of the Inter-Departmental Committee (IDC).

The IDC may:

  • Periodically hear complaints concerning violations of the Code of Ethics.
  • Consider cases where prescribed timelines have not been met.
  • Examine matters directly referred by MeitY.

6. Broader Applicability of Rules 14, 15 and 16

The amendment to Rule 8 extends the applicability of Rules 14, 15, and 16 beyond publishers.

These provisions will now apply to:

  • Publishers
  • Intermediaries
  • User-generated news and current affairs content hosted on intermediary platforms

Implication:

  • Regulatory accountability extends deeper into the social media ecosystem.
  • Platforms may bear greater responsibility for content generated by users.

The entire impact of the modified rule hinges on the definition of the “Synthetically generated information” which is defined as follows.

Rule 2 (wa) ‘synthetically generated information’ means audio, visual or audio-visual information which is artificially or algorithmically created, generated, modified or altered using a computer resource, in a manner that such information appears to be real, authentic or true and depicts or portrays any individual or event in a manner that is, or is likely to be perceived as indistinguishable from a natural person or real-world event;

Provided that the purposes of this clause, an audio, visual or audio-visual information shall not be deemed to be ‘synthetically generated information’, where such audio, visual or audio-visual information arises from—

(a) routine or good-faith editing, formatting, enhancement, technical correction, colour adjustment, noise reduction, transcription, or compression that does not materially alter, distort, or misrepresent the substance, context, or meaning of the underlying audio, visual or audio-visual information; or

(b) the routine or good-faith creation, preparation, formatting, presentation or design of documents, presentations, portable document format (PDF) files, educational or training materials, research outputs, including the use of illustrative, hypothetical, draft, template-based or conceptual content, where such creation or presentation does not result in the creation or generation of any false document or false electronic record; or

(c) the use of computer resources solely for improving accessibility, clarity, quality, translation, description, searchability, or discoverability, without generating, altering, or manipulating any material part of the underlying audio, visual or audio-visual information

Though the rule applies to all bloggers as indicated in the Indian Express Report,  there are sufficient safeguards to exclude routine bloggers who may use AI to create documents for educational or training materials without “depicting events as true events” which is normally done in You Tube videos covering events of news value.

Naavi

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DGPSI-Hospital ..framework for DPDPA Compliance in Hospitals taking shape

FDPPI has been a pioneer in designing a framework exclusively for compliance of DPDPA. The initial version of DGPSI incorporated the ITA 2000 and BIS draft guidelines on Data Governance and was born as a unified framework. With such a unification approach, DGPSI had become the  only framework suitable for the Indian data protection environment.

Subsequently with DGPSI-AI as an extension, the framework adopted the AI development in technology and today DGPSI-Full with DGPSI-AI stands tall amongst any such frameworks. It is suitable for implementation of DPDPA Compliance by default and is also certifiable by third party audit and also possesses ability to measure maturity of implementation through Data Trust Score (DTS).

Further DGPSI evolved with sector wise versions including DGPSI-HR, DGPSI-Data Processor and DGPSI-GDPR to meet specific requirements of HR, Data Processors and GDPR stake holders.

Time has come now to announce that a separate framework for the Hospital environment where there is a need for unification of “Patient Safety” requirements which  are presently handled under NABH  accreditation as a “Quality” criteria.

We started working on DGPSI-Health care as a framework. But it appears that there has to be a different framework for Hospitals under NABH guidelines from a framework for laboratories under NABL guidelines. We have  therefore decided to work presently on DGPSI-Hospital integrating the NABH quality requirements within the DGPSI framework.

Watch  out for more details …

Naavi

Listen here: The new  symbol of Trust

 

 

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