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Johnson & Johnson
Mankind Pharma
Adonis Phyto
Narang Biotec
Medanta
Redcliffe Labs
Sitaram Bhartia
Metro Hospitals
Tulasi Hospital
Bloom IVF
Milann
Prime IVF
MedLinks
Handa
Bhardwaj
Eye Q
Johnson & Johnson
Mankind Pharma
Adonis Phyto
Narang Biotec
Medanta
Redcliffe Labs
Sitaram Bhartia
Metro Hospitals
Tulasi Hospital
Bloom IVF
Milann
Prime IVF
MedLinks
Handa
Bhardwaj
Eye Q
Glossary · Compliance · Testimonial Rules

Patient Testimonial Consent requires written, purpose-limited, revocable consent per testimonial per intended use — under DPDP Act 2023 and profession codes.

Patient Testimonial Consent is the specific consent regime for using patient testimonials in Indian healthcare marketing. Governed by DPDP Act 2023, NMC Code of Ethics 2023, and profession-specific codes (DCI for dental, NABH for accredited hospitals), it requires written, purpose-limited, revocable consent per testimonial per intended use.

Mechanism

How it works.

  1. Use a specific-purpose consent form per testimonial. Not a blanket release.
  2. Specify intended channels in scope. Website, Instagram, Meta ads, brochure — each named.
  3. Specify duration. Typically 3-5 years; renewable with fresh consent.
  4. Disclose compensation if any. Consent form and the published testimonial both disclose.
  5. Store consent evidence per testimonial per patient. Retrievable within minutes on request.
  6. Process withdrawals within 7 days. Remove material from all channels.
Why it matters

Why it matters for
Indian healthcare.

Patient testimonials are one of the most powerful marketing formats in Indian healthcare — and one of the most heavily regulated. The regulation stacks: DPDP Act 2023 (consent), NMC 2023 (doctor-patient conduct), profession-specific codes (DCI for dental, NABH for accredited hospitals, ART Act 2021 for fertility), Magic Remedies Act (54-disease outcome-claim prohibition), and ASCI (advertising code). Any testimonial has to satisfy every applicable layer. Dental testimonials effectively cannot reference outcomes at all (DCI/AAP). Fertility testimonials cannot make success-rate claims outside NARC-substantiated ranges (ART Act). ICG treats testimonial production as a compliance-first workflow — the concept starts inside the constraint set, not with a beautiful story that fails review.

Inside the ICG stack

How ICG uses this.

ICG maintains a testimonial consent library aligned to DPDP Act 2023, NMC 2023, and each profession-specific overlay. The workflow captures consent, stores evidence, and processes withdrawals within the 7-day operational standard. Related: Consent Form (Marketing Usage), DPDP Consent (Healthcare), AAP Testimonial Ban.

FAQ

Frequently asked questions.

Is a general release form enough?

No — DPDP Act 2023 requires purpose-limited consent. A general "you may use my info" release does not meet the standard. Each testimonial and each intended usage (Instagram, website, brochure) needs specific consent scope.

Can a minor patient consent?

No — minors' testimonial consent must be captured from parent/legal guardian under DPDP Act 2023 Section 9, with additional restrictions on marketing use.

What if the patient later withdraws consent?

The clinic must remove the testimonial from circulation within a reasonable window (7 days is the ICG operational standard). Withdrawal-processing capability is a DPDP compliance requirement.

Are compensated testimonials permitted?

Compensation is a material disclosure — the testimonial must disclose the compensation clearly. NMC 2023 further restricts compensated doctor-patient endorsements. ASCI guidelines require clear disclosure of any material connection.

Set up testimonial consent
aligned to DPDP Act 2023.

ICG runs a free 30-min Brand & Growth Diagnostic that plugs into your live account and surfaces this metric against portfolio benchmarks.

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