DPDP for a health-tech and telemedicine

Usually not for the treatment itself. A patient who comes for care gives data voluntarily for that purpose, and a medical emergency involving a threat to life is a listed use. Clinical consent for procedures is a separate medical and legal requirement and stays. Extra uses such as research, marketing, testimonials and sharing beyond what care and billing need do require DPDP consent.

Section 7(a) covers data given voluntarily for a specified purpose; Section 7(f) and 7(g) cover emergencies and epidemics. Section 7 · Section 6 · Section 5 · Rule 3

1. Keep clinical consent forms as they are.
2. Add a short notice at registration.
3. Add separate boxes for research, offers and stories.
4. Record which box each patient ticked.
5. Train front desk to explain the difference.

• Registration notice
• Consent records for extra uses

• One form that bundles treatment and marketing
• Calling clinical consent 'DPDP consent'
• No notice at registration

• What should our privacy notice say, and where must people see it?
• Can we use patient data for research, audits or case studies?
• Can we share patient records with insurers and TPAs?

Yes, for a claim the patient has asked for, because that is part of the purpose. Share only what the claim needs, through the TPA portal or a secure channel, and keep a record of what was sent. Sharing for anything else, such as an insurer's own marketing, needs consent.

Section 7(a) covers the claim purpose; Section 8(1) and 8(5) apply to how data is sent. Section 7 · Section 8(5) · Rule 6 · Sections 11–14 · Rule 14

1. Use TPA portals, not email.
2. Send only claim documents.
3. Log what was sent, to whom, when.
4. Answer patient questions about sharing.
5. Check TPA agreements.

• Sharing log
• TPA agreement

• Full case files by email
• No record of what was sent
• Insurer representatives reading records on wards

• Someone asks what data we hold about them. What do we send?
• What must a vendor contract say about personal data?
• Do we need DPDP consent to treat a patient?

Keep them for at least the periods health laws set: indoor records for three years from the start of treatment under the 2002 medical ethics regulations, PCPNDT records for two years, MTP registers for five years, Schedule H1 registers for three years, and ethics committee trial records for five years after a trial. Many hospitals keep records longer for continuity of care and legal claims. Write the period and reason for each record type, then erase or archive.

Section 8(7) allows retention where a law requires it; Rule 8(3) sets a one-year floor. Section 8(7) · Rule 8 · Section 7

1. List record types: OPD, IPD, lab, imaging, billing, PCPNDT, MTP, pharmacy.
2. Note the legal minimum.
3. Decide any longer period and why.
4. Archive with restricted access.
5. Record each deletion.

• Retention schedule
• Archive access list
• Deletion log

• No schedule at all
• Deleting before the minimum
• Keeping open access to old records

• How long can we keep personal data?
• Which records need extra protection under other health laws?
• Someone asks us to delete their data. Must we?

A notice must tell people, in plain words, what data you collect, why, how they can withdraw consent, how they can use their rights and how they can complain to the Data Protection Board. It has to stand on its own, separate from long terms and conditions, and be shown at the point where data is collected.

Registration desks, appointment apps, lab forms and health-camp sign-ups need short notices in the languages patients speak.

Section 5 and Rule 3 ask for a notice that can be understood on its own, with an itemised list of the data and the purpose for each item. Data you already hold from before the Act also needs a notice, as soon as reasonably practicable. Section 5 · Rule 3 · Section 6 · Sections 11–14 · Rule 14

1. List every point where personal data comes in: forms, apps, counters, calls, emails, partner feeds.
2. Write one short notice per collection point, with the data items and purpose side by side.
3. Add how to withdraw consent, how to make a request and the DPO or contact person's details.
4. Offer the notice in English and in the languages your app users actually use.
5. Keep each version with the date it went live.

• Screenshots or copies of the notice at each collection point, with dates
• Notice version history
• Translations, where used

• Hiding the notice inside terms and conditions
• One notice for everything, with no link between data items and purposes
• Forgetting old data collected before the Act

• When do we need consent, and when can we rely on a legitimate use?
• Someone withdraws consent. What has to stop, and how fast?
• Someone asks what data we hold about them. What do we send?

For every use of personal data you need one basis: consent, or one of the legitimate uses in Section 7, such as a legal duty, employment, a medical emergency, or data a person gave voluntarily for a specific purpose. Anything beyond what the person expects, such as marketing, profiling or sharing with partners, usually needs consent.

Treatment rests on the patient's purpose; research, offers and testimonials need consent.

Section 4 allows processing only with consent or for a legitimate use. Section 6 sets what valid consent looks like. Section 7 lists the uses that need no consent. Section 4 · Section 6 · Section 7

1. List each purpose for which you use personal data.
2. Against each purpose, write the basis: consent or the exact clause of Section 7.
3. Where the basis is consent, check that it was asked separately, with a clear action and no pre-ticked box.
4. Stop or re-paper any purpose with no basis.
5. Review the list whenever a new product, campaign or system starts.

• Purpose and basis register
• Consent records with date, version and channel
• Legal sign-off on each legitimate use relied on

• Treating account terms as consent for marketing
• Bundling several purposes in one tick-box
• Relying on 'legitimate interest', which the Indian Act does not have

• What should our privacy notice say, and where must people see it?
• Someone withdraws consent. What has to stop, and how fast?
• Can we send offers to past customers and leads?

Send a summary of the personal data you hold about them and what you do with it, and the names of the other organisations you shared it with and what was shared. Check the person's identity first, log the request and keep a copy of your reply.

Under the 2002 regulations, patients and authorised attendants should get record copies within 72 hours of a request. The DPDP summary adds who the data was shared with.

Section 11 gives the right to a summary and the list of organisations it was shared with. Rule 14 asks you to publish how requests are made and to answer within the period you publish. Sections 11–14 · Rule 14 · Section 8(9)–(10) · Rules 9, 14

1. Log the request in one register the day it arrives.
2. Verify identity using details you already hold.
3. Search every system, including vendors' copies.
4. Write a plain summary: what data, why it is used, who received it.
5. Send it, and file the request, search notes and reply.

• Request register
• Search notes for each request
• Copy of each reply with date

• Sending raw database dumps
• Forgetting data held by vendors
• No identity check before sending

• How do we handle a privacy complaint within 90 days?
• Someone asks us to delete their data. Must we?
• Where does personal data live in our organisation?